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Phase 3 study of dasatinib 140 mg once daily versus 70 mg twice daily in patients with chronic myeloid leukemia in accelerated phase resistant or intolerant to imatinib: 15-Month median follow-up

  • Hagop Kantarjian(corresponding author)
    ,
  • ,
  • Dong Wook Kim
    ,
  • Pedro Dorlhiac-Llacer
    ,
  • Ricardo Pasquini
    ,
  • John DiPersio
*Corresponding author for this work
  • University of Texas Health Science Center at Houston
    ,
  • The Catholic University of Korea
    ,
  • Universidade de São Paulo
    ,
  • Universidade Federal do Paraná
    ,
  • Washington University St. Louis
    ,
  • Heidelberg University 
Scholary Output:
Contribution to journal
Article
Peer-review

Open access

Abstract

Dasatinib is the most potent BCR-ABL inhibitor, with 325-fold higher potency than imatinib against unmutated BCR-ABL in vitro. Studies have demonstrated the benefits of dasatinib 70 mg twice daily in patients with accelerated-phase chronic myeloid leukemia intolerant or resistant to imatinib. A phase 3 study compared the efficacy and safety of dasatinib 140 mg once daily with the current twice-daily regimen. Here, results from the subgroup with accelerated-phase chronic myeloid leukemia (n = 317) with a median follow-up of 15 months (treatment duration, 0.03-31.15 months) are reported. Among patients randomized to once-daily (n = 158) or twice-daily (n = 159) treatment, rates of major hematologic and cytogenetic responses were comparable (major hematologic response, 66% vs 68%; major cytogenetic response, 39% vs 43%, respectively). Estimated progression-free survival rates at 24 months were 51% and 55%, whereas overall survival rates were 63% versus 72%. Once-daily treatment was associated with an improved safety profile. In particular, significantly fewer patients in the once-daily group experienced a pleural effusion (all grades, 20% vs 39% P < .001). These results demonstrate that dasatinib 140 mg once daily has similar efficacy to dasatinib 70 mg twice daily but with an improved safety profile. This trial is registered at www.clinicaltrials.gov as #CA180-035.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 6322-6329 (8 pages)

Journal (Volume, Issue Number)

Blood (Volume 113, Issue 25)

Publication milestones

  • Published - 2009

Publication status

Published - 2009

ISSN

0006-4971

Publication IDs

  • Scopus: 67650607999
  • PubMed: 19369231
  • ORCID: /0000-0002-8636-1071/work/68811189

Publication metrics

Metrics

SciVal
citations
141
Fractional count
1
Fractional count
0.08
Fractional count
12
Fractional count
0.92
Fractional count
1
Fractional count
1
Scopus
citations
SciVal
FWCI
5.48
SciVal
Author count
13
SciVal
Paper percentile
97
SciVal
Top percentile
5

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Citation count
166
Captures
98

Funding Details

FunderFunding number
NCI
P30CA016672