Comparison of toxicity following different conditioning regimens (busulfan/melphalan and carboplatin/etoposide/melphalan) for advanced stage neuroblastoma: Experience of two transplant centers

Pediatr Transplant. 2016 Mar;20(2):284-9. doi: 10.1111/petr.12638. Epub 2015 Nov 28.

Abstract

The outcome for advanced neuroblastoma has improved with combined modality therapy: induction chemotherapy, surgery, and consolidation with high-dose chemotherapy/autologous HSCT, followed by local radiation, cisretinoic acid, and recently antibody therapy. In the United States, the most common conditioning regimen is CEM, while in Europe/Middle East, Bu/Mel has been widely used; it remains unclear which regimen has the best outcome. Assess renal, hepatic, and infectious toxicity through Day+100 in 2 different regimens. Retrospective comparison between CEM-DFCHCC Boston and Bu/Mel- CCHE-57357. Thirty-five patients, median age 4, in Boston (2007-2011) and 38 patients, median age 3, in Cairo (2009-2011). Renal toxicity; creatinine was significantly higher in CEM than Bu/Mel: 57% (median day+90) vs. 29% (median>day+100), p = 0.004. One CEM patient died from renal dialysis at day+19. Hepatic toxicity was significantly higher in CEM than Bu/Mel: 80% (median day+26) vs. 58% (median day+60), p = 0.04. In infectious complications with CEM 14%, bacteremia (n = 4) and fungemia (n = 1), 3 had culture-negative sepsis requiring vasopressors. With Bu/Mel 18%, bacteremia (n = 7), none required pressors, p = 0.4. Bu/Mel was associated with less acute hepatic and renal toxicity and thus may be preferable for preserving organ functions.

Keywords: autologous hematopoietic stem cell transplantation (HSCT); busulfan/melphalan (Bu/Mel); carboplatin; etoposide; melphalan (CEM); neuroblastoma; renal toxicity.

Publication types

  • Comparative Study
  • Multicenter Study

MeSH terms

  • Adolescent
  • Antineoplastic Agents / administration & dosage
  • Boston
  • Brain Neoplasms / drug therapy
  • Brain Neoplasms / therapy*
  • Busulfan / administration & dosage*
  • Carboplatin / administration & dosage*
  • Child
  • Child, Preschool
  • Egypt
  • Etoposide / administration & dosage*
  • Humans
  • Infant
  • Infant, Newborn
  • Melphalan / administration & dosage*
  • Neuroblastoma / drug therapy
  • Neuroblastoma / therapy*
  • Retrospective Studies
  • Transplantation Conditioning / methods*
  • Treatment Outcome

Substances

  • Antineoplastic Agents
  • Etoposide
  • Carboplatin
  • Busulfan
  • Melphalan