首页> 美国卫生研究院文献>Haematologica >The response to imatinib and interferon-α is more rapid than the response to imatinib alone: a retrospective analysis of 495 Philadelphia-positive chronic myeloid leukemia patients in early chronic phase
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The response to imatinib and interferon-α is more rapid than the response to imatinib alone: a retrospective analysis of 495 Philadelphia-positive chronic myeloid leukemia patients in early chronic phase

机译:对伊马替尼和干扰素-α的反应比对伊马替尼的反应更快:回顾性分析了495例费城阳性慢性髓性白血病早期慢性期患者

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摘要

Before the introduction of imatinib, interferon α-based regimens were the gold standard for treatment of early chronic phase chronic myeloid leukemia patients. The combination of IFN-α with imatinib is currently being investigated in at least two large clinical trials, the German CML Study IV and the French SPIRIT trial.We reviewed the cytogenetic and molecular responses of 76 early chronic phase chronic myeloid leukemia patients who were treated with imatinib and interferon-α and of 419 early chronic phase chronic myeloid leukemia patients treated with imatinib alone front-line.The complete cytogenetic response rate was higher in the IM+IFN-α group than in the imatinib group at six months (60% vs. 42%; P=0.003), but not at 48 months (88% vs. 88%). The durability of the complete cytogenetic response was similar in the two groups with 94% and 91% of complete cytogenetic responders in continuous complete cytogenetic response at 48 months (P=0.56). The major molecular response rate was higher in the IM+IFN-α group at six months (58% vs. 34%; P=0.0001) and 12 months (67% vs. 47%; P=0.001) but not later on (65% vs. 57% at 48 months; P=0.25). Overall and progression free survival were comparable in the two groups; a significant trend to a better event free survival was observed in patients treated with PegIFNα (91% vs. 78%; P=0.02).These data suggest that the response to the combination treatment is more rapid. It is not yet known how much a rapid reduction will influence the longer-term overall and progression free survival, and the cure rate.
机译:在引入伊马替尼之前,基于干扰素α的治疗方案是治疗早期慢性期慢性粒细胞白血病患者的金标准。目前正在至少两项大型临床试验(德国CML研究IV和法国SPIRIT试验)中研究IFN-α与伊马替尼的联合用药。我们回顾了76例接受治疗的早期慢性慢性粒细胞白血病患者的细胞遗传学和分子反应单独使用伊马替尼一线治疗的419名早期慢性阶段慢性粒细胞白血病患者接受伊马替尼和干扰素-α治疗.IM +IFN-α组在六个月时的完全细胞遗传学应答率高于伊马替尼组(60% vs. 42%; P = 0.003),但在48个月时没有(88%vs. 88%)。两组的完全细胞遗传学应答的持久性相似,分别在48个月的连续完全细胞遗传学应答中分别有94%和91%的完全细胞遗传学应答者(P = 0.56)。 IM +IFN-α组的主要分子应答率在六个月(58%比34%; P = 0.0001)和12个月(67%比47%; P = 0.001)更高,但在随后的几个月( 65%比48个月时的57%; P = 0.25)。两组的总体生存率和无进展生存率相当。在接受PegIFNα治疗的患者中观察到无事件存活率更高的显着趋势(91%vs. 78%; P = 0.02)。这些数据表明,对联合治疗的反应更快。尚不知道快速减少将对长期总体生存和无进展生存率以及治愈率产生多少影响。

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