Intensive conventional-dose chemotherapy for stage IV low-grade lymphoma: high remission rates and reversion to negative of peripheral blood bcl-2 rearrangement

Ann Oncol. 1994:5 Suppl 2:73-7. doi: 10.1093/annonc/5.suppl_2.s73.

Abstract

Background: Advanced-stage low-grade lymphoma is characterized by initial responsiveness to many conventional therapies but ultimate relapse. Intensive therapy approaches with non-cross-resistant regimens have not been extensively explored. The polymerase chain reaction (PCR) can be used to monitor for the presence of cells with rearrangement of bcl-2, and provides a sensitive and stringent parameter of disease activity and treatment response that may have clinical utility.

Patients and methods: From 1988 to 1992, 138 evaluable patients were treated with 3 sequential chemotherapy regimens, as well as with interferon alfa 2b (IFN) in combination with corticosteroids. Nineteen patients had serial PCR monitoring for bcl-2 rearrangement.

Results: Among a subset of 58 patients who had an initial phase of IFN plus prednisone, the response rate was 59%, mostly partial remissions (PR). With the chemotherapy program, 65% have achieved complete remission to date, and 30% PR. By PCR analysis, 13 of 19 tested achieved negative status ('molecular remission'), a much higher frequency of molecular remission than has been seen with standard therapies, and these molecular remissions appear to correlate with a lower likelihood of relapse.

Conclusions: Intensive conventional-dose chemotherapy can achieve high rates of remission, even when monitored by the stringent PCR technique.

Publication types

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

MeSH terms

  • Adult
  • Aged
  • Agranulocytosis / chemically induced
  • Antineoplastic Combined Chemotherapy Protocols / adverse effects
  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use*
  • B-Lymphocytes / chemistry
  • Biomarkers, Tumor / blood*
  • Biomarkers, Tumor / genetics
  • Bleomycin / administration & dosage
  • Cisplatin / administration & dosage
  • Combined Modality Therapy
  • Cyclophosphamide / administration & dosage
  • Cytarabine / administration & dosage
  • Dexamethasone / administration & dosage
  • Doxorubicin / administration & dosage
  • Etoposide / administration & dosage
  • Female
  • Follow-Up Studies
  • Humans
  • Immunologic Factors / therapeutic use*
  • Interferon alpha-2
  • Interferon-alpha / therapeutic use*
  • Life Tables
  • Lymphoma, Non-Hodgkin / blood
  • Lymphoma, Non-Hodgkin / drug therapy*
  • Lymphoma, Non-Hodgkin / genetics
  • Lymphoma, Non-Hodgkin / mortality
  • Lymphoma, Non-Hodgkin / therapy
  • Male
  • Methylprednisolone / administration & dosage
  • Middle Aged
  • Mitoxantrone / administration & dosage
  • Neoplasm Staging
  • Oncogenes*
  • Polymerase Chain Reaction
  • Prednisone / administration & dosage
  • Procarbazine / administration & dosage
  • Proto-Oncogene Proteins / blood*
  • Proto-Oncogene Proteins / genetics
  • Proto-Oncogene Proteins c-bcl-2
  • Recombinant Proteins
  • Remission Induction
  • Treatment Outcome
  • Vincristine / administration & dosage

Substances

  • Biomarkers, Tumor
  • Immunologic Factors
  • Interferon alpha-2
  • Interferon-alpha
  • Proto-Oncogene Proteins
  • Proto-Oncogene Proteins c-bcl-2
  • Recombinant Proteins
  • Cytarabine
  • Bleomycin
  • Procarbazine
  • Vincristine
  • Etoposide
  • Dexamethasone
  • Doxorubicin
  • Cyclophosphamide
  • Mitoxantrone
  • Cisplatin
  • Prednisone
  • Methylprednisolone

Supplementary concepts

  • BACOD protocol
  • ESAP protocol
  • NOPP protocol