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首页> 外文期刊>Blood: The Journal of the American Society of Hematology >Randomized study of reduced-intensity chemotherapy combined with imatinib in adults with Ph-positive acute lymphoblastic leukemia
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Randomized study of reduced-intensity chemotherapy combined with imatinib in adults with Ph-positive acute lymphoblastic leukemia

机译:成人Ph阳性急性淋巴细胞白血病减强度化疗联合伊马替尼的随机研究

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In this study, we randomly compared high doses of the tyrosine kinase inhibitor imatinib combined with reduced-intensity chemotherapy (arm A) to standard imatinib/hyperCVAD (cyclophosphamide/vincristine/doxorubicin/dexamethasone) therapy (arm B) in 268 adults (median age, 47 years) with Philadelphia chromosome-positive (Ph+) acute lymphoblastic leukemia (ALL). The primary objective was the major molecular response (MMolR) rate after cycle 2, patients being then eligible for allogeneic stem cell transplantation (SCT) if they had a donor, or autologous SCT if in MMolR and no donor. With fewer induction deaths, the complete remission (CR) rate was higher in arm A than in arm B (98% vs 91%; P=.006), whereas the MMolR rate was similar in both arms (66% vs 64%). With a median follow-up of 4.8 years, 5-year event-free survival and overall survival (OS) rates were estimated at 37.1% and 45.6%, respectively, without difference between the arms. Allogeneic transplantation was associated with a significant benefit in relapse-free survival (hazard ratio [HR], 0.69; P =.036) and OS (HR, 0.64; P =.02), with initial white blood cell count being the only factor significantly interacting with this SCT effect. In patients achieving MMolR, outcome was similar after autologous and allogeneic transplantation. This study validates an induction regimen combining reduced-intensity chemotherapy and imatinib in Ph+ ALL adult patients and suggests that SCT in first CR is still a good option for Ph+ALL adult patients. This trial was registered at www.clinicaltrials.govas # NCT00327678.
机译:在这项研究中,我们在268名成人(中位年龄)中随机比较了大剂量的酪氨酸激酶抑制剂伊马替尼联合降低强度的化疗(A组)与标准伊马替尼/ hyperCVAD(环磷酰胺/长春新碱/阿霉素/地塞米松)治疗(B组) (47岁),费城染色体阳性(Ph +)急性淋巴细胞白血病(ALL)。主要目标是第2周期后的主要分子应答(MMolR)率,如果患者有供体,则有资格进行同种异体干细胞移植(SCT);如果在MMolR中且无供体,则有自体SCT。随着诱导死亡的减少,A组的完全缓解(CR)率高于B组(98%vs 91%; P = .006),而两个组的MMolR率相似(66%vs 64%) 。中位随访时间为4.8年,估计5年无事件生存率和总生存率分别为37.1%和45.6%,两组之间无差异。同种异体移植与无复发生存(危险比[HR],0.69; P = .036)和OS(HR,0.64; P = .02)有显着的相关性,而初始白细胞计数是唯一因素与此SCT效应有很大的相互作用。自体和同种异体移植后,达到MMolR的患者的预后相似。这项研究验证了在Ph + ALL成年患者中结合降低强度化学疗法和伊马替尼的诱导方案,并提示对于CR + ALL成年患者而言,首次CR的SCT仍然是一个不错的选择。该试验已在www.clinicaltrials.govas上注册,编号为NCT00327678。

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