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GM-CSF can improve the cytogenetic response obtained with interferon-alpha therapy in patients with chronic myelogenous leukemia

  • ,
  • H. Kantarjian
    ,
  • S. O'Brien
    ,
  • R. Kurzrock
    ,
  • M. Keating
    ,
  • M. Talpaz(corresponding author)
*Corresponding author for this work
  • University of Texas Health Science Center at Houston
    ,
  • University of Texas MD Anderson Cancer Center
Scholary Output:
Contribution to journal
Article
Peer-review

Sustainable Development Goals

  • SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well

Abstract

Patients with chronic myelogenous leukemia (CML) who achieve a major cytogenetic remission when treated with interferon-α (IFN-A) have a survival advantage when compared to patients with no cytogenetic response. We investigated the effect of combining granulocyte-macrophage colony-stimulating factor (GM-CSF) with IFN-A in the cytogenetic response of patients with minor responses to IFN-A alone. CML patients were eligible if they had shown sensitivity to IFN-A as determined by achievement of a hematologic or cytogenetic response, but failed to achieve or lost a major cytogenetic response after a minimum of 12 months of therapy with IFN-A alone. Patients received GM-CSF 30 μg/m2 daily, subcutaneously and the dose was escalated to 60 μg/m2 if tolerated. IFN-A was continued at the same dose being received by the patient and escalated when possible. Fourteen evaluable patients were included, 13 in chronic phase and one in accelerated phase. The best response prior to GM-CSF was a transient major cytogenetic response in two patients (14%), minor cytogenetic response in nine (64%), and complete hematologic response in three (22%). The median time on IFN-A prior to the start of GM-CSF was 39 months (range 12-72 months). Four patients achieved a significant cytogenetic response, including two complete (14%) and two partial (14%) cytogenetic remissions during therapy. One partial cytogenetic remission converted to complete shortly after therapy was discontinued. Two other patients had a significant reduction in the percentage of Philadelphia chromosome-positive metaphases. The dose of IFN-A could be escalated in half of the patients treated. No toxicity could be attributed to the addition of GM-CSF. We conclude that the addition of GM-CSF to the treatment with IFN-A in CML patients who are sensitive to IFN-A alone but fail to achieve a major cytogenetic response may be beneficial in some patients and should be further investigated.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 860-864 (5 pages)

Journal (Volume, Issue Number)

Leukemia (Volume 12, Issue 6)

Publication milestones

  • Published - 1998

Publication status

Published - 1998

ISSN

0887-6924

Publication IDs

  • Scopus: 0031833734
  • PubMed: 9639411
  • ORCID: /0000-0002-8636-1071/work/68887939

Publication metrics

Metrics

SciVal
citations
49
Scopus
citations
SciVal
FWCI
1.24
SciVal
Author count
6
SciVal
Paper percentile
86
Fractional count
1
Fractional count
0.17
Fractional count
5
Fractional count
0.83
Fractional count
1
Fractional count
1

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Citation count
51
Captures
6