Aktuelle Ernährungsmedizin 2015; 40(05): e1-e74
DOI: 10.1055/s-0035-1552741
Leitlinie
© Georg Thieme Verlag KG Stuttgart · New York

S3-Leitline der Deutschen Gesellschaft für Ernährungsmedizin e. V. (DGEM) in Kooperation mit der Deutschen Gesellschaft für Hämatologie und Onkologie e. V. (DGHO), der Arbeitsgemeinschaft „Supportive Maßnahmen in der Onkologie, Rehabilitation und Sozialmedizin“ der Deutschen Krebsgesellschaft (ASORS) und der Österreichischen Arbeitsgemeinschaft für klinische Ernährung (AKE)

Klinische Ernährung in der OnkologieS3-Guideline of the German Society for Nutritional Medicine (DGEM) in Cooperation with the DGHO, the ASORS and the AKEClinical Nutrition in Oncology
J. Arends
1   Klinik für Tumorbiologie, Freiburg im Breisgau
,
H. Bertz
2   Klinik Innere Medizin I, Universitätsklinik, Hämatologie/Onkologie/Stammzelltransplantation, Sektion Ernährungsmedizin, Freiburg
,
S. C. Bischoff
3   Institut für Ernährungsmedizin, Universität Hohenheim, Stuttgart
,
R. Fietkau
4   Strahlenklinik, Universitätsklinikum Erlangen
,
H. J. Herrmann
5   Klinische und Experimentelle Ernährungsmedizin, Medizinische Klinik 1, Universitätsklinikum Erlangen
,
E. Holm
6   Universitätsklinikum Mannheim
,
M. Horneber
7   Klinik für Innere Medizin 5, Schwerpunkt Onkologie/Hämatologie, Paracelsus Medizinische Privatuniversität, Klinikum Nürnberg
,
E. Hütterer
8   Universitätsklinik für Innere Med. I, Onkologie 6i, Wien
,
J. Körber
9   Hamm-Kliniken GmbH & Co. KG, Klinik Nahetal, Bad Kreuznach
,
I. Schmid
10   Dr. von Haunersches Kinderspital, Klinikum der Universität München
,
und das DGEM Steering Committee › Institutsangaben
Weitere Informationen

Publikationsverlauf

Publikationsdatum:
02. November 2015 (online)

Zusammenfassung

Fragestellung: Bei Tumorpatienten führen sowohl erkrankungs- als auch therapieassoziierte Belastungen häufig zu einer Mangelernährung. Zentrale klinische Probleme sind eine unzureichende Nahrungsaufnahme, eine Einschränkung der körperlichen Aktivität und Mobilität sowie katabole metabolische Veränderungen im Sinne einer systemischen Inflammationsreaktion, die oft gemeinsam vorliegen. Diese Leitlinie soll evidenzbasierte Empfehlungen zur Erkennung und ggf. multimodalen Behandlung von Ernährungs- und Stoffwechselstörungen bei Tumorpatienten geben.

Methodik: Es wurden eine systematische Literaturrecherche sowie eine Handsuche zu Literatur über Ernährungs- und Stoffwechelstörungen bei Tumorpatienten durchgeführt. Die Ergebnisse wurden in einer interdisziplinären Arbeitsgruppe aus Ärzten, Ernährungswissenschaftlern und Diätassistenten diskutiert und bewertet. Auf dieser Basis wurden von der Arbeitsgruppe Empfehlungen erarbeitet, die auf der Konsensuskonferenz am 18. und 19. Oktober 2013 vorgestellt, diskutiert, z. T. modifiziert und verabschiedet wurden.

Ergebnisse: Die Leitlinie enthält 48 Empfehlungen zur klinischen Ernährung in der Onkologie. Zur frühzeitigen Erfassung von Ernährungsstörungen sollen valide Screeningverfahren eingesetzt und bei Auffälligkeiten im Screening durch ein gezieltes Assessment ergänzt werden. Grundsätzlich soll eine ausreichende Energie- und Eiweißzufuhr gesichert werden. Hierzu eignen sich die Linderung ernährungsrelevanter Symptome sowie ein der individuellen Situation angemessener Einsatz professioneller Ernährungsberatung inkl. oraler bilanzierter Diäten (Trinknahrungen), Sondenernährung bzw. intravenöser Ernährung. Jede Ernährungsbetreuung sollte zum Aufbau der Muskelmasse von bewegungstherapeutischen Maßnahmen begleitet werden. Bei Patienten mit fortgeschrittener Erkrankung können medikamentöse Substanzen zur Steigerung des Appetits, zur Vergrößerung der Muskelmasse und zur Minderung der Inflammationsreaktion erwogen werden. Während einer Bestrahlung im Kopf-Hals-Bereich ist frühzeitig der Einsatz von Trinknahrungen und ggf. einer Sondenernährung in Betracht zu ziehen, um den Energiebedarf zu sichern und eine Unterbrechung der Bestrahlung zu verhindern. Während einer medikamentösen Tumorbehandlung gilt analog, dass eine ausreichende Nahrungszufuhr gesichert werden soll, ggf. unter Anwendung einer enteralen und/oder parenteralen Nahrungszufuhr. Nach kurativer Tumorbehandlung werden regelmäßige körperliche Aktivität sowie eine die Bedarfsdeckung nicht übersteigende Energiezufuhr empfohlen. Abhängig von der Erkrankungsprognose sollte auch bei unheilbar kranken Tumorpatienten auf eine ausreichende Nahrungsaufnahme geachtet werden, während in der Sterbephase die Zufuhr von Nahrung und Flüssigkeit allein symptomorientiert erfolgen soll.

Schlussfolgerung: Durchgehende Aufmerksamkeit für mögliche Ernährungsstörungen sowie eine der jeweiligen Situation angemessene Ernährungsbehandlung sollen Teil der Supportivbetreuung jedes Tumorpatienten sein, um die Körperreserven, die Therapietoleranz, den Erkrankungsverlauf und die Lebensqualität günstig zu beeinflussen.

Abstract

Aim: In cancer patients, tumor- and treatment-associated factors may promote malnutrition. Inadequate food intake, diminished physical activity and metabolic catabolic derangements (systemic inflammation) are major clinical problems; they are often present simultaneously. This guideline presents evidence-based recommendations for detection and multi-modal treatment of nutritional and metabolic problems in cancer patients.

Methods: This guideline is based on a systematic literature search and hand-searches of relevant literature by experts. Results were discussed and evaluated by a group of physicians, nutritionists and dieticians. Clinical recommendations derived by the group were presented, discussed, adapted and finally adopted during a consensus conference on 18 – 19 October 2013.

Results: This guideline is composed of 48 recommendations dealing with clinical nutrition in cancer patients. To detect nutritional problems early, we recommend screening for malnutrition in all cancer patients; abnormal screening should be followed by dedicated nutrition assessment. Generally, an adequate intake of energy and protein should be ensured. This may be achieved by treatment of nutrition impact symptoms and the appropriate and if necessary escalating use of nutrition counseling, oral nutritional supplements (ONS), tube feedings and/or intravenous nutrition. To improve muscle mass, nutritional care should always be accompanied by exercise training. In patients with advanced cancer, pharmacological agents may be considered to improve appetite, muscle mass and systemic inflammation. During radiotherapy of head and neck cancers the appropriate use of ONS or tube feedings should not be missed to ensure continuity of an adequate energy intake and to avoid interruptions of the treatment. Similarly, during anticancer drug treatment an adequate provision of energy should be ensured, if necessary by applying nutrition by enteral or parenteral routes. Cancer survivors should be physically active and balance energy intake with requirements. Depending on life expectancy, also in incurable cancer patients an adequate nutritional supply should be provided. However, during the dying phase nutrition and fluids should only be supplied as required to alleviate symptoms.

Conclusion: Supportive care of all cancer patients should always include continuous attention to potential nutritional problems and if necessary early and adequate nutritional support. This is aimed at improving body resources, the tolerance of anticancer treatments, the overall prognosis and the patients’ quality of life.

* DGEM Steering Committee: Bischoff SC, Weimann A, Adolph M, Normann K, Plauth M, Ockenga J.


