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Evaluation of cardiovascular ischemic event rates in dasatinib-treated patients using standardized incidence ratios

  • Giuseppe Saglio(corresponding author)
    ,
  • Philipp le Coutre
    ,
  • ,
  • Jiří Mayer
    ,
  • Philip Rowlings
    ,
  • François Xavier Mahon
*Corresponding author for this work
  • University of Turin
    ,
  • Charité – Universitätsmedizin Berlin
    ,
  • University of Texas MD Anderson Cancer Center
    ,
  • Masaryk University
    ,
  • University of Newcastle
    ,
  • CHU de Bordeaux
Scholary Output:
Contribution to journal
Article
Peer-review

Open access

Sustainable Development Goals

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

Abstract

With high survival rates for chronic myeloid leukemia (CML) patients treated with BCR-ABL1 tyrosine kinase inhibitors (TKIs), emerging consequences, such as arterial ischemic events, require consideration when evaluating treatment options. Cardiovascular ischemic event incidence in clinical trials was evaluated in 2712 dasatinib-treated patients with Philadelphia chromosome-positive (Ph+) leukemias from 11 first- and second-line trials (pooled), newly diagnosed CML patients treated with dasatinib or imatinib (DASISION), and prostate cancer patients treated with dasatinib or placebo plus docetaxel/prednisone (READY). Overall, 2–4% of dasatinib-treated patients had cardiovascular ischemic events. Most dasatinib-treated patients with an event had a history of and/or risk factor for atherosclerosis (pooled 77 with history/risk and event/96 with events; DASISION 8/10; READY 15/18). Most cardiovascular ischemic events occurred within 1 year of initiating dasatinib (pooled 69/96; DASISION 7/10; READY 16/18). Comparison of observed and expected event rates through standardized incidence ratios indicates that dasatinib does not increase risk for cardiovascular ischemic events compared with external reference populations.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 1303-1313 (11 pages)

Journal (Volume, Issue Number)

Annals of Hematology (Volume 96, Issue 8)

Publication milestones

  • Published - 08/01/2017

Publication status

Published - 08/01/2017

ISSN

0939-5555

Publication IDs

  • Scopus: 85019959948
  • PubMed: 28534184
  • ORCID: /0000-0002-8636-1071/work/68810938

Publication metrics

Metrics

SciVal
FWCI
0.83
SciVal
Author count
10
SciVal
citations
12
SciVal
Paper percentile
79
Fractional count
1
Fractional count
0.10
Fractional count
9
Fractional count
0.90
Fractional count
1
Fractional count
1
Scopus
citations

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Captures
44
Citation count
17

Funding Details

The authors thank the participating patients and families for making these Bristol-Myers Squibb–sponsored trials possible. This analysis was supported by funding from Bristol-Myers Squibb. Professional medical writing and editorial assistance was provided by Samantha L. Dwyer, PhD, and Kelly M. Fahrbach, PhD, at StemScientific, an Ashfield Company, part of UDG Healthcare plc, and was funded by Bristol-Myers Squibb.