首页> 外文期刊>Blood: The Journal of the American Society of Hematology >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.
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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.

机译:达沙替尼140毫克一天一次的3期研究与对伊马替尼有加速期耐药或不耐受的慢性粒细胞白血病患者每天两次70毫克相比:中位随访15个月。

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摘要

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.
机译:达沙替尼是最有效的BCR-ABL抑制剂,在体外对未突变的BCR-ABL的效力比伊马替尼高325倍。研究表明,达沙替尼70 mg每天两次对不耐受或对伊马替尼耐药的加速期慢性髓性白血病患者具有益处。一项3期研究比较了每日一次140毫克达沙替尼与目前每日两次的疗效和安全性。在此,报告了加速期慢性粒细胞白血病(n = 317)亚组的结果,中位随访时间为15个月(治疗时间为0.03-31.15个月)。在随机接受每日一次(n = 158)或每天两次(n = 159)治疗的患者中,主要血液学和细胞遗传学应答率相当(主要血液学应答,66%vs 68%;主要细胞遗传学应答,39%vs。分别为43%)。估计的24个月无进展生存率分别为51%和55%,而总生存率则分别为63%和72%。每天一次的治疗与改善的安全性有关。尤其是,每天一次的组中出现胸腔积液的患者明显减少(所有级别,分别为20%和39%,P <.001)。这些结果表明,每天一次140毫克达沙替尼与每天两次70毫克达沙替尼具有相似的疗效,但安全性得到改善。该试验已在www.clinicaltrials.gov上注册为#CA180-035。

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