 
  • Literaturverzeichnis

  • 1 Arends J, Zürcher G, Fietkau R et al. DGEM-Leitlinien Enterale Ernährung: Onkologie. Aktuel Ernahrungsmed 2003; 28: 61-68
  • 2 Arends J, Dossett A, Fietkau R et al. Nichtchirurgische Onkologie. Aktuel Ernahrungsmed 2007; 32: S124-S133
  • 3 Stingel K, Schütz T, Koller M et al. Leitlinie der Deutschen Gesellschaft für Ernährungsmedizin (DGEM) – Methodik zum Leitlinien-Update Klinische Ernährung. Aktuel Ernahrungsmed 2013; 38: 90-96
  • 4 Ravasco P, Monteiro-Grillo I, Vidal PM et al. Cancer: disease and nutrition are key determinants of patients’ quality of life. Support Care Cancer 2004; 12: 246-252
  • 5 Bosaeus I, Daneryd P, Svanberg E et al. Dietary intake and resting energy expenditure in relation to weight loss in unselected cancer patients. Int J Cancer 2001; 93: 380-383
  • 6 Deans DA, Tan BH, Wigmore SJ et al. The influence of systemic inflammation, dietary intake and stage of disease on rate of weight loss in patients with gastro-oesophageal cancer. Br J Cancer 2009; 100: 63-69
  • 7 Dewys WD, Begg C, Lavin PT et al. Prognostic effect of weight loss prior to chemotherapy in cancer patients. Eastern Cooperative Oncology Group. Am J Med 1980; 69: 491-497
  • 8 Andreyev HJ, Norman AR, Oates J et al. Why do patients with weight loss have a worse outcome when undergoing chemotherapy for gastrointestinal malignancies?. Eur J Cancer 1998; 34: 503-509
  • 9 Bozzetti F, Arends J, Lundholm K et al. ESPEN Guidelines on Parenteral Nutrition: non-surgical oncology. Clin Nutr 2009; 28: 445-454
  • 10 Attar A, Malka D, Sabate JM et al. Malnutrition is high and underestimated during chemotherapy in gastrointestinal cancer: an AGEO prospective cross-sectional multicenter study. Nutr Cancer 2012; 64: 535-542
  • 11 Lynch GS, Schertzer JD, Ryall JG. Therapeutic approaches for muscle wasting disorders. Pharmacol Ther 2007; 113: 461-487
  • 12 Fearon K, Arends J, Baracos V. Understanding the mechanisms and treatment options in cancer cachexia. Nat Rev Clin Oncol 2013; 10: 90-99
  • 13 Bozzetti F. Nutritional support in patients with oesophageal cancer. Support Care Cancer 2010; 18 (Suppl. 02) S41-S50
  • 14 Brocca L, Cannavino J, Coletto L et al. The time course of the adaptations of human muscle proteome to bed rest and the underlying mechanisms. J Physiol 2012; 590: 5211-5230
  • 15 Ferriolli E, Skipworth RJ, Hendry P et al. Physical activity monitoring: a responsive and meaningful patient-centered outcome for surgery, chemotherapy, or radiotherapy?. J Pain Symptom Manage 2012; 43: 1025-1035
  • 16 Prado CM, Lieffers JR, McCargar LJ et al. Prevalence and clinical implications of sarcopenic obesity in patients with solid tumours of the respiratory and gastrointestinal tracts: a population-based study. Lancet Oncol 2008; 9: 629-635
  • 17 Baracos V, Kazemi-Bajestani SM. Clinical outcomes related to muscle mass in humans with cancer and catabolic illnesses. Int J Biochem Cell Biol 2013; 45: 2302-2308
  • 18 Fearon K, Strasser F, Anker SD et al. Definition and classification of cancer cachexia: an international consensus. Lancet Oncol 2011; 12: 489-495
  • 19 Jensen GL, Mirtallo J, Compher C et al. Adult starvation and disease-related malnutrition: a proposal for etiology-based diagnosis in the clinical practice setting from the International Consensus Guideline Committee. JPEN J Parenter Enteral Nutr 2010; 34: 156-159
  • 20 Arends J. Mangelernährung bei Tumorpatienten. Onkologe 2008; 14: 9-14
  • 21 Fearon KC, Voss AC, Hustead DS. Cancer Cachexia Study Group. Definition of cancer cachexia: effect of weight loss, reduced food intake, and systemic inflammation on functional status and prognosis. Am J Clin Nutr 2006; 83: 1345-1350
  • 22 Morley JE, Thomas DR, Wilson MM. Cachexia: pathophysiology and clinical relevance. Am J Clin Nutr 2006; 83: 735-743
  • 23 Evans WJ, Morley JE, Argiles J et al. Cachexia: a new definition. Clin Nutr 2008; 27: 793-799
  • 24 Muscaritoli M, Anker SD, Argiles J et al. Consensus definition of sarcopenia, cachexia and pre-cachexia: joint document elaborated by Special Interest Groups (SIG) “cachexia-anorexia in chronic wasting diseases” and “nutrition in geriatrics”. Clin Nutr 2010; 29: 154-159
  • 25 McMillan DC. The systemic inflammation-based Glasgow Prognostic Score: a decade of experience in patients with cancer. Cancer Treat Rev 2013; 39: 534-540
  • 26 Deans C, Wigmore SJ. Systemic inflammation, cachexia and prognosis in patients with cancer. Curr Opin Clin Nutr Metab Care 2005; 8: 265-269
  • 27 Jamieson NB, Glen P, McMillan DC et al. Systemic inflammatory response predicts outcome in patients undergoing resection for ductal adenocarcinoma head of pancreas. Br J Cancer 2005; 92: 21-23
  • 28 Skipworth RJ, Stewart GD, Dejong CH et al. Pathophysiology of cancer cachexia: much more than host-tumour interaction?. Clin Nutr 2007; 26: 667-676
  • 29 Oehmichen F, Ballmer PE, Druml C et al. Leitlinie der Deutschen Gesellschaft für Ernährungsmedizin (DGEM) – Ethische und rechtliche Gesichtspunkte der Künstlichen Ernährung. Aktuel Ernahrungsmed 2013; 38: 112-117
  • 30 Bozzetti F, Mori V. Nutritional support and tumour growth in humans: a narrative review of the literature. Clin Nutr 2009; 28: 226-230
  • 31 Jin D, Phillips M, Byles JE. Effects of parenteral nutrition support and chemotherapy on the phasic composition of tumor cells in gastrointestinal cancer. JPEN J Parenter Enteral Nutr 1999; 23: 237-241
  • 32 Cao WX, Xiao HB, Yin HR. Effects of preoperative parenteral nutritional support with chemotherapy on tumor cell kinetics in gastric cancer patients. Zhonghua Zhong Liu Za Zhi 1994; 16: 137-140
  • 33 Valentini L. Leitlinie der Deutschen Gesellschaft für Ernährungsmedizin (DGEM): DGEM-Terminologie in der Klinischen Ernährung. Aktuel Ernahrungsmed 2013; 38: 97-111
  • 34 Meijers JM, Halfens RJ, Mijnarends DM et al. A feedback system to improve the quality of nutritional care. Nutrition 2013; 29: 1037-1041
  • 35 Meijers JM, Tan F, Schols JM et al. Nutritional care; do process and structure indicators influence malnutrition prevalence over time?. Clin Nutr 2014; 33: 459-465
  • 36 Correia MI, Hegazi RA, Higashiguchi T et al. Evidence-based recommendations for addressing malnutrition in health care: an updated strategy from the feedM.E. Global Study Group. J Am Med Dir Assoc 2014; 15: 544-550
  • 37 Kris-Etherton PM, Akabas SR, Douglas P et al. Nutrition competencies in health professionals’ education and training: a new paradigm. Adv Nutr 2015; 6: 83-87
  • 38 Starke J, Schneider H, Alteheld B et al. Short-term individual nutritional care as part of routine clinical setting improves outcome and quality of life in malnourished medical patients. Clin Nutr 2011; 30: 194-201
  • 39 Lacey K, Pritchett E. Nutrition Care Process and Model: ADA adopts road map to quality care and outcomes management. J Am Diet Assoc 2003; 103: 1061-1072
  • 40 Buchholz D, Ohlrich S. Der Nutrition Care Process. D&I 2011; 5: 10-15
  • 41 Lee HO, Lee JJ. Nutritional intervention using nutrition care process in a malnourished patient with chemotherapy side effects. Clin Nutr Res 2015; 4: 63-67
  • 42 Odelli C, Burgess D, Bateman L et al. Nutrition support improves patient outcomes, treatment tolerance and admission characteristics in oesophageal cancer. Clin Oncol (R Coll Radiol) 2005; 17: 639-645
  • 43 Bozzetti F, Mariani L, Lo Vullo S et al. SCRINIO Working Group. The nutritional risk in oncology: a study of 1,453 cancer outpatients. Support Care Cancer 2012; 20: 1919-1928
  • 44 Gavazzi C, Colatruglio S, Sironi A et al. Importance of early nutritional screening in patients with gastric cancer. Br J Nutr 2011; 106: 1773-1778
  • 45 Kondrup J, Allison SP, Elia M et al. ESPEN guidelines for nutrition screening 2002. Clin Nutr 2003; 22: 415-421
  • 46 Ryu SW, Kim IH. Comparison of different nutritional assessments in detecting malnutrition among gastric cancer patients. World J Gastroenterol 2010; 16: 3310-3317
  • 47 Gupta D, Vashi PG, Lammersfeld CA et al. Role of nutritional status in predicting the length of stay in cancer: a systematic review of the epidemiological literature. Ann Nutr Metab 2011; 59: 96-106
  • 48 Stratton RJ, Hackston A, Longmore D et al. Malnutrition in hospital outpatients and inpatients: prevalence, concurrent validity and ease of use of the 'malnutrition universal screening tool' ('MUST') for adults. Br J Nutr 2004; 92: 799-808
  • 49 Ottery FD. Definition of standardized nutritional assessment and interventional pathways in oncology. Nutrition 1996; 12: S15-S19
  • 50 Bauer J, Capra S, Ferguson M. Use of the scored Patient-Generated Subjective Global Assessment (PG-SGA) as a nutrition assessment tool in patients with cancer. Eur J Clin Nutr 2002; 56: 779-785
  • 51 Thibault R, Goujon N, Le Gallic E et al. Use of 10-point analogue scales to estimate dietary intake: a prospective study in patients nutritionally at-risk. Clin Nutr 2009; 28: 134-140
  • 52 Bjornsdottir R, Oskarsdottir ES, Thordardottir FR et al. Validation of a plate diagram sheet for estimation of energy and protein intake in hospitalized patients. Clin Nutr 2013; 32: 746-751
  • 53 Omlin A, Blum D, Wierecky J et al. Nutrition impact symptoms in advanced cancer patients: frequency and specific interventions, a case-control study. J Cachexia Sarcopenia Muscle 2013; 4: 55-61
  • 54 Walsh D, Mahmoud F, Barna B. Assessment of nutritional status and prognosis in advanced cancer: interleukin-6, C-reactive protein, and the prognostic and inflammatory nutritional index. Support Care Cancer 2003; 11: 60-62
  • 55 Nitenberg G, Raynard B. Nutritional support of the cancer patient: issues and dilemmas. Crit Rev Oncol Hematol 2000; 34: 137-168
  • 56 Epstein JB, Barasch A. Taste disorders in cancer patients: pathogenesis, and approach to assessment and management. Oral Oncol 2010; 46: 77-81
  • 57 Tong H, Isenring E, Yates P. The prevalence of nutrition impact symptoms and their relationship to quality of life and clinical outcomes in medical oncology patients. Support Care Cancer 2009; 17: 83-90
  • 58 Farrell C, Brearley SG, Pilling M et al. The impact of chemotherapy-related nausea on patients’ nutritional status, psychological distress and quality of life. Support Care Cancer 2013; 21: 59-66
  • 59 Henson CC, Burden S, Davidson SE et al. Nutritional interventions for reducing gastrointestinal toxicity in adults undergoing radical pelvic radiotherapy. Cochrane Database Syst Rev 2013; 11 CD009896
  • 60 Wang-Gillam A, Abrams RA, Posner MC et al. Supportive care considerations during concurrent chemoradiotherapy for pancreatic adenocarcinoma: lessons learned from clinical experience. Am J Clin Oncol 2013; 36: 637-643
  • 61 Hopkinson JB. Psychosocial impact of cancer cachexia. J Cachexia Sarcopenia Muscle 2014; 5: 89-94
