Angewandte Nuklearmedizin 2022; 45(01): 28-34
DOI: 10.1055/a-1666-2526
Update Lymphome
Übersicht

Rolle der PET/CT beim multiplen Myelom und anderen Plasmazellerkrankungen

Role of PET/CT in the diagnosis and management of multiple myeloma and other plasma cell disorders
Thorsten Derlin
1   Klinik für Nuklearmedizin, Medizinische Hochschule Hannover, Hannover
,
Christian Pfob
2   Klinik für Nuklearmedizin, Universitätsklinikum Augsburg
,
Constantin Lapa
2   Klinik für Nuklearmedizin, Universitätsklinikum Augsburg
› Institutsangaben

Zusammenfassung

Die 18F-Fluordesoxyglukose (FDG) Positronen-Emissions-Tomografie/Computertomografie (PET/CT) als Verfahren der molekularen Bildgebung erlaubt die simultane Beurteilung morphologischer Charakteristika des mineralisierten Knochens (z. B. Osteolysen) sowie molekularer Parameter (z. B. Stoffwechselaktivität) und bietet damit umfassende (patho)biologische Informationen. Sie hat in den letzten Jahren einen zunehmend wichtigen Stellenwert in der Bildgebung der Plasmazellerkrankungen gefunden, ist zentrales Instrument sowohl in der Differenzialdiagnostik als auch in der Ausbreitungsdiagnostik der einzelnen Entitäten und erlaubt ein Therapiemonitoring im Verlauf. In der Initialdiagnostik leistet die FDG PET/CT einen wertvollen Beitrag in der Differenzialdiagnostik der Plasmazellerkrankungen, insbesondere beim solitären Plasmozytom. Zudem ermöglicht sie eine sensitive Ausbreitungsdiagnostik beim multiplen Myelom durch die Erfassung eines fokalen und diffusen Knochenmarkbefalls sowie para- und extramedullärer Myelommanifestationen. Die FDG PET/CT ist dabei dem konventionellen Röntgenstatus und der low-dose Computertomografie (LDCT) überlegen und der Ganzkörper-Magnetresonanztomografie (GK-MRT) weitestgehend gleichwertig. Sie liefert zudem prognostische Informationen, insbesondere vor Stammzelltransplantation, und ist aufgrund ihres hohen positiv prädiktiven Wertes bildgebender Referenzstandard zur Beurteilung des Therapieansprechens. Zudem kann sie zusammen mit anderen Methoden eingesetzt werden, um eine minimale Resterkrankung (MRD)-Negativität zu definieren. Neue Radiopharmaka und theranostische Ansätze erweitern das Einsatzfeld für die PET bei Plasmazellerkrankungen.

Abstract

Molecular imaging by 18F-fluorodeoxyglucose (FDG) positron emission tomography/computed tomography (PET/CT) allows for simultaneous assessment of morphologic characteristics of mineralized bone (e. g., osteolysis) as well as molecular parameters (e. g., glucose metabolism), thereby providing comprehensive (patho)biological information. In recent years, FDG PET/CT has found its well-defined role in imaging plasma cell disorders and has become an indispensable instrument for differential diagnosis and staging of the respective entities. It also allows for therapy monitoring in the course of the disease. In initial diagnosis, FDG PET/CT decisively contributes to establishing the differential diagnosis of plasma cell disorders, particularly in solitary plasmacytoma. In addition, it provides a sensitive staging method detecting both focal and diffuse bone marrow involvement as well as paramedullary and extramedullary myeloma lesions. FDG PET/CT is superior to both conventional whole-body x-ray (WBXR) and low-dose computed tomography (LDCT), and equals the performance of whole-body magnetic resonance imaging (WB-MRI). FDG PET also provides prognostic information, in particular before hematopoietic stem cell transplantation. PET has become the preferred imaging method for therapy response assessment due to its high positive predictive value. Moreover, PET may be applied in conjunction with other methods to define minimal residual disease (MRD)-negativity. Novel radiopharmaceuticals and theranostic approaches broaden the role for PET in plasma cell disorders.



