Detection of EWS chimeric transcripts by nested RT-PCR to allow reinfusion of uncontaminated peripheral blood stem cells in high-risk Ewing's tumor in childhood

Haematologica. 1999 Nov;84(11):1012-5.

Abstract

Background and objective: Ewing's tumors (ET) are primary malignancies of bone and soft tissues characterized in at least 96% of cases by specific fusion transcripts originating from recurrent chromosomal translocations. Clinical protocols for high-risk metastatic ETs include high-dose radiation/chemotherapy followed by autologous peripheral blood stem cell (PBSC) reinfusion. We used nested reverse transcriptase polymerase chain reaction (RT-PCR) to search for the presence of ET-specific transcripts in PBSC collections from patients with high-risk ET in order to collect harvests free from neoplastic cells but still sufficient to obtain early stable engraftment.

Design and methods: Thirty-seven harvest samples from 15 ET patients treated with mobilizing chemotherapy were analyzed. Nested RT-PCR was performed to detect ET-specific transcripts in RNA extracted from the PBSC collections.

Results: A total of 30 harvests was performed. On average, 2 harvests (range 1-4) were sufficient to collect the minimum required number of mononuclear cells (2.5

Publication types

  • Clinical Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Child
  • Chromosomes, Human, Pair 11
  • Chromosomes, Human, Pair 22
  • Disease-Free Survival
  • Hematopoietic Stem Cell Transplantation / methods*
  • Humans
  • Oncogene Proteins, Fusion / analysis*
  • Oncogene Proteins, Fusion / genetics
  • Recombinant Fusion Proteins / analysis*
  • Recombinant Fusion Proteins / genetics
  • Recurrence
  • Reverse Transcriptase Polymerase Chain Reaction / methods*
  • Risk Factors
  • Sarcoma, Ewing / blood*
  • Sarcoma, Ewing / epidemiology
  • Sarcoma, Ewing / genetics*
  • Sensitivity and Specificity
  • Transcription, Genetic
  • Translocation, Genetic / genetics
  • Transplantation, Autologous

Substances

  • EWS-ETV1 fusion protein, human
  • Oncogene Proteins, Fusion
  • Recombinant Fusion Proteins