  • 62 Prado CM, Baracos VE, McCargar LJ et al. Sarcopenia as a determinant of chemotherapy toxicity and time to tumor progression in metastatic breast cancer patients receiving capecitabine treatment. Clin Cancer Res 2009; 15: 2920-2926
  • 63 Jang RW, Caraiscos VB, Swami N et al. Simple prognostic model for patients with advanced cancer based on performance status. J Oncol Pract 2014; 10: e335-e341
  • 64 Oken MM, Creech RH, Tormey DC et al. Toxicity and response criteria of the Eastern Cooperative Oncology Group. Am J Clin Oncol 1982; 5: 649-655
  • 65 Shen W, Punyanitya M, Wang Z et al. Total body skeletal muscle and adipose tissue volumes: estimation from a single abdominal cross-sectional image. J Appl Physiol (1985) 2004; 97: 2333-2338
  • 66 Mourtzakis M, Prado CM, Lieffers JR et al. A practical and precise approach to quantification of body composition in cancer patients using computed tomography images acquired during routine care. Appl Physiol Nutr Metab 2008; 33: 997-1006
  • 67 Martin L, Birdsell L, Macdonald N et al. Cancer cachexia in the age of obesity: skeletal muscle depletion is a powerful prognostic factor, independent of body mass index. J Clin Oncol 2013; 31: 1539-1547
  • 68 Yip C, Goh V, Davies A et al. Assessment of sarcopenia and changes in body composition after neoadjuvant chemotherapy and associations with clinical outcomes in oesophageal cancer. Eur Radiol 2014; 24: 998-1005
  • 69 Jackson W, Alexander N, Schipper M et al. Characterization of changes in total body composition for patients with head and neck cancer undergoing chemoradiotherapy using dual-energy x-ray absorptiometry. Head Neck 2014; 36: 1356-1362
  • 70 Heymsfield SB, Adamek M, Gonzalez MC et al. Assessing skeletal muscle mass: historical overview and state of the art. J Cachexia Sarcopenia Muscle 2014; 5: 9-18
  • 71 Janssen I, Heymsfield SB, Baumgartner RN et al. Estimation of skeletal muscle mass by bioelectrical impedance analysis. J Appl Physiol (1985) 2000; 89: 465-471
  • 72 Christensen JF, Jones LW, Andersen JL et al. Muscle dysfunction in cancer patients. Ann Oncol 2014; 25: 947-958
  • 73 Pitta F, Troosters T, Probst VS et al. Quantifying physical activity in daily life with questionnaires and motion sensors in COPD. Eur Respir J 2006; 27: 1040-1055
  • 74 Norman K, Stobäus N, Lochs H et al. Messung der Muskelkraft als ernährungsmedizinische Zielgröße. Aktuel Ernahrungsmed 2009; 34: 263-268
  • 75 Mauricio SF, da Silva JB, Bering T et al. Relationship between nutritional status and the Glasgow Prognostic Score in patients with colorectal cancer. Nutrition 2013; 29: 625-629
  • 76 da Silva JB, Mauricio SF, Bering T et al. The relationship between nutritional status and the Glasgow prognostic score in patients with cancer of the esophagus and stomach. Nutr Cancer 2013; 65: 25-33
  • 77 Laird BJ, Kaasa S, McMillan DC et al. Prognostic factors in patients with advanced cancer: a comparison of clinicopathological factors and the development of an inflammation-based prognostic system. Clin Cancer Res 2013; 19: 5456-5464
  • 78 Richards CH, Roxburgh CS, MacMillan MT et al. The relationships between body composition and the systemic inflammatory response in patients with primary operable colorectal cancer. PLoS One 2012; 7: e41883
  • 79 Proctor MJ, Morrison DS, Talwar D et al. An inflammation-based prognostic score (mGPS) predicts cancer survival independent of tumour site: a Glasgow Inflammation Outcome Study. Br J Cancer 2011; 104: 726-734
  • 80 Deutsche Gesellschaft für Ernährung, Österreichische Gesellschaft für Ernährung, Schweizerische Gesellschaft für Ernährung. Referenzwerte für Nährstoffzufuhr – praktische Loseblattsammlung. 2nd. ed., Deutsche Gesellschaft für Ernährung; 2015
  • 81 Kreymann KG, de Heer G, Felbinger T et al. Nutrition of critically ill patients in intensive care. Internist (Berl) 2007; 48: 1084-1092
  • 82 Holm E. Stoffwechsel und Ernährung bei Tumorkrankheiten: Analysen und Empfehlungen. 1st. ed., Thieme; 2007
  • 83 Bertz H, Zürcher G. Ernährung in der Onkologie: Grundlagen und klinische Praxis. 1st. ed., Schattauer; 2014
  • 84 Knasmüller S. Krebs und Ernährung. 1st. ed., Thieme; 2014
  • 85 Brandhorst S, Wei M, Hwang S et al. Short-term calorie and protein restriction provide partial protection from chemotoxicity but do not delay glioma progression. Exp Gerontol 2013; 48: 1120-1128
  • 86 Shim HS, Wei M, Brandhorst S et al. Starvation Promotes REV1 SUMOylation and p53-Dependent Sensitization of Melanoma and Breast Cancer Cells. Cancer Res 2015; 75: 1056-1067
  • 87 Kulstad R, Schoeller DA. The energetics of wasting diseases. Curr Opin Clin Nutr Metab Care 2007; 10: 488-493
  • 88 Knox LS, Crosby LO, Feurer ID et al. Energy expenditure in malnourished cancer patients. Ann Surg 1983; 197: 152-162
  • 89 Dempsey DT, Knox LS, Mullen JL et al. Energy expenditure in malnourished patients with colorectal cancer. Arch Surg 1986; 121: 789-795
  • 90 Jatoi A, Daly BD, Hughes VA et al. Do patients with nonmetastatic non-small cell lung cancer demonstrate altered resting energy expenditure?. Ann Thorac Surg 2001; 72: 348-351
  • 91 Moses AW, Slater C, Preston T et al. Reduced total energy expenditure and physical activity in cachectic patients with pancreatic cancer can be modulated by an energy and protein dense oral supplement enriched with n-3 fatty acids. Br J Cancer 2004; 90: 996-1002
  • 92 Lieffers JR, Mourtzakis M, Hall KD et al. A viscerally driven cachexia syndrome in patients with advanced colorectal cancer: contributions of organ and tumor mass to whole-body energy demands. Am J Clin Nutr 2009; 89: 1173-1179
  • 93 Energy and protein requirements. Report of a joint FAO/WHO/UNU Expert Consultation. World Health Organ Tech Rep Ser 1985; 724: 1-206
  • 94 Schofield WN. Predicting basal metabolic rate, new standards and review of previous work. Hum Nutr Clin Nutr 1985; 39 (Suppl. 01) 5-41
  • 95 Roza AM, Shizgal HM. The Harris Benedict equation reevaluated: resting energy requirements and the body cell mass. Am J Clin Nutr 1984; 40: 168-182
  • 96 Bencini L, Di Leo A, Pozzessere D et al. Total energy expenditure in patients with advanced solid tumours: a preliminary report. Nutritional Therapy & Metabolism 2008; 26: 25-47
  • 97 Cereda E, Turrini M, Ciapanna D et al. Assessing energy expenditure in cancer patients: a pilot validation of a new wearable device. JPEN J Parenter Enteral Nutr 2007; 31: 502-507
  • 98 Schoeller DA, van Santen E. Measurement of energy expenditure in humans by doubly labeled water method. J Appl Physiol Respir Environ Exerc Physiol 1982; 53: 955-959
  • 99 Westerterp KR. Physical activity, food intake, and body weight regulation: insights from doubly labeled water studies. Nutr Rev 2010; 68: 148-154
  • 100 Arends J, Bodoky G, Bozzetti F et al. ESPEN Guidelines on Enteral Nutrition: Non-surgical oncology. Clin Nutr 2006; 25: 245-259
  • 101 Kreymann G, Adolph A, Druml W et al. Intensivmedizin. Aktuel Ernahrungsmed 2007; 32: S89-S92
  • 102 Heber D, Chlebowski RT, Ishibashi DE et al. Abnormalities in glucose and protein metabolism in noncachectic lung cancer patients. Cancer Res 1982; 42: 4815-4819
  • 103 Shaw JH, Humberstone DM, Wolfe RR. Energy and protein metabolism in sarcoma patients. Ann Surg 1988; 207: 283-289
  • 104 Guadagni M, Biolo G. Effects of inflammation and/or inactivity on the need for dietary protein. Curr Opin Clin Nutr Metab Care 2009; 12: 617-622
  • 105 Elango R, Humayun MA, Ball RO et al. Evidence that protein requirements have been significantly underestimated. Curr Opin Clin Nutr Metab Care 2010; 13: 52-57
  • 106 Deutz NE, Bauer JM, Barazzoni R et al. Protein intake and exercise for optimal muscle function with aging: recommendations from the ESPEN Expert Group. Clin Nutr 2014; 33: 929-936
  • 107 Bauer J, Biolo G, Cederholm T et al. Evidence-based recommendations for optimal dietary protein intake in older people: a position paper from the PROT-AGE Study Group. J Am Med Dir Assoc 2013; 14: 542-559
  • 108 Haran PH, Rivas DA, Fielding RA. Role and potential mechanisms of anabolic resistance in sarcopenia. J Cachexia Sarcopenia Muscle 2012; 3: 157-162
  • 109 Winter A, MacAdams J, Chevalier S. Normal protein anabolic response to hyperaminoacidemia in insulin-resistant patients with lung cancer cachexia. Clin Nutr 2012; 31: 765-773
  • 110 Bozzetti F, Bozzetti V. Is the intravenous supplementation of amino acid to cancer patients adequate? A critical appraisal of literature. Clin Nutr 2013; 32: 142-146
  • 111 Martin WF, Armstrong LE, Rodriguez NR. Dietary protein intake and renal function. Nutr Metab (Lond) 2005; 2: 25
  • 112 Druml W, Contzen B, Joannidis M et al. S1-Leitlinie der Deutschen Gesellschaft für Ernährungsmedizin (DGEM) in Zusammenarbeit mit der AKE, der GESKES und der DGfN: Enterale und parenterale Ernährung von Patienten mit Niereninsuffizienz. Aktuel Ernahrungsmed 2015; 40: 21-37
  • 113 Bozzetti F, Gavazzi C, Mariani L et al. Glucose-based total parenteral nutrition does not stimulate glucose uptake by humans tumours. Clin Nutr 2004; 23: 417-421
  • 114 Holm E, Kämmerer U. Fette und Kohlenhydrate in Ernährungskonzepten für Tumorpatienten. Aktuel Ernahrungsmed 2011; 36: 286-298
  • 115 Breitkreutz R, Tesdal K, Jentschura D et al. Effects of a high-fat diet on body composition in cancer patients receiving chemotherapy: a randomized controlled study. Wien Klin Wochenschr 2005; 117: 685-692
  • 116 Bassler KH. Significance of vitamins in parenteral nutrition. Infusionstherapie 1990; 17: 19-23
  • 117 Bassler KH. German Study Group for Artificial Nutrition. Recommendations for administration of trace elements in parenteral feeding of adults. Infusionstherapie 1990; 17: 283
  • 118 Shenkin A. The key role of micronutrients. Clin Nutr 2006; 25: 1-13
  • 119 Biesalski HK, Bischoff SC, Böhles H et al. Wasser, Elektrolyte, Vitamine und Spurenelemente. Aktuel Ernahrungsmed 2007; 32: S30-S34
  • 120 Giovannucci E, Chan AT. Role of vitamin and mineral supplementation and aspirin use in cancer survivors. J Clin Oncol 2010; 28: 4081-4085
  • 121 Mamede AC, Tavares SD, Abrantes AM et al. The role of vitamins in cancer: a review. Nutr Cancer 2011; 63: 479-494
  • 122 Strohle A, Zanker K, Hahn A. Nutrition in oncology: the case of micronutrients (review). Oncol Rep 2010; 24: 815-828
  • 123 Luczynska A, Kaaks R, Rohrmann S et al. Plasma 25-hydroxyvitamin D concentration and lymphoma risk: results of the European Prospective Investigation into Cancer and Nutrition. Am J Clin Nutr 2013; 98: 827-838
  • 124 Drake MT, Maurer MJ, Link BK et al. Vitamin D insufficiency and prognosis in non-Hodgkin’s lymphoma. J Clin Oncol 2010; 28: 4191-4198
  • 125 Arends J. Vitamin D in oncology. Forsch Komplementmed 2011; 18: 176-184