Publikationsverlauf

Artikel online veröffentlicht:
07. März 2022

© 2022. Thieme. All rights reserved.

Georg Thieme Verlag KG
Rüdigerstraße 14, 70469 Stuttgart, Germany

 
  • Literaturverzeichnis

  • 1 Nair B, Waheed S, Szymonifka J. et al. Immunoglobulin isotypes in multiple myeloma: laboratory correlates and prognostic implications in total therapy protocols. Br J Haematol 2009; 145: 134-137
  • 2 Kyle RA, Gertz MA, Witzig TE. et al. Review of 1027 patients with newly diagnosed multiple myeloma. Mayo Clin Proc 2003; 78: 21-33
  • 3 Rajkumar SV, Dimopoulos MA, Palumbo A. et al. International Myeloma Working Group updated criteria for the diagnosis of multiple myeloma. Lancet Oncol 2014; 15: e538-548
  • 4 McKenna RW, Kyle RA, Kuehl WM. et al. WHO Classification of Tumours of Haematopoietic and Lymphoid Tissues, 4th edit update. Swerdlow SH, Campo E, Harris NL, Jaffe ES, Pileri SA, Stein H, Thiele J. Lyon: IARC; 2017: 241-253
  • 5 Bird SA, Boyd K. Multiple myeloma: an overview of management. Palliat Care Soc Pract 2019; DOI: 10.1177/1178224219868235 .
  • 6 Gerecke C, Fuhrmann S, Strifler S. et al. The Diagnosis and Treatment of Multiple Myeloma. Dtsch Arztebl Int 2016; 113: 470-476
  • 7 Dimopoulos M, Terpos E, Comenzo RL. et al. International myeloma working group consensus statement and guidelines regarding the current role of imaging techniques in the diagnosis and monitoring of multiple Myeloma. Leukemia 2009; 23: 1545-1556
  • 8 Mateos MV, Hernández MT, Giraldo P. et al. Lenalidomide plus dexamethasone for high-risk smoldering multiple myeloma. N Engl J Med 2013; 369: 438-447
  • 9 Kastritis E, Moulopoulos LA, Terpos E. et al. The prognostic importance of the presence of more than one focal lesion in spine MRI of patients with asymptomatic (smoldering) multiple myeloma. Leukemia 2014; 28: 2402-2403
  • 10 Cavo M, Terpos E, Nanni C. et al. Role of (18)F-FDG PET/CT in the diagnosis and management of multiple myeloma and other plasma cell disorders: a consensus statement by the International Myeloma Working Group. Lancet Oncol 2017; 18: e206-217
  • 11 Zamagni E, Nanni C, Gay F. et al. 18F-FDG PET/CT focal, but not osteolytic, lesions predict the progression of smoldering myeloma to active disease. Leukemia 2016; 30: 417-422
  • 12 Siontis B, Kumar S, Dispenzieri A. et al. Positron emission tomography-computed tomography in the diagnostic evaluation of smoldering multiple myeloma: identification of patients needing therapy. Blood Cancer J 2015; 5: e364
  • 13 Salaun PY, Gastinne T, Frampas E. et al. FDG-positron-emission tomography for staging and therapeutic assessment in patients with plasmacytoma. Haematologica 2008; 93: 1269-1271
  • 14 Albano D, Bosio G, Treglia G. et al. 18F-FDG PET/CT in solitary plasmacytoma: metabolic behavior and progression to multiple myeloma. Eur J Nucl Med Mol Imaging 2018; 45: 77-84
  • 15 Nanni C, Zamagni E, Farsad M. et al. Role of 18F-FDG PET/CT in the assessment of bone involvement in newly diagnosed multiple myeloma: preliminary results. Eur J Nucl Med Mol Imaging 2006; 33: 525-531
  • 16 Moreau P, Attal M, Caillot D. et al. Prospective Evaluation of Magnetic Resonance Imaging and [18F]Fluorodeoxyglucose Positron Emission Tomography-Computed Tomography at Diagnosis and Before Maintenance Therapy in Symptomatic Patients With Multiple Myeloma Included in the IFM/DFCI 2009 Trial: Results of the IMAJEM Study. J Clin Oncol 2017; 35: 2911-2918
