Eur J Pediatr Surg 2021; 31(04): 362-366
DOI: 10.1055/s-0040-1714658
Original Article

Implication of Image-Defined Risk Factors for the Extent of Surgical Resection and Clinical Outcome in Patients with Pelvic Neuroblastoma

Alexandra Froeba-Pohl
1   Department of Pediatric Surgery, Munich University Hospital Dr. von Hauner Children's Hospital, Munich, Germany
,
Dietrich von Schweinitz
1   Department of Pediatric Surgery, Munich University Hospital Dr. von Hauner Children's Hospital, Munich, Germany
,
Jakob Muehling
1   Department of Pediatric Surgery, Munich University Hospital Dr. von Hauner Children's Hospital, Munich, Germany
,
Marco Paolini
2   Department of Radiology, University Hospital Munich, Munich, Germany
,
Jochen Hubertus
1   Department of Pediatric Surgery, Munich University Hospital Dr. von Hauner Children's Hospital, Munich, Germany
› Author Affiliations

Abstract

Introduction Pelvic neuroblastoma (NB) is a rare entity and occurs in 2 to 5% of all NBs. Surgery in the pelvic area is—even for the experienced oncological surgeon—technically challenging, as injuries of bladder and/or rectal innervation may carry lifelong consequences for the patient. Several studies have proven the impact of image-defined risk factors (IDRFs) for outcome, complications and extent of resection in NB; however, the specific role of IDRF in pelvic NB has not been investigated yet.

Materials and Methods Patient charts were retrospectively evaluated for International Staging System stage, IDRF status, MYCN amplification, and outcome parameters.

Results Between 2003 and 2019, 277 NBs were surgically resected in the department of pediatric surgery of Dr. von Hauner Children's Hospital. Out of these, 11 patients (3.9%) had pelvic NB. Evaluation of the preoperative imaging showed two patients without IDRF (stage L1) and eight patients in stage L2. One patient had stage M according to distant metastasis. Patients without IDRF underwent complete macroscopical resections, whereas complete tumor removal was not possible without mutilation in patients with IDRF. At time point of diagnosis, only patients with IDRF had functional neurological problems. Three patients developed perioperative complications; all of them had at least one IDRF. Three patients developed local recurrence during the course of the disease, all of them had at least one IDRF.

Conclusion Our results indicate on a preliminary level the importance of IDRF as a prognostic tool for surgical removal of pelvic NB.



Publication History

Received: 13 March 2020

Accepted: 18 June 2020

Article published online:
30 August 2020

© 2020. Thieme. All rights reserved.

