Peripheral blood stem cell tumor cell contamination and survival of neuroblastoma patients

Clin Cancer Res. 2006 Oct 1;12(19):5680-5. doi: 10.1158/1078-0432.CCR-06-0740.

Abstract

Purpose: Contribution of peripheral blood stem cell (PBSC) contaminating tumor cells to subsequent relapse and overall survival of neuroblastoma patients remains controversial.

Experimental design: Neuroblastoma cell contamination of 27 PBSC harvests from stage IV neuroblastoma patients was assessed by quantitative RT-PCR for both tyrosine hydroxylase (TH) and GD2 synthase (GD2-s). The effect of PBSC contamination on survival was then analyzed.

Results: Seven PBSC tested negative for both markers; 19 were positive for GD2-s, 6 for TH, with 5 positive for both. Survival of the 20 patients with positive PBSC did not differ from that of the patients with negative PBSC (log-rank test, P = 0.134 and 0.218 for event-free survival and overall survival, respectively). By considering the TH and GD2-s results independently, a borderline (P = 0.053) negative effect on event-free survival was observed in patients reinfused with GD2-s-positive PBSC. When the status at transplant was taken into account, only the event-free survival of the patients rescued when in complete remission with GD2-s-negative PBSC was better, although not significantly, than that of patients infused with GD2-s-positive PBSC.

Conclusions: Our results obtained in a small cohort of homogeneously treated stage IV patients suggest that patient survival is not affected by PBSC contamination with the exception of a borderline negative effect on event-free survival in patients rescued when in complete remission.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bone Marrow Purging / methods
  • Cell Separation / methods
  • Child, Preschool
  • Disease-Free Survival
  • Female
  • Hematopoietic Stem Cells / pathology*
  • Humans
  • Male
  • N-Acetylgalactosaminyltransferases / genetics*
  • N-Acetylgalactosaminyltransferases / metabolism
  • Neoplastic Cells, Circulating / pathology*
  • Neuroblastoma / enzymology
  • Neuroblastoma / mortality*
  • Neuroblastoma / therapy
  • Polymerase Chain Reaction / methods
  • RNA, Neoplasm / genetics
  • RNA, Neoplasm / metabolism
  • Survival Rate
  • Transplantation, Autologous
  • Tyrosine 3-Monooxygenase / genetics*
  • Tyrosine 3-Monooxygenase / metabolism

Substances

  • RNA, Neoplasm
  • Tyrosine 3-Monooxygenase
  • N-Acetylgalactosaminyltransferases
  • (N-acetylneuraminyl)-galactosylglucosylceramide N-acetylgalactosaminyltransferase