  • 126 Zgaga L, Theodoratou E, Farrington SM et al. Plasma vitamin D concentration influences survival outcome after a diagnosis of colorectal cancer. J Clin Oncol 2014; 32: 2430-2439
  • 127 Akutsu Y, Kono T, Uesato M et al. Are additional trace elements necessary in total parenteral nutrition for patients with esophageal cancer receiving cisplatin-based chemotherapy?. Biol Trace Elem Res 2012; 150: 109-115
  • 128 Isenring EA, Capra S, Bauer JD. Nutrition intervention is beneficial in oncology outpatients receiving radiotherapy to the gastrointestinal or head and neck area. Br J Cancer 2004; 91: 447-452
  • 129 Ravasco P, Monteiro-Grillo I, Marques Vidal P et al. Impact of nutrition on outcome: a prospective randomized controlled trial in patients with head and neck cancer undergoing radiotherapy. Head Neck 2005; 27: 659-668
  • 130 Ravasco P, Monteiro-Grillo I, Vidal PM et al. Dietary counseling improves patient outcomes: a prospective, randomized, controlled trial in colorectal cancer patients undergoing radiotherapy. J Clin Oncol 2005; 23: 1431-1438
  • 131 van den Berg MG, Rasmussen-Conrad EL, Wei KH et al. Comparison of the effect of individual dietary counselling and of standard nutritional care on weight loss in patients with head and neck cancer undergoing radiotherapy. Br J Nutr 2010; 104: 872-877
  • 132 Ligthart-Melis GC, Weijs PJ, te Boveldt ND et al. Dietician-delivered intensive nutritional support is associated with a decrease in severe postoperative complications after surgery in patients with esophageal cancer. Dis Esophagus 2013; 26: 587-593
  • 133 Poulsen GM, Pedersen LL, Osterlind K et al. Randomized trial of the effects of individual nutritional counseling in cancer patients. Clin Nutr 2014; 33: 749-753
  • 134 Potter J, Langhorne P, Roberts M. Routine protein energy supplementation in adults: systematic review. BMJ 1998; 317: 495-501
  • 135 Ravasco P, Monteiro-Grillo I, Camilo M. Individualized nutrition intervention is of major benefit to colorectal cancer patients: long-term follow-up of a randomized controlled trial of nutritional therapy. Am J Clin Nutr 2012; 96: 1346-1353
  • 136 Baldwin C, Spiro A, McGough C et al. Simple nutritional intervention in patients with advanced cancers of the gastrointestinal tract, non-small cell lung cancers or mesothelioma and weight loss receiving chemotherapy: a randomised controlled trial. J Hum Nutr Diet 2011; 24: 431-440
  • 137 Baldwin C, Spiro A, Ahern R et al. Oral nutritional interventions in malnourished patients with cancer: a systematic review and meta-analysis. J Natl Cancer Inst 2012; 104: 371-385
  • 138 Balstad TR, Solheim TS, Strasser F et al. Dietary treatment of weight loss in patients with advanced cancer and cachexia: a systematic literature review. Crit Rev Oncol Hematol 2014; 91: 210-221
  • 139 Dy SM, Apostol CC. Evidence-based approaches to other symptoms in advanced cancer. Cancer J 2010; 16: 507-513
  • 140 Del Fabbro E, Hui D, Dalal S et al. Clinical outcomes and contributors to weight loss in a cancer cachexia clinic. J Palliat Med 2011; 14: 1004-1008
  • 141 Clutter Snyder D, Sloane R, Haines PS et al. The Diet Quality Index-Revised: a tool to promote and evaluate dietary change among older cancer survivors enrolled in a home-based intervention trial. J Am Diet Assoc 2007; 107: 1519-1529
  • 142 Bosaeus I. Nutritional support in multimodal therapy for cancer cachexia. Support Care Cancer 2008; 16: 447-451
  • 143 Hübner J, Marienfeld S, Abbenhardt C et al. Wie sinnvoll sind „Krebsdiäten“?. Deutsche medizinische Wochenschrift 2012; 137: 2417-2422
  • 144 Kasper H. Ernährungsmedizin und Diätetik. 10th. ed., München, Jena: Urban und Fischer; 2004
  • 145 Grossenbacher B, Hauser S. Ernährung und therapeutische Diäten bei Krebspatienten. 1th. ed., Bern: Huber Verlag; 1992
  • 146 Arends J. Gibt es eine Krebsdiät?. Forum 2011; 26: 25-29
  • 147 Allen BG, Bhatia SK, Anderson CM et al. Ketogenic diets as an adjuvant cancer therapy: History and potential mechanism. Redox Biol 2014; 2C: 963-970
  • 148 Bozzetti F, Zupec-Kania B. Toward a cancer-specific diet. Clin Nutr 2015; (im Druck) http://www.clinicalnutritionjournal.com/article/S0261-5614%2815%2900035-7/pdf
  • 149 Vidali S, Aminzadeh S, Lambert B et al. Mitochondria: The ketogenic diet-A metabolism-based therapy. Int J Biochem Cell Biol 2015; 63: 55-59
  • 150 Warburg O et al. Über den Stoffwechsel der Carzinomzelle. Biochem Zschr 1924; 152: 309-344
  • 151 Elstrom RL, Bauer DE, Buzzai M et al. Akt stimulates aerobic glycolysis in cancer cells. Cancer Res 2004; 64: 3892-3899
  • 152 Ho VW, Leung K, Hsu A et al. A low carbohydrate, high protein diet slows tumor growth and prevents cancer initiation. Cancer Res 2011; 71: 4484-4493
  • 153 Poff AM, Ari C, Seyfried TN et al. The ketogenic diet and hyperbaric oxygen therapy prolong survival in mice with systemic metastatic cancer. PLoS One 2013; 8: e65522
  • 154 Schmidt M, Pfetzer N, Schwab M et al. Effects of a ketogenic diet on the quality of life in 16 patients with advanced cancer: A pilot trial. Nutr Metab (Lond) 2011; 8: 54
  • 155 Arends J. Maligne Tumoren – Transketolase-like 1 (TKTL 1) – Ketogene Diät. Aktuel Ernahrungsmed 2008; 33: 80-81
  • 156 Bozzetti F, Cozzaglio L, Biganzoli E et al. Quality of life and length of survival in advanced cancer patients on home parenteral nutrition. Clin Nutr 2002; 21: 281-288
  • 157 Brennan MF, Ekman L. Metabolic consequences of nutritional support of the cancer patient. Cancer 1984; 54: 2627-2634
  • 158 Scolapio JS, Fleming CR, Kelly DG et al. Survival of home parenteral nutrition-treated patients: 20 years of experience at the Mayo Clinic. Mayo Clin Proc 1999; 74: 217-222
  • 159 Klein S, Koretz RL. Nutrition support in patients with cancer: what do the data really show?. Nutr Clin Pract 1994; 9: 91-100
  • 160 Koretz RL. Do data support nutrition support? Part II. enteral artificial nutrition. J Am Diet Assoc 2007; 107: 1374-1380
  • 161 Weimann A, Breitenstein S, Breuer JP et al. S3-Leitlinie der Deutschen Gesellschaft für Ernährungsmedizin (DGEM) in Zusammenarbeit mit der GESKES, der AKE, der DGCH, der DGAI und der DGAV: Klinische Ernährung in der Chirurgie. Aktuel Ernahrungsmed 2013; 38: 399-416
  • 162 Bischoff SC, Arends J, Dörje F et al. S3-Leitlinie der Deutschen Gesellschaft für Ernährungsmedizin (DGEM) in Zusammenarbeit mit der GESKES und der AKE. Künstliche Ernährung im ambulanten Bereich. Aktuel Ernahrungsmed 2013; 38: 101-154
  • 163 Nugent B, Lewis S, O’Sullivan JM. Enteral feeding methods for nutritional management in patients with head and neck cancers being treated with radiotherapy and/or chemotherapy. Cochrane Database Syst Rev 2010; 3 CD007904
  • 164 Burkitt P, Carter LM, Smith AB et al. Outcomes of percutaneous endoscopic gastrostomy and radiologically inserted gastrostomy in patients with head and neck cancer: a systematic review. Br J Oral Maxillofac Surg 2011; 49: 516-520
  • 165 Di Carlo I, Pulvirenti E, Mannino M et al. Increased use of percutaneous technique for totally implantable venous access devices. Is it real progress? A 27-year comprehensive review on early complications. Ann Surg Oncol 2010; 17: 1649-1656
  • 166 Rohrer S, Dietrich JW. Das Refeeding-Syndrom – Eine Literaturübersicht. Zeitschrift für Gastroenterologie 2014; 52: 593-600
  • 167 Walmsley RS. Refeeding syndrome: screening, incidence, and treatment during parenteral nutrition. J Gastroenterol Hepatol 2013; 28 (Suppl. 04) 113-117
  • 168 NICE. Nutrition support in adults. Oral nutrition support, enteral tube feeding and parenteral nutrition. NICE clinical guideline 2006; 32: 1-49
  • 169 Biolo G, Cederholm T, Muscaritoli M. Muscle contractile and metabolic dysfunction is a common feature of sarcopenia of aging and chronic diseases: from sarcopenic obesity to cachexia. Clin Nutr 2014; 33: 737-748
  • 170 English KL, Paddon-Jones D. Protecting muscle mass and function in older adults during bed rest. Curr Opin Clin Nutr Metab Care 2010; 13: 34-39
  • 171 Lira FS, Neto JC, Seelaender M. Exercise training as treatment in cancer cachexia. Appl Physiol Nutr Metab 2014; 39: 679-686
  • 172 Gould DW, Lahart I, Carmichael AR et al. Cancer cachexia prevention via physical exercise: molecular mechanisms. J Cachexia Sarcopenia Muscle 2013; 4: 111-124
  • 173 Scott JM, Khakoo A, Mackey JR et al. Modulation of anthracycline-induced cardiotoxicity by aerobic exercise in breast cancer: current evidence and underlying mechanisms. Circulation 2011; 124: 642-650
  • 174 Grande AJ, Silva V, Riera R et al. Exercise for cancer cachexia in adults. Cochrane Database Syst Rev 2014; 11 CD010804
  • 175 Dimeo FC, Stieglitz RD, Novelli-Fischer U et al. Effects of physical activity on the fatigue and psychologic status of cancer patients during chemotherapy. Cancer 1999; 85: 2273-2277
  • 176 Mock V, Pickett M, Ropka ME et al. Fatigue and quality of life outcomes of exercise during cancer treatment. Cancer Pract 2001; 9: 119-127
  • 177 Adamsen L, Midtgaard J, Rorth M et al. Feasibility, physical capacity, and health benefits of a multidimensional exercise program for cancer patients undergoing chemotherapy. Support Care Cancer 2003; 11: 707-716
  • 178 Halle M, Schoenberg MH. Physical activity in the prevention and treatment of colorectal carcinoma. Dtsch Arztebl Int 2009; 106: 722-727
  • 179 Oldervoll LM, Loge JH, Paltiel H et al. The effect of a physical exercise program in palliative care: A phase II study. J Pain Symptom Manage 2006; 31: 421-430
  • 180 Gulde I, Oldervoll LM, Martin C. Palliative cancer patients’ experience of physical activity. J Palliat Care 2011; 27: 296-302
  • 181 Oldervoll LM, Loge JH, Lydersen S et al. Physical exercise for cancer patients with advanced disease: a randomized controlled trial. Oncologist 2011; 16: 1649-1657
  • 182 Stene GB, Helbostad JL, Balstad TR et al. Effect of physical exercise on muscle mass and strength in cancer patients during treatment – a systematic review. Crit Rev Oncol Hematol 2013; 88: 573-593
  • 183 Cramp F, Byron-Daniel J. Exercise for the management of cancer-related fatigue in adults. Cochrane Database Syst Rev 2012; 11 CD006145
  • 184 Hoffman AJ, Brintnall RA, Brown JK et al. Too sick not to exercise: using a 6-week, home-based exercise intervention for cancer-related fatigue self-management for postsurgical non-small cell lung cancer patients. Cancer Nurs 2013; 36: 175-188
  • 185 Oldervoll LM, Loge JH, Paltiel H et al. Are palliative cancer patients willing and able to participate in a physical exercise program?. Palliat Support Care 2005; 3: 281-287
  • 186 Jones LW. Evidence-based risk assessment and recommendations for physical activity clearance: cancer. Appl Physiol Nutr Metab 2011; 36 (Suppl. 01) S101-S112
