Chao Family Comprehensive Cancer Center, University of California, Irvine, Orange, USA.
Am J Hematol. 2010 Mar;85(3):164-70. doi: 10.1002/ajh.21615.
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).
达沙替尼每天两次 70mg 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)。在慢性期慢性髓性白血病患者中,与每天两次相比,每日一次剂量具有相似的疗效且安全性提高。一项 3 期研究(n=611)评估了达沙替尼每天一次 140mg 与每天两次 70mg 用于对伊马替尼耐药或不耐受的晚期慢性髓性白血病或 Ph+ALL 患者的疗效和安全性。在此,报道了具有 2 年随访的 Ph+ALL 亚组(n=84)的结果。患者随机接受达沙替尼每天一次 140mg(n=40)或每天两次 70mg(n=44)。每天一次剂量组的确认主要血液学缓解率(38%)与每天两次剂量组相似(32%)。每天一次剂量组的主要细胞遗传学缓解率(70%)高于每天两次剂量组(52%)。与每天两次剂量相比,每天一次剂量的无进展生存期更长(中位数分别为 3.0 个月和 4.0 个月),总生存期更短(中位数分别为 9.1 个月和 6.5 个月)。两组的总体安全性相似,非血液学不良事件主要为 1 级或 2 级。与每天两次剂量相比,胸腔积液的发生频率较低(所有级别,18%与 32%)。值得注意的是,两种方案之间的差异均无统计学意义。与每天两次 70mg 相比,达沙替尼每天一次 140mg 在对伊马替尼耐药或不耐受的 Ph+ALL 患者中具有相似的总体疗效和安全性。(临床试验.gov 标识符:NCT00123487)。