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Ibrutinib as a salvage therapy after allogeneic HCT for chronic lymphocytic leukemia

机译:Ibrutinib作为同种异体HCT慢性淋巴细胞白血病后的救生疗法

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The purpose of our study is to provide information on safety and efficacy of ibrutinib as salvage treatment after allo-HSCT for CLL. A total of 56 patients were included, 36 (64%) males; median age at transplantation was 48 years (range: 35-64) and the median number of treatment lines prior to transplantation was 3 (1-10). The median time between allo-HSCT and Ibrutinib was 30 months (range: 1-140). Overall, 40 (71%) patients responded to Ibrutinib; 23 (41%) PR, and 17 (30%) CR. At time of ibrutinib initiation, ten patients had active chronic GVHD that resolved under Ibrutinib, whilst a single patient developed limited de novo chronic GVHD on Ibrutinib. Fourteen patients discontinued ibrutinib, four because of toxicity and ten because of disease progression. Overall, 14 patients progressed (median PFS = 24 months) among them 10 died. Two-year OS and PFS probabilities were 72% (95% CI: 52-84) and 50% (95% CI: 32-66), respectively. Patients with late relapse after allo-HSCT (>= 24 months) had a better PFS after ibrutinib. Our study shows that ibrutinib can be safely administered for CLL relapse after allo-HSCT, with comparable efficacy to non-transplanted patients with high-risk disease.
机译:我们研究的目的是提供有关伊布洛替尼的安全性和疗效的信息,作为CLL的Allo-HSCT后的抢救治疗。共有56名患者,36例(64%)男性;移植的中位年龄为48岁(范围:35-64),移植前的治疗管数量为3(1-10)。 Allo-Hsct和Ibrutinib之间的中位时间为30个月(范围:1-140)。总体而言,40名(71%)患者对Ibrutinib的反应; 23(41%)Pr,17(30%)Cr。在Ibrutinib启动的时候,十名患者有活跃的慢性GVHD,在伊布勒替尼下解决,而单身患者在Ibrutinib上发育了有限的De Novo慢性GVHD。十四名患者停产伊布鲁替尼,由于毒性和疾病进展而死。总体而言,14名患者进展(中位数PFS = 24个月)在10中死亡。两年的OS和PFS概率分别为72%(95%CI:52-84)和50%(95%CI:32-66)。在伊布洛尼布后allo-hsct(> = 24个月)后复发后患者有更好的PFS。我们的研究表明,伊布洛替尼可以安全地施用Allo-HSCT后的ClL复发,对未移植的高风险疾病的患者具有相当的疗效。

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