Takahashi Koichi, Kantarjian Hagop M, Yang Yulong, Sasaki Koji, Jain Preetesh, DellaSala Sara, Ravandi Farhad, Kadia Tapan, Pemmaraju Naveen, Daver Naval, Borthakur Gautam, Garcia-Manero Guillermo, Jabbour Elias, Cortes Jorge E
Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Department of Genomic Medicine, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Cancer. 2016 Nov 15;122(21):3336-3343. doi: 10.1002/cncr.30197. Epub 2016 Aug 10.
Both dasatinib and nilotinib are approved frontline therapy for chronic myeloid leukemia in chronic phase (CML-CP) based on randomized trials compared with imatinib. However, no head-to-head comparison of dasatinib and nilotinib has been conducted in patients with newly diagnosed CML-CP.
The authors conducted a propensity score (PS) matched comparison of patients with CML-CP who received frontline therapy with either dasatinib (N = 102) or nilotinib (N = 104) under the respective phase 2 trials conducted in parallel.
PS matching resulted in 87 patients from each trial being matched for pretreatment characteristics. The 3-month BCR-ABL1/ABL1 ratio <10% rate was 93% with dasatinib and 94% with nilotinib (P = .25); the rates of major molecular response at 12 months were 77% and 85%, respectively (P = .13); and the rates of molecular response with 4.5-log reduction in the ratio at 36 months were 66% and 64%, respectively (P = .96). All other clinically relevant responses were similar between the 2 treatment cohorts. The 3-year probability of event-free survival was 89% among the patients who received dasatinib and 87% among those who received nilotinib (P = .99), and the corresponding 3-year overall survival probabilities were 99% and 93%, respectively (P = .95). No statistical difference was observed between the dasatinib and nilotinib groups in any of the other survival endpoints. The treatment discontinuation rate also was similar between the 2 cohorts (dasatinib group, 18%; nilotinib group, 19%; P = .82).
In a PS-matched cohort of patients with newly diagnosed CML-CP, dasatinib and nilotinib offer similar response and survival outcomes. Both drugs can be considered reasonable standard-of-care options as first-line therapy for patients with CML-CP. Cancer 2016;122:3336-3343. © 2016 American Cancer Society.
基于与伊马替尼对比的随机试验,达沙替尼和尼洛替尼均被批准作为慢性期慢性髓性白血病(CML-CP)的一线治疗药物。然而,尚未在新诊断的CML-CP患者中对达沙替尼和尼洛替尼进行直接对比。
作者在平行开展的各自2期试验中,对接受一线治疗的CML-CP患者进行了倾向评分(PS)匹配对比,其中接受达沙替尼治疗的患者有102例,接受尼洛替尼治疗的患者有104例。
PS匹配后,每个试验各有87例患者的预处理特征相匹配。达沙替尼组3个月时BCR-ABL1/ABL1比率<10%的比例为93%,尼洛替尼组为94%(P = 0.25);12个月时主要分子反应率分别为77%和85%(P = 0.13);36个月时比率降低4.5个对数的分子反应率分别为66%和64%(P = 0.96)。两个治疗队列之间所有其他临床相关反应相似。接受达沙替尼治疗的患者3年无事件生存率为89%,接受尼洛替尼治疗的患者为87%(P = 0.99),相应的3年总生存率分别为99%和93%(P = 0.95)。在任何其他生存终点方面,达沙替尼组和尼洛替尼组之间均未观察到统计学差异。两个队列的治疗中断率也相似(达沙替尼组为18%;尼洛替尼组为19%;P = 0.82)。
在PS匹配的新诊断CML-CP患者队列中,达沙替尼和尼洛替尼的反应和生存结果相似。两种药物均可被视为CML-CP患者一线治疗合理的标准治疗选择。《癌症》2016年;122:3336 - 3343。©2016美国癌症协会。