Evolution of BCL-2/IgH hybrid gene RNA expression during treatment of T(14;18)-bearing follicular lymphomas

Br J Cancer. 1999 Nov;81(5):860-9. doi: 10.1038/sj.bjc.6690777.

Abstract

Bcl-2, the gene over-expressed in follicular lymphomas (FL), is able to block chemotherapy-induced apoptosis. Consequently, we wondered whether bcl-2/IgH expression variations during treatment of FL could predict the outcome of patients with t(14;18)-bearing FL. For this purpose, we used a reverse transcription polymerase chain reaction (RT-PCR) assay to analyse 180 serial peripheral blood samples (PBS) during 34 treatment phases in 25 patients with t(14;18)-bearing FL. In all patients but two, bcl-2/IgH gene expression was demonstrated in pre-treatment samples. During 16 out of the 34 treatment phases (47%), bcl-2/IgH expression became negative: all but one were responders to chemotherapy. This conversion was transient in six cases. In 18 treatment phases, bcl2/IgH expression remained detectable: eight were clinically considered as treatment failures, while eight others achieved PR and two achieved CR. We observed a significant correlation between treatment response and RNA PCR results (P = 0.002). Three-year overall survival of patients with stable bcl2/IgH-negative conversion was 100% compared to 54% for the remaining patients (P = 0.069); 3-year freedom from progression was respectively 87.5% and 13% (P = 0.005). These results indicate a correlation between bcl-2/IgH expression variations and both clinical response and outcome. Whether this might predict disease outcome early remains to be confirmed.

Publication types

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

MeSH terms

  • Adult
  • Aged
  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use
  • Base Sequence
  • Chromosomes, Human, Pair 14*
  • Chromosomes, Human, Pair 18*
  • Humans
  • Immunoglobulin Heavy Chains / genetics*
  • Lymphoma, Follicular / blood
  • Lymphoma, Follicular / genetics*
  • Lymphoma, Follicular / pathology
  • Lymphoma, Follicular / therapy*
  • Middle Aged
  • Molecular Sequence Data
  • Neoplastic Cells, Circulating / metabolism
  • Prospective Studies
  • Proto-Oncogene Proteins c-bcl-2 / genetics*
  • RNA, Neoplasm / biosynthesis*
  • Survival Analysis
  • Translocation, Genetic*

Substances

  • Immunoglobulin Heavy Chains
  • Proto-Oncogene Proteins c-bcl-2
  • RNA, Neoplasm