  • 187 Yavuzsen T, Davis MP, Walsh D et al. Systematic review of the treatment of cancer-associated anorexia and weight loss. J Clin Oncol 2005; 23: 8500-8511
  • 188 Paulsen O, Klepstad P, Rosland JH et al. Efficacy of methylprednisolone on pain, fatigue, and appetite loss in patients with advanced cancer using opioids: a randomized, placebo-controlled, double-blind trial. J Clin Oncol 2014; 32: 3221-3228
  • 189 Miller S, McNutt L, McCann MA et al. Use of corticosteroids for anorexia in palliative medicine: a systematic review. J Palliat Med 2014; 17: 482-485
  • 190 Ruiz Garcia V, Lopez-Briz E, Carbonell Sanchis R et al. Megestrol acetate for treatment of anorexia-cachexia syndrome. Cochrane Database Syst Rev 2013; 3 CD004310
  • 191 Strasser F, Luftner D, Possinger K et al. Cannabis-In-Cachexia-Study-Group. Comparison of orally administered cannabis extract and delta-9-tetrahydrocannabinol in treating patients with cancer-related anorexia-cachexia syndrome: a multicenter, phase III, randomized, double-blind, placebo-controlled clinical trial from the Cannabis-In-Cachexia-Study-Group. J Clin Oncol 2006; 24: 3394-3400
  • 192 Brisbois TD, de Kock IH, Watanabe SM et al. Delta-9-tetrahydrocannabinol may palliate altered chemosensory perception in cancer patients: results of a randomized, double-blind, placebo-controlled pilot trial. Ann Oncol 2011; 22: 2086-2093
  • 193 Jatoi A, Windschitl HE, Loprinzi CL et al. Dronabinol versus megestrol acetate versus combination therapy for cancer-associated anorexia: a North Central Cancer Treatment Group study. J Clin Oncol 2002; 20: 567-573
  • 194 Burney BO, Hayes TG, Smiechowska J et al. Low testosterone levels and increased inflammatory markers in patients with cancer and relationship with cachexia. J Clin Endocrinol Metab 2012; 97: E700-E709
  • 195 Chlebowski RT, Herrold J, Ali I et al. Influence of nandrolone decanoate on weight loss in advanced non-small cell lung cancer. Cancer 1986; 58: 183-186
  • 196 Loprinzi CL, Kugler JW, Sloan JA et al. Randomized comparison of megestrol acetate versus dexamethasone versus fluoxymesterone for the treatment of cancer anorexia/cachexia. J Clin Oncol 1999; 17: 3299-3306
  • 197 Lesser GJ, Case D, Ottery F et al. A phase III randomized study comparing the effects of oxandrolone (Ox) and megestrol acetate (Meg) on lean body mass (LBM), weight (wt) and quality of life (QOL) in patients with solid tumors and weight loss receiving chemotherapy. Journal of Clinical Oncology 2008; 26: 9513
  • 198 Dobs AS, Boccia RV, Croot CC et al. Effects of enobosarm on muscle wasting and physical function in patients with cancer: a double-blind, randomised controlled phase 2 trial. Lancet Oncol 2013; 14: 335-345
  • 199 Padhi D, Higano CS, Shore ND et al. Pharmacological inhibition of myostatin and changes in lean body mass and lower extremity muscle size in patients receiving androgen deprivation therapy for prostate cancer. J Clin Endocrinol Metab 2014; 99: E1967-E1975
  • 200 May PE, Barber A, D’Olimpio JT et al. Reversal of cancer-related wasting using oral supplementation with a combination of beta-hydroxy-beta-methylbutyrate, arginine, and glutamine. Am J Surg 2002; 183: 471-479
  • 201 Clark RH, Feleke G, Din M et al. Nutritional treatment for acquired immunodeficiency virus-associated wasting using beta-hydroxy beta-methylbutyrate, glutamine, and arginine: a randomized, double-blind, placebo-controlled study. JPEN J Parenter Enteral Nutr 2000; 24: 133-139
  • 202 Berk L, James J, Schwartz A et al. A randomized, double-blind, placebo-controlled trial of a beta-hydroxyl beta-methyl butyrate, glutamine, and arginine mixture for the treatment of cancer cachexia (RTOG 0122). Support Care Cancer 2008; 16: 1179-1188
  • 203 Deutz NE, Safar A, Schutzler S et al. Muscle protein synthesis in cancer patients can be stimulated with a specially formulated medical food. Clin Nutr 2011; 30: 759-768
  • 204 Tayek JA, Bistrian BR, Hehir DJ et al. Improved protein kinetics and albumin synthesis by branched chain amino acid-enriched total parenteral nutrition in cancer cachexia. A prospective randomized crossover trial. Cancer 1986; 58: 147-157
  • 205 Poon RT, Yu WC, Fan ST et al. Long-term oral branched chain amino acids in patients undergoing chemoembolization for hepatocellular carcinoma: a randomized trial. Aliment Pharmacol Ther 2004; 19: 779-788
  • 206 van Loon LJ. Leucine as a pharmaconutrient in health and disease. Curr Opin Clin Nutr Metab Care 2012; 15: 71-77
  • 207 Ham DJ, Caldow MK, Lynch GS et al. Leucine as a treatment for muscle wasting: a critical review. Clin Nutr 2014; 33: 937-945
  • 208 Pearlstone DB, Wolf RF, Berman RS et al. Effect of systemic insulin on protein kinetics in postoperative cancer patients. Ann Surg Oncol 1994; 1: 321-332
  • 209 Fouladiun M, Korner U, Bosaeus I et al. Body composition and time course changes in regional distribution of fat and lean tissue in unselected cancer patients on palliative care – correlations with food intake, metabolism, exercise capacity, and hormones. Cancer 2005; 103: 2189-2198
  • 210 Murphy RA, Wilke MS, Perrine M et al. Loss of adipose tissue and plasma phospholipids: relationship to survival in advanced cancer patients. Clin Nutr 2010; 29: 482-487
  • 211 Lundholm K, Korner U, Gunnebo L et al. Insulin treatment in cancer cachexia: effects on survival, metabolism, and physical functioning. Clin Cancer Res 2007; 13: 2699-2706
  • 212 Velloso CP. Regulation of muscle mass by growth hormone and IGF-I. Br J Pharmacol 2008; 154: 557-568
  • 213 Boyd DB. Insulin and cancer. Integr Cancer Ther 2003; 2: 315-329
  • 214 Salisbury TB, Tomblin JK. Insulin/Insulin-like growth factors in cancer: new roles for the aryl hydrocarbon receptor, tumor resistance mechanisms, and new blocking strategies. Front Endocrinol (Lausanne) 2015; 6: 12
  • 215 Baserga R. The insulin-like growth factor-I receptor as a target for cancer therapy. Expert Opin Ther Targets 2005; 9: 753-768
  • 216 Colmers IN, Bowker SL, Tjosvold LA et al. Insulin use and cancer risk in patients with type 2 diabetes: a systematic review and meta-analysis of observational studies. Diabetes Metab 2012; 38: 485-506
  • 217 Jenkins PJ, Mukherjee A, Shalet SM. Does growth hormone cause cancer?. Clin Endocrinol (Oxf) 2006; 64: 115-121
  • 218 Strasser F, Lutz TA, Maeder MT et al. Safety, tolerability and pharmacokinetics of intravenous ghrelin for cancer-related anorexia/cachexia: a randomised, placebo-controlled, double-blind, double-crossover study. Br J Cancer 2008; 98: 300-308
  • 219 Temel J, Currow D, Fearon K et al. Anamorelin for the treatment of cancer anorexia-cachexia in NSCLC: results from the phase 3 studies Romana 1 and 2. Ann Oncol 2014; 25: v1-v41
  • 220 Solheim TS, Fearon KC, Blum D et al. Non-steroidal anti-inflammatory treatment in cancer cachexia: a systematic literature review. Acta Oncol 2013; 52: 6-17
  • 221 Lundholm K, Gelin J, Hyltander A et al. Anti-inflammatory treatment may prolong survival in undernourished patients with metastatic solid tumors. Cancer Res 1994; 54: 5602-5606
  • 222 Lundholm K, Daneryd P, Korner U et al. Evidence that long-term COX-treatment improves energy homeostasis and body composition in cancer patients with progressive cachexia. Int J Oncol 2004; 24: 505-512
  • 223 Arzneimittelkommission der deutschen Ärzteschaft. Nichtsteroidale Antirheumatika (NSAR) im Vergleich: Risiko von Komplikationen im oberen Gastrointestinaltrakt, Herzinfarkt und Schlaganfall. Deutsches Ärzteblatt 2013; 110: A1447-A1448
  • 224 van der Meij BS, Langius JA, Smit EF et al. Oral nutritional supplements containing (n-3) polyunsaturated fatty acids affect the nutritional status of patients with stage III non-small cell lung cancer during multimodality treatment. J Nutr 2010; 140: 1774-1780
  • 225 de Aguiar Pastore Silva J, de Moraes Trindade EB, de Souza Fabre ME et al. Fish oil supplement alters markers of inflammatory and nutritional status in colorectal cancer patients. Nutr Cancer 2012; 64: 267-273
  • 226 Mocellin MC, de Aguiar Pastore Silva J, de Quadros Camargo C et al. Fish oil decreases C-reactive protein/albumin ratio improving nutritional prognosis and plasma fatty acid profile in colorectal cancer patients. Lipids 2013; 48: 879-888
  • 227 Murphy RA, Mourtzakis M, Chu QS et al. Nutritional intervention with fish oil provides a benefit over standard of care for weight and skeletal muscle mass in patients with nonsmall cell lung cancer receiving chemotherapy. Cancer 2011; 117: 1775-1782
  • 228 Trabal J, Leyes P, Forga M et al. Potential usefulness of an EPA-enriched nutritional supplement on chemotherapy tolerability in cancer patients without overt malnutrition. Nutr Hosp 2010; 25: 736-740
  • 229 Sanchez-Lara K, Turcott JG, Juarez-Hernandez E et al. Effects of an oral nutritional supplement containing eicosapentaenoic acid on nutritional and clinical outcomes in patients with advanced non-small cell lung cancer: randomised trial. Clin Nutr 2014; 33: 1017-1023
  • 230 Murphy RA, Mourtzakis M, Chu QS et al. Supplementation with fish oil increases first-line chemotherapy efficacy in patients with advanced nonsmall cell lung cancer. Cancer 2011; 117: 3774-3780
  • 231 Gogos CA, Ginopoulos P, Salsa B et al. Dietary omega-3 polyunsaturated fatty acids plus vitamin E restore immunodeficiency and prolong survival for severely ill patients with generalized malignancy: a randomized control trial. Cancer 1998; 82: 395-402
  • 232 de Aguiar Pastore Silva J, Emilia de Souza Fabre M, Waitzberg DL. Omega-3 supplements for patients in chemotherapy and/or radiotherapy: A systematic review. Clin Nutr 2015; 34: 359-366
  • 233 van der Meij BS, Langius JA, Spreeuwenberg MD et al. Oral nutritional supplements containing n-3 polyunsaturated fatty acids affect quality of life and functional status in lung cancer patients during multimodality treatment: an RCT. Eur J Clin Nutr 2012; 66: 399-404
  • 234 Fearon KC, Barber MD, Moses AG et al. Double-blind, placebo-controlled, randomized study of eicosapentaenoic acid diester in patients with cancer cachexia. J Clin Oncol 2006; 24: 3401-3407
  • 235 Fearon KC, Von Meyenfeldt MF, Moses AG et al. Effect of a protein and energy dense N-3 fatty acid enriched oral supplement on loss of weight and lean tissue in cancer cachexia: a randomised double blind trial. Gut 2003; 52: 1479-1486
  • 236 Jatoi A, Rowland K, Loprinzi CL et al. An eicosapentaenoic acid supplement versus megestrol acetate versus both for patients with cancer-associated wasting: a North Central Cancer Treatment Group and National Cancer Institute of Canada collaborative effort. J Clin Oncol 2004; 22: 2469-2476
  • 237 Dewey A, Baughan C, Dean T et al. Eicosapentaenoic acid (EPA, an omega-3 fatty acid from fish oils) for the treatment of cancer cachexia. Cochrane Database Syst Rev 2007; 1 CD004597
