Competitive polymerase chain reaction for the determination of N-myc amplification in neuroblastoma: report of clinical cases

Eur J Pediatr Surg. 1999 Jun;9(3):138-41. doi: 10.1055/s-2008-1072229.

Abstract

If an unfavorable prognosis is suspected in neuroblastoma, decision on a treatment protocol should be based on the N-myc copy number (12). We already demonstrated that the newly developed competitive polymerase chain reaction (competitive PCR) is a promising method for the determination of the N-myc copy number (6), and have started to use this competitive PCR procedure in neuroblastoma patients, together with fine-needle biopsy in selected cases. Seven children were studied. In one infant of 5 months of age whose tumor was diagnosed before undergoing mass screening for neuroblastoma, the competitive PCR procedure was performed with a fine-needle biopsy, and after obtaining a negative report on N-myc amplification within 48 hours, a regular protocol of treatment could be started without delay. We report that competitive PCR is a rapid and accurate method for the determination of the N-myc copy number, requiring only a small amount of material, and anticipate that competitive PCR will become the procedure of choice for the determination of N-myc copy number in neuroblastoma.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adrenal Gland Neoplasms / genetics
  • Adrenal Gland Neoplasms / pathology
  • Biopsy, Needle
  • Child
  • Child, Preschool
  • Female
  • Gene Amplification / genetics*
  • Gene Expression Regulation, Neoplastic / physiology
  • Humans
  • Infant
  • Infant, Newborn
  • Male
  • Mediastinal Neoplasms / genetics
  • Mediastinal Neoplasms / pathology
  • Neoplasm Staging
  • Neuroblastoma / genetics*
  • Neuroblastoma / pathology
  • Polymerase Chain Reaction / methods*
  • Prognosis
  • Proto-Oncogene Proteins c-myc / genetics*
  • Retroperitoneal Neoplasms / genetics
  • Retroperitoneal Neoplasms / pathology
  • Soft Tissue Neoplasms / genetics*
  • Soft Tissue Neoplasms / pathology

Substances

  • Proto-Oncogene Proteins c-myc