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首页> 外文期刊>AMERICAN JOURNAL OF HEMATOLOGY >Dasatinib 140 mg once daily versus 70 mg twice daily in patients with Ph-positive acute lymphoblastic leukemia who failed imatinib: Results from a phase 3 study†‡
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Dasatinib 140 mg once daily versus 70 mg twice daily in patients with Ph-positive acute lymphoblastic leukemia who failed imatinib: Results from a phase 3 study†‡

机译:伊马替尼治疗失败的Ph阳性急性淋巴细胞白血病患者,达沙替尼140毫克/天一次,每天70毫克; 3期研究的结果†

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摘要

Dasatinib 70 mg twice daily is indicated for Philadelphia chromosome-positive acute lymphoblastic leukemia (Ph+ ALL) intolerant or resistant to imatinib. In patients with chronic-phase chronic myelogenous leukemia, once-daily dosing has similar efficacy with improved safety, compared with twice-daily dosing. A phase 3 study (n = 611) assessed the efficacy and safety of dasatinib 140 mg once daily versus 70 mg twice-daily in patients with advanced phase chronic myelogenous leukemia or Ph+ ALL resistant or intolerant to imatinib. Here, results from the Ph+ ALL subset (n = 84) with a 2-year follow-up are reported. Patients were randomly assigned to receive dasatinib either 140 mg once daily (n = 40) or 70 mg twice daily (n = 44). The rate of confirmed major hematologic response with once-daily dosing (38%) was similar to that with twice-daily dosing (32%). The rate of major cytogenetic response with once-daily dosing (70%) was higher than that with twice-daily dosing (52%). Compared with the twice-daily schedule, the once-daily schedule had longer progression-free survival (median, 3.0 months versus 4.0 months, respectively) and shorter overall survival (median, 9.1 months versus 6.5 months, respectively). Overall safety profiles were similar between two groups, with nonhematologic adverse events being mostly grade 1 or 2. Pleural effusion was less frequent with once-daily dosing than with twice-daily dosing (all grades, 18% versus 32%). Notably, none of the differences between the two schedules was statistically significant. Compared with the 70 mg twice daily, dasatinib 140 mg once daily had similar overall efficacy and safety in patients with imatinib-resistant or intolerant Ph+ ALL. (clinicaltrials.gov identifier: NCT00123487). Am. J. Hematol. 2010. © 2009 Wiley-Liss, Inc.
机译:达沙替尼70 mg每天两次,用于不耐受或对伊马替尼耐药的费城染色体阳性急性淋巴细胞白血病(Ph + ALL)。在慢性阶段性慢性粒细胞性白血病患者中,与每天两次给药相比,每天一次给药具有相似的疗效和更高的安全性。一项3期研究(n = 611)评估了达沙替尼140 mg /天与每日两次70 mg /天对晚期慢性粒细胞性白血病或Ph + ALL耐药或不耐受伊马替尼的患者的疗效和安全性。在此,报告了Ph + ALL子集(n = 84)进行了2年随访的结果。患者被随机分配接受达沙替尼治疗,每日一次140 mg(n = 40)或每日两次70 mg(n = 44)。每日一次给药的确诊主要血液学应答率(38%)与每日两次给药的确证主要血液学应答率(32%)相似。每天一次给药的主要细胞遗传学应答率(70%)高于每天两次给药的主要细胞遗传学应答率(52%)。与每天两次的计划相比,每天一次的计划具有更长的无进展生存期(中位数分别为3.0个月和4.0个月)和较短的总体生存期(中位数分别为9.1个月和6.5个月)。两组之间的总体安全性状况相似,非血液学不良事件大多为1级或2级。每天一次给药的胸腔积液频率比每天两次给药的胸腔积液频率更低(所有级别,分别为18%和32%)。值得注意的是,两个时间表之间的差异均无统计学意义。与每日两次70毫克相比,达沙替尼140毫克每天一次对伊马替尼耐药或不耐受的Ph + ALL患者具有相似的总体疗效和安全性。 (clinicaltrials.gov标识符:NCT00123487)。上午。 J. Hematol。 2010。©2009 Wiley-Liss,Inc.。

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  • 来源
    《AMERICAN JOURNAL OF HEMATOLOGY》 |2010年第3期|p.164-170|共7页
  • 作者单位

    Chao Family Comprehensive Cancer Center, University of California, Irvine, Orange, California;

    Hematology and Oncology, Universitatsklinik Frankfurt, Frankfurt, Germany;

    San Francisco School of Medicine, University of California, San Francisco, California;

    University of Chicago Medical Center, Chicago, Illinois;

    CRLCC Institut Bergonié, Bordeaux, France;

    Medizinische Klinik, Universitatsklinikum Carl Gustav Carus Dresden, Dresden, Germany;

    III. Medizinische Klinik, Universittsmedizin Mannheim, Universitt Heidelberg, Mannheim, Germany;

    Institut Paoli Calmettes, Marseille, France;

    Department of Hematology, Hospital Britanico, Buenos Aires, Argentina;

    Department of Hematology, Hopital Saint Louis, Paris, France;

    Bristol-Myers Squibb, Wallingford, Connecticut;

    Bristol-Myers Squibb, Wallingford, Connecticut;

    Institute of Hematology and Medical Oncology, University of Bologna, Bologna, Italy;

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