European Journal of Cancer
Volume 45, Issue 1 , Pages 90-98, January 2009

Management and outcome of stage 3 neuroblastoma

  • Shakeel Modak

      Affiliations

    • Department of Paediatrics, Memorial Sloan-Kettering Cancer Center, 1275 York Avenue, New York, NY 10065, United States
    • Corresponding Author InformationCorresponding author: Tel.: +1 212 639 7623; fax: +1 212 717 3695.
  • ,
  • Brian H. Kushner

      Affiliations

    • Department of Paediatrics, Memorial Sloan-Kettering Cancer Center, 1275 York Avenue, New York, NY 10065, United States
    • Tel.: +1 212 639 6793
  • ,
  • Michael P. LaQuaglia

      Affiliations

    • Department of Surgery, Memorial Sloan-Kettering Cancer Center, 1275 York Avenue, New York, NY 10065, United States
    • Tel.: +1 212 639 7002
  • ,
  • Kim Kramer

      Affiliations

    • Department of Paediatrics, Memorial Sloan-Kettering Cancer Center, 1275 York Avenue, New York, NY 10065, United States
    • Tel.: +1 212 639 6410
  • ,
  • Nai-Kong V. Cheung

      Affiliations

    • Department of Paediatrics, Memorial Sloan-Kettering Cancer Center, 1275 York Avenue, New York, NY 10065, United States
    • Tel.: +1 646 888 2313

Received 17 July 2008; received in revised form 24 August 2008; accepted 25 September 2008. published online 10 November 2008.

Abstract 

Purpose

The management of patients with International Neuroblastoma Staging System (INSS) stage 3 neuroblastoma (NB) is not consistent worldwide. We describe a single centre approach at Memorial Sloan-Kettering Cancer Centre (MSKCC) from 1991 to 2007 that minimises therapy except for those patients with MYCN-amplified NB.

Methods

In this retrospective analysis of 69 patients, tumour MYCN was not amplified in 53 and amplified in 16. Event-free survival (EFS) and overall survival (OS) were determined by Kaplan–Meier analysis.

Results

Fourteen patients with non-MYCN-amplified tumours were treated with surgery alone (group A) and the remaining 39 (group B) with surgery following chemotherapy that was initiated and administered at non-MSKCC institutions. Chemotherapy was discontinued after surgery in 38/39 of the latter. The 10-year EFS and OS for all patients with MYCN-non-amplified NB were 74.9±16.9% and 92.6±5.5%, respectively. There was no difference in OS between groups A and B (p=0.2; 10-year OS for groups A and B was 84.6±14% and 97.1±2.9%, respectively). Patients with MYCN-amplified disease (group C) underwent dose-intensive induction, tumour resection and local radiotherapy: 13 achieved complete or very good partial remission, and 10 received myeloablative chemotherapy. 11/16 patients also received 3F8-based immunotherapy: 10 remain free of disease. The 10-year EFS and OS for patients with MYCN-amplified neuroblastoma treated with immunotherapy were both 90.9±8.7%.

Conclusion

Patients with MYCN-non-amplified stage 3 NB can be successfully treated with surgery without the need for radiotherapy or continuation of chemotherapy. Combination of dose-intensive chemotherapy, surgery, radiotherapy and immunotherapy was associated with a favourable outcome for most patients with MYCN-amplified stage 3 NB.

Keywords: Stage 3 neuroblastoma, Immunotherapy, Prognosis

 

PII: S0959-8049(08)00748-X

doi:10.1016/j.ejca.2008.09.016

European Journal of Cancer
Volume 45, Issue 1 , Pages 90-98, January 2009