  • 238 Ries A, Trottenberg P, Elsner F et al. A systematic review on the role of fish oil for the treatment of cachexia in advanced cancer: an EPCRC cachexia guidelines project. Palliat Med 2012; 26: 294-304
  • 239 Colomer R, Moreno-Nogueira JM, Garcia-Luna PP et al. N-3 fatty acids, cancer and cachexia: a systematic review of the literature. Br J Nutr 2007; 97: 823-831
  • 240 Bruera E, Strasser F, Palmer JL et al. Effect of fish oil on appetite and other symptoms in patients with advanced cancer and anorexia/cachexia: a double-blind, placebo-controlled study. J Clin Oncol 2003; 21: 129-134
  • 241 Kuhn KS, Muscaritoli M, Wischmeyer P et al. Glutamine as indispensable nutrient in oncology: experimental and clinical evidence. Eur J Nutr 2010; 49: 197-210
  • 242 Alpers DH. Glutamine: do the data support the cause for glutamine supplementation in humans?. Gastroenterology 2006; 130: S106-S116
  • 243 DeBerardinis RJ, Mancuso A, Daikhin E et al. Beyond aerobic glycolysis: transformed cells can engage in glutamine metabolism that exceeds the requirement for protein and nucleotide synthesis. Proc Natl Acad Sci U S A 2007; 104: 19345-19350
  • 244 Huang W, Choi W, Chen Y et al. A proposed role for glutamine in cancer cell growth through acid resistance. Cell Res 2013; 23: 724-727
  • 245 Wischmeyer PE, Dhaliwal R, McCall M et al. Parenteral glutamine supplementation in critical illness: a systematic review. Crit Care 2014; 18: R76
  • 246 Heyland D, Muscedere J, Wischmeyer PE et al. A randomized trial of glutamine and antioxidants in critically ill patients. N Engl J Med 2013; 368: 1489-1497
  • 247 Holecek M. Side effects of long-term glutamine supplementation. JPEN J Parenter Enteral Nutr 2013; 37: 607-616
  • 248 Lyckholm L, Heddinger SP, Parker G et al. A randomized, placebo controlled trial of oral zinc for chemotherapy-related taste and smell disorders. J Pain Palliat Care Pharmacother 2012; 26: 111-114
  • 249 Kardinal CG, Loprinzi CL, Schaid DJ et al. A controlled trial of cyproheptadine in cancer patients with anorexia and/or cachexia. Cancer 1990; 65: 2657-2662
  • 250 Lundholm K, Gunnebo L, Korner U et al. Effects by daily long term provision of ghrelin to unselected weight-losing cancer patients: a randomized double-blind study. Cancer 2010; 116: 2044-2052
  • 251 Adachi S, Takiguchi S, Okada K et al. Effects of ghrelin administration after total gastrectomy: a prospective, randomized, placebo-controlled phase II study. Gastroenterology 2010; 138: 1312-1320
  • 252 Garcia JM, Friend J, Allen S. Therapeutic potential of anamorelin, a novel, oral ghrelin mimetic, in patients with cancer-related cachexia: a multicenter, randomized, double-blind, crossover, pilot study. Support Care Cancer 2013; 21: 129-137
  • 253 Ando K, Takahashi F, Kato M et al. Tocilizumab, a proposed therapy for the cachexia of Interleukin6-expressing lung cancer. PLoS One 2014; 9: e102436
  • 254 Hirata H, Tetsumoto S, Kijima T et al. Favorable responses to tocilizumab in two patients with cancer-related cachexia. J Pain Symptom Manage 2013; 46: e9-e13
  • 255 Verstovsek S, Kantarjian H, Mesa RA et al. Safety and efficacy of INCB018424, a JAK1 and JAK2 inhibitor, in myelofibrosis. N Engl J Med 2010; 363: 1117-1127
  • 256 Wilkes EA, Selby AL, Cole AT et al. Poor tolerability of thalidomide in end-stage oesophageal cancer. Eur J Cancer Care (Engl) 2011; 20: 593-600
  • 257 Yennurajalingam S, Willey JS, Palmer JL et al. The role of thalidomide and placebo for the treatment of cancer-related anorexia-cachexia symptoms: results of a double-blind placebo-controlled randomized study. J Palliat Med 2012; 15: 1059-1064
  • 258 Reid J, Mills M, Cantwell M et al. Thalidomide for managing cancer cachexia. Cochrane Database Syst Rev 2012; 4 CD008664
  • 259 McMillan DC. Systemic inflammation, nutritional status and survival in patients with cancer. Curr Opin Clin Nutr Metab Care 2009; 12: 223-226
  • 260 Del Fabbro E, Dev R, Hui D et al. Effects of melatonin on appetite and other symptoms in patients with advanced cancer and cachexia: a double-blind placebo-controlled trial. J Clin Oncol 2013; 31: 1271-1276
  • 261 Lissoni P, Paolorossi F, Tancini G et al. Is there a role for melatonin in the treatment of neoplastic cachexia?. Eur J Cancer 1996; 32A: 1340-1343
  • 262 Mills E, Wu P, Seely D et al. Melatonin in the treatment of cancer: a systematic review of randomized controlled trials and meta-analysis. J Pineal Res 2005; 39: 360-366
  • 263 Jatoi A, Alberts SR, Foster N et al. Is bortezomib, a proteasome inhibitor, effective in treating cancer-associated weight loss? Preliminary results from the North Central Cancer Treatment Group. Support Care Cancer 2005; 13: 381-386
  • 264 Beijer S, Hupperets PS, van den Borne BE et al. Effect of adenosine 5’-triphosphate infusions on the nutritional status and survival of preterminal cancer patients. Anticancer Drugs 2009; 20: 625-633
  • 265 Beijer S, Hupperets PS, van den Borne BE et al. Randomized clinical trial on the effects of adenosine 5’-triphosphate infusions on quality of life, functional status, and fatigue in preterminal cancer patients. J Pain Symptom Manage 2010; 40: 520-530
  • 266 Carbo N, Lopez-Soriano J, Costelli P et al. Interleukin-15 antagonizes muscle protein waste in tumour-bearing rats. Br J Cancer 2000; 83: 526-531
  • 267 Kraft M, Kraft K, Gartner S et al. L-Carnitine-supplementation in advanced pancreatic cancer (CARPAN) – a randomized multicentre trial. Nutr J 2012; 11: 52
  • 268 Prado CM, Bekaii-Saab T, Doyle LA et al. Skeletal muscle anabolism is a side effect of therapy with the MEK inhibitor: selumetinib in patients with cholangiocarcinoma. Br J Cancer 2012; 106: 1583-1586
  • 269 Thiel HJ, Fietkau R, Sauer R. Malnutrition and the role of nutritional support for radiation therapy patients. Recent Results Cancer Res 1988; 108: 205-226
  • 270 Nayel H, el-Ghoneimy E, el-Haddad S. Impact of nutritional supplementation on treatment delay and morbidity in patients with head and neck tumors treated with irradiation. Nutrition 1992; 8: 13-18
  • 271 Paccagnella A, Morello M, Da Mosto MC et al. Early nutritional intervention improves treatment tolerance and outcomes in head and neck cancer patients undergoing concurrent chemoradiotherapy. Support Care Cancer 2010; 18: 837-845
  • 272 Nugent B, Lewis S, O’Sullivan JM. Enteral feeding methods for nutritional management in patients with head and neck cancers being treated with radiotherapy and/or chemotherapy. Cochrane Database Syst Rev 2013; 1 CD007904
  • 273 Fietkau R, Iro H, Sailer D et al. Percutaneous endoscopically guided gastrostomy in patients with head and neck cancer. Recent Results Cancer Res 1991; 121: 269-282
  • 274 Tyldesley S, Sheehan F, Munk P et al. The use of radiologically placed gastrostomy tubes in head and neck cancer patients receiving radiotherapy. Int J Radiat Oncol Biol Phys 1996; 36: 1205-1209
  • 275 Bozzetti F, Cozzaglio L, Gavazzi C et al. Nutritional support in patients with cancer of the esophagus: impact on nutritional status, patient compliance to therapy, and survival. Tumori 1998; 84: 681-686
  • 276 Lee JH, Machtay M, Unger LD et al. Prophylactic gastrostomy tubes in patients undergoing intensive irradiation for cancer of the head and neck. Arch Otolaryngol Head Neck Surg 1998; 124: 871-875
  • 277 van den Berg MG, Rasmussen-Conrad EL, van Nispen L et al. A prospective study on malnutrition and quality of life in patients with head and neck cancer. Oral Oncol 2008; 44: 830-837
  • 278 Elia M, Van Bokhorst-de van der Schueren MA, Garvey J et al. Enteral (oral or tube administration) nutritional support and eicosapentaenoic acid in patients with cancer: a systematic review. Int J Oncol 2006; 28: 5-23
  • 279 Isenring EA, Bauer JD, Capra S. Nutrition support using the American Dietetic Association medical nutrition therapy protocol for radiation oncology patients improves dietary intake compared with standard practice. J Am Diet Assoc 2007; 107: 404-412
  • 280 Fietkau R. Principles of feeding cancer patients via enteral or parenteral nutrition during radiotherapy. Strahlenther Onkol 1998; 174 (Suppl. 03) 47-51
  • 281 Cereda E, Cappello S, Caccialanza R. The use of oral nutritional supplements in patients with head and neck cancer receiving (chemo)radiotherapy. Clin Nutr 2014; 33: 370
  • 282 Langius JA, Zandbergen MC, Eerenstein SE et al. Effect of nutritional interventions on nutritional status, quality of life and mortality in patients with head and neck cancer receiving (chemo)radiotherapy: a systematic review. Clin Nutr 2013; 32: 671-678
  • 283 Head and Neck Guideline Steering Committee. Evidence-based practice guidelines for the nutritional management of adult patients with head and neck cancer. Sydney: Cancer Council Australia; Version URL: http://wiki.cancer.org.au/australiawiki/index.php?oldid=76062 (cited 2015 Jun 17)
  • 284 Isenring E et al. Updated evidence-based practice guidelines for the nutritional management of patients receiving radiation therapy and/or chemotherapy.  Nutrition Dietetics 2013; 70: 312-324
  • 285 Marcy PY, Magne N, Bensadoun RJ et al. Systematic percutaneous fluoroscopic gastrostomy for concomitant radiochemotherapy of advanced head and neck cancer: optimization of therapy. Support Care Cancer 2000; 8: 410-413
  • 286 Rabinovitch R, Grant B, Berkey BA et al. Impact of nutrition support on treatment outcome in patients with locally advanced head and neck squamous cell cancer treated with definitive radiotherapy: a secondary analysis of RTOG trial 90-03. Head Neck 2006; 28: 287-296
  • 287 Campos AC, Butters M, Meguid MM. Home enteral nutrition via gastrostomy in advanced head and neck cancer patients. Head Neck 1990; 12: 137-142
  • 288 Fietkau R, Lewitzki V, Kuhnt T et al. A disease-specific enteral nutrition formula improves nutritional status and functional performance in patients with head and neck and esophageal cancer undergoing chemoradiotherapy: results of a randomized, controlled, multicenter trial. Cancer 2013; 119: 3343-3353
  • 289 Lewis SL, Brody R, Touger-Decker R et al. Feeding tube use in patients with head and neck cancer. Head Neck 2014; 36: 1789-1795
  • 290 Trotti A, Bellm LA, Epstein JB et al. Mucositis incidence, severity and associated outcomes in patients with head and neck cancer receiving radiotherapy with or without chemotherapy: a systematic literature review. Radiother Oncol 2003; 66: 253-262
  • 291 Campos MI, Campos CN, Aarestrup FM et al. Oral mucositis in cancer treatment: Natural history, prevention and treatment. Mol Clin Oncol 2014; 2: 337-340
  • 292 Mekhail TM, Adelstein DJ, Rybicki LA et al. Enteral nutrition during the treatment of head and neck carcinoma: is a percutaneous endoscopic gastrostomy tube preferable to a nasogastric tube?. Cancer 2001; 91: 1785-1790
