Yang F, Cai W Z, Huang X W, Xue S L, Fu C C, Tang X W, Sun A N, Wu D P, Qiu H Y
Jiangsu Institute of Hematology, the First Affiliated Hospital of Soochow University, Key Laboratory of Thrombosis and Hemostasis of Ministry of Health, Jiangsu Clinical Medicine Center, Suzhou 215006, China.
Zhonghua Xue Ye Xue Za Zhi. 2018 Aug 14;39(8):661-667. doi: 10.3760/cma.j.issn.0253-2727.2018.08.010.
To investigate the efficacy of first-line administration of generic dasatinib or first-generation TKI (imatinib) in patients with Philadelphia chromosome positive acute lymphoblastic leukemia (Ph(+) ALL) treated by hematopoietic stem cell transplantation (HSCT). Clinical features and prognoses of 63 newly diagnosed Ph(+) ALL patients from Jan 2014 to June 2017 treated by HSCT combined with first-line administration of generic dasatinib or imatinib were retrospective analyzed. Of 63 Ph(+) ALL patients, 31 cases were administered generic dasatinib, and the other 32 ones imatinib. Complete remission (CR) rates at the fourth week of induction therapy in generic dasatinib and imatinib groups were 96.8% and 93.8% (=1.000) , respectively. Meanwhile major molecular response (MMR; BCR-ABL/ABL reduce 3log) rates were 41.9% and 43.8% ((2)=0.021, =0.884), respectively. Relapse rates before transplantation were 6.5% and 12.5% (=0.672), respectively. MMR rates before HSCT were 83.9% and 68.8% ((2)=1.985, =0.159), respectively. The 20-monthes overall survival (OS) rates of generic dasatinib and imatinib groups were 95.5% and 76.5% ((2)=0.990, =0.320) respectively; 20-monthes event-free survival (EFS) rates were 93.5% and 61.4% ((2)=5.926, =0.015), respectively. Statistically significant differences of EFS were reached. Multiple factors analysis showed that generic dasatinib (=0.201, 95% 0.045-0.896, =0.035) and MMR before transplantation (=0.344, 95% 0.124-0.956, =0.041) could improve EFS. First-line administration of generic dasatinib could improve EFS for Ph(+)ALL patients treated by HSCT when compered with imatinib.
探讨在接受造血干细胞移植(HSCT)治疗的费城染色体阳性急性淋巴细胞白血病(Ph(+)ALL)患者中,一线使用通用型达沙替尼或第一代酪氨酸激酶抑制剂(TKI,伊马替尼)的疗效。对2014年1月至2017年6月期间63例新诊断的接受HSCT联合一线通用型达沙替尼或伊马替尼治疗的Ph(+)ALL患者的临床特征和预后进行回顾性分析。63例Ph(+)ALL患者中,31例接受通用型达沙替尼治疗,另外32例接受伊马替尼治疗。通用型达沙替尼组和伊马替尼组诱导治疗第4周时的完全缓解(CR)率分别为96.8%和93.8%(P=1.000)。同时,主要分子反应(MMR;BCR-ABL/ABL降低3log)率分别为41.9%和43.8%(P=0.021,P=0.884)。移植前复发率分别为6.5%和12.5%(P=0.672)。HSCT前MMR率分别为83.9%和68.8%(P=1.985,P=0.159)。通用型达沙替尼组和伊马替尼组的20个月总生存(OS)率分别为95.5%和76.5%(P=0.990,P=0.320);20个月无事件生存(EFS)率分别为93.5%和61.4%(P=5.926,P=0.015)。EFS有统计学显著差异。多因素分析显示通用型达沙替尼(P=0.201,95%CI 0.045-0.896,P=0.035)和移植前MMR(P=0.344,95%CI 0.124-0.956,P=0.041)可改善EFS。与伊马替尼相比,一线使用通用型达沙替尼可改善接受HSCT治疗的Ph(+)ALL患者的EFS。