  • 17 Lu YY, Chen JH, Lin WY. et al. FDG PET or PET/CT for detecting intramedullary and extramedullary lesions in multiple Myeloma: a systematic review and meta-analysis. Clin Nucl Med 2012; 37: 833-837
  • 18 Zamagni E, Patriarca F, Nanni C. et al. Prognostic relevance of 18-F FDG PET/CT in newly diagnosed multiple myeloma patients treated with up-front autologous transplantation. Blood 2011; 118: 5989-5995
  • 19 Bartel TB, Haessler J, Brown TL. et al. F18-fluorodeoxyglucose positron emission tomography in the context of other imaging techniques and prognostic factors in multiple myeloma. Blood 2009; 114: 2068-2076
  • 20 Bannas P, Kröger N, Adam G. et al. [Modern imaging techniques in patients with multiple myeloma]. Rofo 2013; 185: 26-33
  • 21 Wahlin A, Holm J, Osterman G. et al. Evaluation of serial bone X-ray examination in multiple myeloma. Acta Med Scand 1982; 212: 385-387
  • 22 Derlin T, Peldschus K, Münster S. et al. Comparative diagnostic performance of ¹⁸F-FDG PET/CT versus whole-body MRI for determination of remission status in multiple myeloma after stem cell transplantation. Eur Radiol 2013; 23: 570-578
  • 23 Davies FE, Rosenthal A, Rasche L. et al. Treatment to suppression of focal lesions on positron emission tomography-computed tomography is a therapeutic goal in newly diagnosed multiple myeloma. Haematologica 2018; 103: 1047-1053
  • 24 Hillengass J, Usmani S, Rajkumar SV. et al. International myeloma working group consensus recommendations on imaging in monoclonal plasma cell disorders. Lancet Oncol 2019; 20: e302-e312
  • 25 Zamagni E, Tacchetti P, Barbato S. et al. Role of Imaging in the Evaluation of Minimal Residual Disease in Multiple Myeloma Patients. J Clin Med 2020; 9: 3519
  • 26 Zamagni E, Nanni C, Dozza L. et al. Standardization of 18F-FDG-PET/CT According to Deauville Criteria for Metabolic Complete Response Definition in Newly Diagnosed Multiple Myeloma. J Clin Oncol 2021; 39: 116-125
  • 27 Rasche L, Angtuaco E, McDonald JE. et al. Low expression of hexokinase-2 is associated with false-negative FDG-positron emission tomography in multiple myeloma. Blood 2017; 130: 30-34
  • 28 Sachpekidis C, Mai EK, Goldschmidt H. et al. (18)F-FDG dynamic PET/CT in patients with multiple myeloma: patterns of tracer uptake and correlation with bone marrow plasma cell infiltration rate. Clin Nucl Med 2015; 40: e300-307
  • 29 Pan Q, Cao X, Luo Y. et al. Chemokine receptor-4 targeted PET/CT with 68Ga-Pentixafor in assessment of newly diagnosed multiple myeloma: comparison to 18F-FDG PET/CT. Eur J Nucl Med Mol Imaging 2020; 47: 537-546
  • 30 Lapa C, Schreder M, Schirbel A. et al. [68Ga]Pentixafor-PET/CT for imaging of chemokine receptor CXCR4 expression in multiple myeloma - Comparison to [18F]FDG and laboratory values. Theranostics 2017; 7: 205-212
  • 31 Lapa C, Lückerath K, Kircher S. et al. Potential influence of concomitant chemotherapy on CXCR4 expression in receptor directed endoradiotherapy. Br J Haematol 2019; 184: 440-443
  • 32 Lapa C, Herrmann K, Schirbel A. et al. CXCR4-directed endoradiotherapy induces high response rates in extramedullary relapsed Multiple Myeloma. Theranostics 2017; 7: 1589-1597