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Prediction of initial cytogenetic response for subsequent major and complete cytogenetic response to imatinib mesylate therapy in patients with Philadelphia chromosome-positive chronic myelogenous leukemia

  • Hagop Kantarjian(corresponding author)
    ,
  • Moshe Talpaz
    ,
  • Susan O'Brien
    ,
  • Francis Giles
    ,
  • Mary Beth Rios
    ,
  • Kevin White
*Corresponding author for this work
  • 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

BACKGROUND. Obtaining a major (Philadelphia chromosome [Ph] of < 35%) or a complete cytogenetic response (Ph of 0%) has been associated with excellent long-term survival. Cytogenetic response may continue to improve with therapy. Because early allogeneic stem cell transplantation (SCT) may be associated with a better outcome, early parameters predicting for subsequent cytogenetic responses would optimize the treatment decision-making. METHODS. The current study was performed to analyze whether early cytogenetic responses may be predictive of later major or complete cytogenetic responses to imatinib mesylate therapy in patients with Ph-positive chronic myelogenous leukemia (CML). RESULTS. Two hundred sixty-one patients with Ph-positive, chronic-phase CML after failure with interferon therapy who were treated with imatinib mesylate therapy were analyzed. A persistence of 100% Ph-positive cells after ≥ 6 months of imatinib mesylate therapy was associated with a major cytogenetic response rate of 9-13% and a complete cytogenetic response rate of 0-4%. However, a minor cytogenetic response after 3-12 months of therapy still was associated with high rates of major (68-83%) or complete (35-54%) cytogenetic response rates. CONCLUSIONS. Patients with Ph-positive, chronic-phase CML who have persistent 100% Ph-positive disease after ≥ 6 months of imatinib mesylate therapy may be offered allogeneic SCT or considered for alternative investigational therapies.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 2225-2228 (4 pages)

Journal (Volume, Issue Number)

Cancer (Volume 97, Issue 9)

Publication milestones

  • Published - 05/01/2003

Publication status

Published - 05/01/2003

ISSN

0008-543X

Publication IDs

  • Scopus: 19244365122
  • PubMed: 12712475
  • ORCID: /0000-0002-8636-1071/work/68811081

Publication metrics

Metrics

SciVal
citations
22
Scopus
citations
SciVal
FWCI
1.20
SciVal
Author count
12
SciVal
Paper percentile
72
Fractional count
1
Fractional count
0.08
Fractional count
11
Fractional count
0.92
Fractional count
1
Fractional count
1

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Captures
20
Citation count
24