Georg Thieme Verlag KG
Rüdigerstraße 14, 70469 Stuttgart, Germany

 
  • References

  • 1 Irwin MS, Park JR. Neuroblastoma: paradigm for precision medicine. Pediatr Clin North Am 2015; 62 (01) 225-256
  • 2 Vo KT, Matthay KK, Neuhaus J. et al. Clinical, biologic, and prognostic differences on the basis of primary tumor site in neuroblastoma: a report from the International Neuroblastoma Risk Group project. J Clin Oncol 2014; 32 (28) 3169-3176
  • 3 Leclair MD, Hartmann O, Heloury Y. et al. Localized pelvic neuroblastoma: excellent survival and low morbidity with tailored therapy--the 10-year experience of the French Society of Pediatric Oncology. J Clin Oncol 2004; 22 (09) 1689-1695
  • 4 Irtan S, Brisse HJ, Minard-Colin V, Schleiermacher G, Canale S, Sarnacki S. Minimally invasive surgery of neuroblastic tumors in children: indications depend on anatomical location and image-defined risk factors. Pediatr Blood Cancer 2015; 62 (02) 257-261
  • 5 Kraal K, Blom T, van Noesel M. et al. Treatment and outcome of neuroblastoma with intraspinal extension: a systematic review. Pediatr Blood Cancer 2017;64(08):
  • 6 Kraal K, Blom T, Tytgat L. et al. Neuroblastoma with intraspinal extension: health problems in long-term survivors. Pediatr Blood Cancer 2016; 63 (06) 990-996
  • 7 Cruccetti A, Kiely EM, Spitz L, Drake DP, Pritchard J, Pierro A. Pelvic neuroblastoma: low mortality and high morbidity. J Pediatr Surg 2000; 35 (05) 724-728
  • 8 Haase GM, O'Leary MC, Stram DO. et al. Pelvic neuroblastoma--implications for a new favorable subgroup: a Children's Cancer Group experience. Ann Surg Oncol 1995; 2 (06) 516-523
  • 9 Cohn SL, Pearson AD, London WB. et al; INRG Task Force. The International Neuroblastoma Risk Group (INRG) classification system: an INRG Task Force report. J Clin Oncol 2009; 27 (02) 289-297
  • 10 Monclair T, Brodeur GM, Ambros PF. et al; INRG Task Force. The International Neuroblastoma Risk Group (INRG) staging system: an INRG Task Force report. J Clin Oncol 2009; 27 (02) 298-303
  • 11 Iehara T, Yoneda A, Yokota I. et al; Japan Childhood Cancer Group Neuroblastoma Committee (JNBSG). Results of a prospective clinical trial JN-L-10 using image-defined risk factors to inform surgical decisions for children with low-risk neuroblastoma disease: A report from the Japan Children's Cancer Group Neuroblastoma Committee. Pediatr Blood Cancer 2019; 66 (11) e27914
  • 12 Pohl A, Erichsen M, Stehr M. et al. Image-defined risk factors correlate with surgical radicality and local recurrence in patients with neuroblastoma. Klin Padiatr 2016; 228 (03) 118-123
  • 13 Monclair T, Mosseri V, Cecchetto G, De Bernardi B, Michon J, Holmes K. Influence of image-defined risk factors on the outcome of patients with localised neuroblastoma. A report from the LNESG1 study of the European International Society of Paediatric Oncology Neuroblastoma Group. Pediatr Blood Cancer 2015; 62 (09) 1536-1542
  • 14 Simon T, Häberle B, Hero B, von Schweinitz D, Berthold F. Role of surgery in the treatment of patients with stage 4 neuroblastoma age 18 months or older at diagnosis. J Clin Oncol 2013; 31 (06) 752-758
  • 15 Cotterill SJ, Pearson AD, Pritchard J. et al. Clinical prognostic factors in 1277 patients with neuroblastoma: results of The European Neuroblastoma Study Group ‘Survey’ 1982-1992. Eur J Cancer 2000; 36 (07) 901-908
  • 16 Günther P, Holland-Cunz S, Schupp CJ, Stockklausner C, Hinz U, Schenk JP. Significance of image-defined risk factors for surgical complications in patients with abdominal neuroblastoma. Eur J Pediatr Surg 2011; 21 (05) 314-317
  • 17 Phelps HM, Ndolo JM, Van Arendonk KJ. et al. Association between image-defined risk factors and neuroblastoma outcomes. J Pediatr Surg 2019; 54 (06) 1184-1191
  • 18 Avanzini S, Pio L, Erminio G. et al. Image-defined risk factors in unresectable neuroblastoma: SIOPEN study on incidence, chemotherapy-induced variation, and impact on surgical outcomes. Pediatr Blood Cancer 2017; 64 (11) e26605
  • 19 Günther P, Tröger J, Holland-Cunz S. et al. Surgical complications in abdominal tumor surgery in children. Experiences at a single oncological center. Eur J Pediatr Surg 2009; 19 (05) 297-303
  • 20 Zobel M, Zamora A, Sura A. et al. The clinical management and outcomes of pelvic neuroblastic tumors. J Surg Res 2020; 249: 8-12
  • 21 Katzenstein HM, Kent PM, London WB, Cohn SL. Treatment and outcome of 83 children with intraspinal neuroblastoma: the Pediatric Oncology Group experience. J Clin Oncol 2001; 19 (04) 1047-1055