  • 293 Daly JM, Hearne B, Dunaj J et al. Nutritional rehabilitation in patients with advanced head and neck cancer receiving radiation therapy. Am J Surg 1984; 148: 514-520
  • 294 Cannaby AM, Evans L, Freeman A. Nursing care of patients with nasogastric feeding tubes. Br J Nurs 2002; 11: 366-372
  • 295 Corry J, Poon W, McPhee N et al. Randomized study of percutaneous endoscopic gastrostomy versus nasogastric tubes for enteral feeding in head and neck cancer patients treated with (chemo)radiation. J Med Imaging Radiat Oncol 2008; 52: 503-510
  • 296 Lees J. Nasogastric and percutaneous endoscopic gastrostomy feeding in head and neck cancer patients receiving radiotherapy treatment at a regional oncology unit: a two year study. Eur J Cancer Care (Engl) 1997; 6: 45-49
  • 297 Gomes Jr CA, Lustosa SA, Matos D et al. Percutaneous endoscopic gastrostomy versus nasogastric tube feeding for adults with swallowing disturbances. Cochrane Database Syst Rev 2012; 3 CD008096
  • 298 Paleri V, Patterson J. Use of gastrostomy in head and neck cancer: a systematic review to identify areas for future research. Clin Otolaryngol 2010; 35: 177-189
  • 299 Wang J, Liu M, Liu C et al. Percutaneous endoscopic gastrostomy versus nasogastric tube feeding for patients with head and neck cancer: a systematic review. J Radiat Res 2014; 55: 559-567
  • 300 Savarese DM, Savy G, Vahdat L et al. Prevention of chemotherapy and radiation toxicity with glutamine. Cancer Treat Rev 2003; 29: 501-513
  • 301 Huang EY, Leung SW, Wang CJ et al. Oral glutamine to alleviate radiation-induced oral mucositis: a pilot randomized trial. Int J Radiat Oncol Biol Phys 2000; 46: 535-539
  • 302 Cerchietti LC, Navigante AH, Lutteral MA et al. Double-blinded, placebo-controlled trial on intravenous L-alanyl-L-glutamine in the incidence of oral mucositis following chemoradiotherapy in patients with head-and-neck cancer. Int J Radiat Oncol Biol Phys 2006; 65: 1330-1337
  • 303 Topkan E, Parlak C, Topuk S et al. Influence of oral glutamine supplementation on survival outcomes of patients treated with concurrent chemoradiotherapy for locally advanced non-small cell lung cancer. BMC Cancer 2012; 12: 502
  • 304 Kozelsky TF, Meyers GE, Sloan JA et al. Phase III double-blind study of glutamine versus placebo for the prevention of acute diarrhea in patients receiving pelvic radiation therapy. J Clin Oncol 2003; 21: 1669-1674
  • 305 Rotovnik Kozjek N, Kompan L, Soeters P et al. Oral glutamine supplementation during preoperative radiochemotherapy in patients with rectal cancer: a randomised double blinded, placebo controlled pilot study. Clin Nutr 2011; 30: 567-570
  • 306 Vidal-Casariego A, Calleja-Fernandez A, de Urbina-Gonzalez JJ et al. Efficacy of glutamine in the prevention of acute radiation enteritis: a randomized controlled trial. JPEN J Parenter Enteral Nutr 2014; 38: 205-213
  • 307 Kucuktulu E, Guner A, Kahraman I et al. The protective effects of glutamine on radiation-induced diarrhea. Support Care Cancer 2013; 21: 1071-1075
  • 308 Rubio I, Suva LJ, Todorova V et al. Oral glutamine reduces radiation morbidity in breast conservation surgery. JPEN J Parenter Enteral Nutr 2013; 37: 623-630
  • 309 Eda K, Uzer K, Murat T et al. The effects of enteral glutamine on radiotherapy induced dermatitis in breast cancer. Clin Nutr 2015; Mar 26. pii: S0261-5614(15)00084-9. DOI: 10.1016/j.clnu.2015.03.009. [Epub ahead of print]
  • 310 Khalid U, McGough C, Hackett C et al. A modified inflammatory bowel disease questionnaire and the Vaizey Incontinence questionnaire are more sensitive measures of acute gastrointestinal toxicity during pelvic radiotherapy than RTOG grading. Int J Radiat Oncol Biol Phys 2006; 64: 1432-1441
  • 311 Andreyev HJ, Wotherspoon A, Denham JW et al. “Pelvic radiation disease”: new understanding and new solutions for a new disease in the era of cancer survivorship. Scand J Gastroenterol 2011; 46: 389-397
  • 312 Andreyev J. Gastrointestinal symptoms after pelvic radiotherapy: a new understanding to improve management of symptomatic patients. Lancet Oncol 2007; 8: 1007-1017
  • 313 Demers M, Dagnault A, Desjardins J. A randomized double-blind controlled trial: impact of probiotics on diarrhea in patients treated with pelvic radiation. Clin Nutr 2014; 33: 761-767
  • 314 Salminen E, Elomaa I, Minkkinen J et al. Preservation of intestinal integrity during radiotherapy using live Lactobacillus acidophilus cultures. Clin Radiol 1988; 39: 435-437
  • 315 Urbancsek H, Kazar T, Mezes I et al. Results of a double-blind, randomized study to evaluate the efficacy and safety of Antibiophilus in patients with radiation-induced diarrhoea. Eur J Gastroenterol Hepatol 2001; 13: 391-396
  • 316 Delia P, Sansotta G, Donato V et al. Use of probiotics for prevention of radiation-induced diarrhea. World J Gastroenterol 2007; 13: 912-915
  • 317 Giralt J, Regadera JP, Verges R et al. Effects of probiotic Lactobacillus casei DN-114 001 in prevention of radiation-induced diarrhea: results from multicenter, randomized, placebo-controlled nutritional trial. Int J Radiat Oncol Biol Phys 2008; 71: 1213-1219
  • 318 Chitapanarux I, Chitapanarux T, Traisathit P et al. Randomized controlled trial of live lactobacillus acidophilus plus bifidobacterium bifidum in prophylaxis of diarrhea during radiotherapy in cervical cancer patients. Radiat Oncol 2010; 5: 31
  • 319 Wedlake LJ, Shaw C, Whelan K et al. Systematic review: the efficacy of nutritional interventions to counteract acute gastrointestinal toxicity during therapeutic pelvic radiotherapy. Aliment Pharmacol Ther 2013; 37: 1046-1056
  • 320 Gibson RJ, Keefe DM, Lalla RV et al. Systematic review of agents for the management of gastrointestinal mucositis in cancer patients. Support Care Cancer 2013; 21: 313-326
  • 321 Hamad A, Fragkos KC, Forbes A. A systematic review and meta-analysis of probiotics for the management of radiation induced bowel disease. Clin Nutr 2013; 32: 353-360
  • 322 Miyata H, Yano M, Yasuda T et al. Randomized study of clinical effect of enteral nutrition support during neoadjuvant chemotherapy on chemotherapy-related toxicity in patients with esophageal cancer. Clin Nutr 2012; 31: 330-336
  • 323 Conklin KA. Dietary antioxidants during cancer chemotherapy: impact on chemotherapeutic effectiveness and development of side effects. Nutr Cancer 2000; 37: 1-18
  • 324 Conklin KA. Cancer chemotherapy and antioxidants. J Nutr 2004; 134: 3201S-3204S
  • 325 Watson J. Oxidants, antioxidants and the current incurability of metastatic cancers. Open Biol 2013; 3: 120144
  • 326 Chen Q, Espey MG, Krishna MC et al. Pharmacologic ascorbic acid concentrations selectively kill cancer cells: action as a pro-drug to deliver hydrogen peroxide to tissues. Proc Natl Acad Sci U S A 2005; 102: 13604-13609
  • 327 Heaney ML, Gardner JR, Karasavvas N et al. Vitamin C antagonizes the cytotoxic effects of antineoplastic drugs. Cancer Res 2008; 68: 8031-8038
  • 328 Zou W, Yue P, Lin N et al. Vitamin C inactivates the proteasome inhibitor PS-341 in human cancer cells. Clin Cancer Res 2006; 12: 273-280
  • 329 Perrone G, Hideshima T, Ikeda H et al. Ascorbic acid inhibits antitumor activity of bortezomib in vivo. Leukemia 2009; 23: 1679-1686
  • 330 Golden EB, Lam PY, Kardosh A et al. Green tea polyphenols block the anticancer effects of bortezomib and other boronic acid-based proteasome inhibitors. Blood 2009; 113: 5927-5937
  • 331 Hoffer LJ, Levine M, Assouline S et al. Phase I clinical trial of i.v. ascorbic acid in advanced malignancy. Ann Oncol 2008; 19: 1969-1974
  • 332 Pace A, Savarese A, Picardo M et al. Neuroprotective effect of vitamin E supplementation in patients treated with cisplatin chemotherapy. J Clin Oncol 2003; 21: 927-931
  • 333 Cascinu S, Catalano V, Cordella L et al. Neuroprotective effect of reduced glutathione on oxaliplatin-based chemotherapy in advanced colorectal cancer: a randomized, double-blind, placebo-controlled trial. J Clin Oncol 2002; 20: 3478-3483
  • 334 Ng K, Meyerhardt JA, Chan JA et al. Multivitamin use is not associated with cancer recurrence or survival in patients with stage III colon cancer: findings from CALGB 89803. J Clin Oncol 2010; 28: 4354-4363
  • 335 Dennert G, Horneber M. Selenium for alleviating the side effects of chemotherapy, radiotherapy and surgery in cancer patients. Cochrane Database Syst Rev 2006; 3 CD005037
  • 336 Li Y, Ping X, Yu B et al. Clinical trial: prophylactic intravenous alanyl-glutamine reduces the severity of gastrointestinal toxicity induced by chemotherapy – a randomized crossover study. Aliment Pharmacol Ther 2009; 30: 452-458
  • 337 Sun J, Wang H, Hu H. Glutamine for chemotherapy induced diarrhea: a meta-analysis. Asia Pac J Clin Nutr 2012; 21: 380-385
  • 338 Sornsuvit C, Komindr S, Chuncharunee S et al. Pilot Study: effects of parenteral glutamine dipeptide supplementation on neutrophil functions and prevention of chemotherapy-induced side-effects in acute myeloid leukaemia patients. J Int Med Res 2008; 36: 1383-1391
  • 339 Wang WS, Lin JK, Lin TC et al. Oral glutamine is effective for preventing oxaliplatin-induced neuropathy in colorectal cancer patients. Oncologist 2007; 12: 312-319
  • 340 Daenen L, Cirkel G, Houthuijzen J et al. Increased Plasma Levels of Chemoresistance-Inducing Fatty Acid 16:4(n-3) After Consumption of Fish and Fish Oil. JAMA Oncol 2015; DOI: 10.1001/jamaoncol.2015.0388. (Published online April 02)
  • 341 Roodhart JM, Daenen LG, Stigter EC et al. Mesenchymal stem cells induce resistance to chemotherapy through the release of platinum-induced fatty acids. Cancer Cell 2011; 20: 370-383
  • 342 Murphy RA, Clandinin MT, Chu QS et al. A fishy conclusion regarding n-3 fatty acid supplementation in cancer patients. Clin Nutr 2013; 32: 466-467
  • 343 Pardini RS. Nutritional intervention with omega-3 fatty acids enhances tumor response to anti-neoplastic agents. Chem Biol Interact 2006; 162: 89-105
  • 344 Hardman WE. (N-3) Fatty Acids and Cancer Therapy. J Nutr 2004; 134: 3427S-3430S
  • 345 Serafini P. Editorial: PGE2-producing MDSC: a role in tumor progression?. J Leukoc Biol 2010; 88: 827-829
  • 346 Bougnoux P, Hajjaji N, Ferrasson MN et al. Improving outcome of chemotherapy of metastatic breast cancer by docosahexaenoic acid: a phase II trial. Br J Cancer 2009; 101: 1978-1985
  • 347 Michael-Titus AT, Priestley JV. Omega-3 fatty acids and traumatic neurological injury: from neuroprotection to neuroplasticity?. Trends Neurosci 2014; 37: 30-38
  • 348 Coste TC, Gerbi A, Vague P et al. Neuroprotective effect of docosahexaenoic acid-enriched phospholipids in experimental diabetic neuropathy. Diabetes 2003; 52: 2578-2585
