Results of therapy with interferon alpha and cyclic combination chemotherapy in patients with philadelphia chromosome positive chronic myelogenous leukemia in early chronic phase

Leuk Lymphoma. 2001 Apr;41(3-4):309-19. doi: 10.3109/10428190109057985.

Abstract

The objective of the study was to investigate the toxicity and efficacy of cyclic combination therapy offered to patients with Ph-positive CML having a sub-optimal response to IFN-alpha. Patients in early chronic phase CML were treated with IFN-alpha at 5MU/m(2) daily. Patients who did not achieve cytogenetic response after 6 months of IFN-alpha therapy, or Ph-suppression to less than 35% Ph-positive cells (partial cytogenetic response) after 12 months of therapy were offered cyclic intensive chemotherapy every 6 months, with IFN-alpha maintenance between cycles. The initial 3 cycles included daunorubicin, vincristine, cytosine arabinoside (ara-C) and prednisone (DOAP). Later cycles were given with cyclophosphamide replacing daunorubicin (COAP). Of 74 patients treated, 61 (82%) achieved complete hematologic response (CHR): 51 (69%) had a cytogenetic response, which was major (Ph < 35%) in 31 (42%), and complete in 23 (31%). Fifty-five patients (74%) achieved CHR by 6 months of therapy, 38 (69%; 51% of total) with a cytogenetic response - 13 (24%) had a major cytogenetic response. Seventeen patients received at least 1 course of DOAP therapy. Median survival of the overall cohort of patients was 120 months. With a median follow-up of 145 months (103+ to 155+ months), 40 patients (54%) have died. The median duration of cytogenetic response was 35 months (range 3 to 149+ months) and the estimated 10-year cytogenetic response rate was 37%. A durable complete cytogenetic response was observed in 16 patients (20%) with a median duration of 139+ months (range 12+ to 149+ months), 11 of them (15%) are now off IFN-alpha therapy for a median of 57+ months (range 12+ to 128+ months). The projected 10-year survival was 50% for the study group versus 35% for 208 patients who received other IFN-alpha based regimens at the MD Anderson Cancer Center (p<.01). In conclusion, the addition of intensive chemotherapy may improve survival in patients with CML who have not obtained an adequate cytogenetic response on an IFN-alpha-based regimen.

Publication types

  • Clinical Trial

MeSH terms

  • Actuarial Analysis
  • Adolescent
  • Adult
  • Aged
  • Antineoplastic Combined Chemotherapy Protocols / administration & dosage
  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use*
  • Antineoplastic Combined Chemotherapy Protocols / toxicity
  • Cohort Studies
  • Cyclophosphamide / administration & dosage
  • Cyclophosphamide / toxicity
  • Cytarabine / administration & dosage
  • Cytarabine / toxicity
  • Cytogenetic Analysis
  • Daunorubicin / administration & dosage
  • Daunorubicin / toxicity
  • Disease-Free Survival
  • Drug Administration Schedule
  • Female
  • Humans
  • Interferon-alpha / administration & dosage*
  • Interferon-alpha / toxicity
  • Leukemia, Myelogenous, Chronic, BCR-ABL Positive / complications
  • Leukemia, Myelogenous, Chronic, BCR-ABL Positive / drug therapy*
  • Leukemia, Myelogenous, Chronic, BCR-ABL Positive / mortality
  • Leukemia, Myeloid, Chronic-Phase / complications
  • Leukemia, Myeloid, Chronic-Phase / drug therapy
  • Leukemia, Myeloid, Chronic-Phase / mortality
  • Male
  • Middle Aged
  • Prednisolone / administration & dosage
  • Prednisolone / toxicity
  • Prednisone / administration & dosage
  • Prednisone / toxicity
  • Risk Factors
  • Survival Rate
  • Therapeutic Equivalency
  • Treatment Outcome
  • Vincristine / administration & dosage
  • Vincristine / toxicity

Substances

  • Interferon-alpha
  • Cytarabine
  • Vincristine
  • Cyclophosphamide
  • Prednisolone
  • Prednisone
  • Daunorubicin

Supplementary concepts

  • COAP protocol
  • CROP protocol