  • 349 Ghoreishi Z, Esfahani A, Djazayeri A et al. Omega-3 fatty acids are protective against paclitaxel-induced peripheral neuropathy: a randomized double-blind placebo controlled trial. BMC Cancer 2012; 12: 355
  • 350 Seguy D, Duhamel A, Rejeb MB et al. Better outcome of patients undergoing enteral tube feeding after myeloablative conditioning for allogeneic stem cell transplantation. Transplantation 2012; 94: 287-294
  • 351 Sheean PM, Braunschweig CA. Exploring the clinical characteristics of parenteral nutrition recipients admitted for initial hematopoietic stem cell transplantation. J Am Diet Assoc 2007; 107: 1398-1403
  • 352 Uderzo C, Rebora P, Marrocco E et al. Glutamine-enriched nutrition does not reduce mucosal morbidity or complications after stem-cell transplantation for childhood malignancies: a prospective randomized study. Transplantation 2011; 91: 1321-1325
  • 353 Blijlevens NM, Donnelly JP, Naber AH et al. A randomised, double-blinded, placebo-controlled, pilot study of parenteral glutamine for allogeneic stem cell transplant patients. Support Care Cancer 2005; 13: 790-796
  • 354 Calle EE, Rodriguez C, Walker-Thurmond K et al. Overweight, obesity, and mortality from cancer in a prospectively studied cohort of U.S. adults. N Engl J Med 2003; 348: 1625-1638
  • 355 Hu J, La Vecchia C, Augustin LS et al. Glycemic index, glycemic load and cancer risk. Ann Oncol 2013; 24: 245-251
  • 356 Meyerhardt JA, Sato K, Niedzwiecki D et al. Dietary glycemic load and cancer recurrence and survival in patients with stage III colon cancer: findings from CALGB 89803. J Natl Cancer Inst 2012; 104: 1702-1711
  • 357 Patel AV, Feigelson HS, Talbot JT et al. The role of body weight in the relationship between physical activity and endometrial cancer: results from a large cohort of US women. Int J Cancer 2008; 123: 1877-1882
  • 358 Holmes MD, Chen WY, Feskanich D et al. Physical activity and survival after breast cancer diagnosis. JAMA 2005; 293: 2479-2486
  • 359 Meyerhardt JA, Giovannucci EL, Holmes MD et al. Physical activity and survival after colorectal cancer diagnosis. J Clin Oncol 2006; 24: 3527-3534
  • 360 Meyerhardt JA, Heseltine D, Niedzwiecki D et al. Impact of physical activity on cancer recurrence and survival in patients with stage III colon cancer: findings from CALGB 89803. J Clin Oncol 2006; 24: 3535-3541
  • 361 Guinan E, Hussey J, Broderick JM et al. The effect of aerobic exercise on metabolic and inflammatory markers in breast cancer survivors – a pilot study. Support Care Cancer 2013; 21: 1983-1992
  • 362 Anderson AS, Craigie AM, Caswell S et al. The impact of a bodyweight and physical activity intervention (BeWEL) initiated through a national colorectal cancer screening programme: randomised controlled trial. BMJ 2014; 348: g1823
  • 363 Gibson TM, Park Y, Robien K et al. Body mass index and risk of second obesity-associated cancers after colorectal cancer: a pooled analysis of prospective cohort studies. J Clin Oncol 2014; 32: 4004-4011
  • 364 Ainsworth BE, Haskell WL, Whitt MC et al. Compendium of physical activities: an update of activity codes and MET intensities. Med Sci Sports Exerc 2000; 32: S498-S504
  • 365 Pierce JP, Stefanick ML, Flatt SW et al. Greater survival after breast cancer in physically active women with high vegetable-fruit intake regardless of obesity. J Clin Oncol 2007; 25: 2345-2351
  • 366 Rock CL, Flatt SW, Natarajan L et al. Plasma carotenoids and recurrence-free survival in women with a history of breast cancer. J Clin Oncol 2005; 23: 6631-6638
  • 367 Chlebowski RT, Blackburn GL, Thomson CA et al. Dietary fat reduction and breast cancer outcome: interim efficacy results from the Women's Intervention Nutrition Study. J Natl Cancer Inst 2006; 98: 1767-1776
  • 368 Pierce JP, Natarajan L, Caan BJ et al. Influence of a diet very high in vegetables, fruit, and fiber and low in fat on prognosis following treatment for breast cancer: the Women’s Healthy Eating and Living (WHEL) randomized trial. JAMA 2007; 298: 289-298
  • 369 Thomson CA, Rock CL, Thompson PA et al. Vegetable intake is associated with reduced breast cancer recurrence in tamoxifen users: a secondary analysis from the Women’s Healthy Eating and Living Study. Breast Cancer Res Treat 2011; 125: 519-527
  • 370 Dansinger ML, Gleason JA, Griffith JL et al. Comparison of the Atkins, Ornish, Weight Watchers, and Zone diets for weight loss and heart disease risk reduction: a randomized trial. JAMA 2005; 293: 43-53
  • 371 Ye F, Li XJ, Jiang WL et al. Efficacy of and patient compliance with a ketogenic diet in adults with intractable epilepsy: a meta-analysis. J Clin Neurol 2015; 11: 26-31
  • 372 Wang X, Ouyang Y, Liu J et al. Fruit and vegetable consumption and mortality from all causes, cardiovascular disease, and cancer: systematic review and dose-response meta-analysis of prospective cohort studies. BMJ 2014; 349: g4490
  • 373 Gonzalez CA, Riboli E. Diet and cancer prevention: where we are, where we are going. Nutr Cancer 2006; 56: 225-231
  • 374 Bradbury KE, Appleby PN, Key TJ. Fruit, vegetable, and fiber intake in relation to cancer risk: findings from the European Prospective Investigation into Cancer and Nutrition (EPIC). Am J Clin Nutr 2014; 100 (Suppl. 01) 394S-398S
  • 375 World Cancer Research Fund and American Institute for Cancer Research. Food, nutrition, physical activity, and the prevention of cancer: a global perspective. Washington DC: AICR; 2007
  • 376 Farvid MS, Cho E, Chen WY et al. Dietary protein sources in early adulthood and breast cancer incidence: prospective cohort study. BMJ 2014; 348: g3437
  • 377 Sinha R, Cross AJ, Graubard BI et al. Meat intake and mortality: a prospective study of over half a million people. Arch Intern Med 2009; 169: 562-571
  • 378 Boffetta P, Couto E, Wichmann J et al. Fruit and vegetable intake and overall cancer risk in the European Prospective Investigation into Cancer and Nutrition (EPIC). J Natl Cancer Inst 2010; 102: 529-537
  • 379 Horneber M, Bueschel G, Dennert G et al. How many cancer patients use complementary and alternative medicine: a systematic review and metaanalysis. Integr Cancer Ther 2012; 11: 187-203
  • 380 Farina EK, Austin KG, Lieberman HR. Concomitant dietary supplement and prescription medication use is prevalent among US adults with doctor-informed medical conditions. J Acad Nutr Diet 2014; 114: 1784-1790, e2
  • 381 Bjelakovic G, Nikolova D, Gluud LL et al. Mortality in randomized trials of antioxidant supplements for primary and secondary prevention: systematic review and meta-analysis. JAMA 2007; 297: 842-857
  • 382 Lawson KA, Wright ME, Subar A et al. Multivitamin use and risk of prostate cancer in the National Institutes of Health-AARP Diet and Health Study. J Natl Cancer Inst 2007; 99: 754-764
  • 383 Ristow M, Zarse K, Oberbach A et al. Antioxidants prevent health-promoting effects of physical exercise in humans. Proc Natl Acad Sci U S A 2009; 106: 8665-8670
  • 384 The ATBC Cancer Prevention Study Group. The alpha-tocopherol, beta-carotene lung cancer prevention study: design, methods, participant characteristics, and compliance. Ann Epidemiol 1994; 4: 1-10
  • 385 Kenfield SA, Van Blarigan EL, DuPre N et al. Selenium supplementation and prostate cancer mortality. J Natl Cancer Inst 2014; 107: 360
  • 386 Wang L, Sesso HD, Glynn RJ et al. Vitamin E and C supplementation and risk of cancer in men: posttrial follow-up in the Physicians’ Health Study II randomized trial. Am J Clin Nutr 2014; 100: 915-923
  • 387 Rose AA, Elser C, Ennis M et al. Blood levels of vitamin D and early stage breast cancer prognosis: a systematic review and meta-analysis. Breast Cancer Res Treat 2013; 141: 331-339
  • 388 Autier P, Boniol M, Pizot C et al. Vitamin D status and ill health – author’s reply. Lancet Diabetes Endocrinol 2014; 2: 275-276
  • 389 Bolland MJ, Grey A, Gamble GD et al. The effect of vitamin D supplementation on skeletal, vascular, or cancer outcomes: a trial sequential meta-analysis. Lancet Diabetes Endocrinol 2014; 2: 307-320
  • 390 Koretz RL, Lipman TO, Klein S et al. AGA technical review on parenteral nutrition. Gastroenterology 2001; 121: 970-1001
  • 391 Amano K, Morita T, Baba M et al. Effect of nutritional support on terminally ill patients with cancer in a palliative care unit. Am J Hosp Palliat Care 2013; 30: 730-733
  • 392 Lundholm K, Daneryd P, Bosaeus I et al. Palliative nutritional intervention in addition to cyclooxygenase and erythropoietin treatment for patients with malignant disease: Effects on survival, metabolism, and function. Cancer 2004; 100: 1967-1977
  • 393 Soo I, Gramlich L. Use of parenteral nutrition in patients with advanced cancer. Appl Physiol Nutr Metab 2008; 33: 102-106
  • 394 Cozzaglio L, Balzola F, Cosentino F et al. Outcome of cancer patients receiving home parenteral nutrition. Italian Society of Parenteral and Enteral Nutrition (S.I.N.P.E.). JPEN J Parenter Enteral Nutr 1997; 21: 339-342
  • 395 August DA, Huhmann MB. American Society for Parenteral and Enteral Nutrition (A.S.P.E.N.) Board of Directors. A.S.P.E.N. clinical guidelines: nutrition support therapy during adult anticancer treatment and in hematopoietic cell transplantation. JPEN J Parenter Enteral Nutr 2009; 33: 472-500
  • 396 Gripp S, Moeller S, Bolke E et al. Survival prediction in terminally ill cancer patients by clinical estimates, laboratory tests, and self-rated anxiety and depression. J Clin Oncol 2007; 25: 3313-3320
  • 397 Bozzetti F, Santarpia L, Pironi L et al. The prognosis of incurable cachectic cancer patients on home parenteral nutrition: a multi-centre observational study with prospective follow-up of 414 patients. Ann Oncol 2014; 25: 487-493
  • 398 Bundesärztekammer. Grundsätze der Bundesärztekammer zur ärztlichen Sterbebegleitung. Deutsches Ärzteblatt 2011; 108: A346-A348
  • 399 McCann RM, Hall WJ, Groth-Juncker A. Comfort care for terminally ill patients. The appropriate use of nutrition and hydration. JAMA 1994; 272: 1263-1266
  • 400 Bruera E, Hui D, Dalal S et al. Parenteral hydration in patients with advanced cancer: a multicenter, double-blind, placebo-controlled randomized trial. J Clin Oncol 2013; 31: 111-118
  • 401 Cohen MZ, Torres-Vigil I, Burbach BE et al. The meaning of parenteral hydration to family caregivers and patients with advanced cancer receiving hospice care. J Pain Symptom Manage 2012; 43: 855-865
  • 402 Lawlor PG, Gagnon B, Mancini IL et al. Occurrence, causes, and outcome of delirium in patients with advanced cancer: a prospective study. Arch Intern Med 2000; 160: 786-794
  • 403 Bruera E, Sala R, Rico MA et al. Effects of parenteral hydration in terminally ill cancer patients: a preliminary study. J Clin Oncol 2005; 23: 2366-2371
  • 404 Fainsinger RL, Bruera E. When to treat dehydration in a terminally ill patient?. Support Care Cancer 1997; 5: 205-211