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吉西他滨与阿仑单抗联合新方案在高危复发/难治性慢性淋巴细胞白血病患者中的临床活性

Clinical activity of a new regimen combining gemcitabine and alemtuzumab in high-risk relapsed/refractory chronic lymphocytic leukemia patients.

作者信息

Oberic Lucie, Vaillant Willy, Hebraud Benjamin, Recher Christian, Suc Etienne, Houyau Philippe, Laurent Guy, Ysebaert Loic

机构信息

Department of Hematology, Purpan University Hospital, Toulouse cedex, France.

出版信息

Eur J Haematol. 2015 Jan;94(1):37-42. doi: 10.1111/ejh.12391. Epub 2014 Sep 17.

Abstract

Optimal treatment strategies are lacking in relapsed/refractory (R/R) chronic lymphocytic leukemia (CLL). Gemcitabine has shown activity and acceptable safety profile in B-cell lymphomas. We present a retrospective case review of gemcitabine and alemtuzumab, every 21 d (for up to six courses) in 27 community-based patients with high-risk R/R CLL. Median age was 70 yr (44-83 yr), 55% patients had Binet stage C, deletion 17p (del(17p)) and/or deletion 11q (del(11q)) were found in 65% and 27%, bulky disease in 55.5%, and fludarabine-refractoriness in 48% of cases, respectively. Overall response rate was 63% (29.6% clinical CR and 33.4% PR). At a median follow-up of 31 months, median PFS and OS were 15.4 and 24 months. In multivariate analysis, median OS is influenced by prior lines of treatment = 3 and bulky disease. Combination of alemtuzumab and gemcitabine appears to be an active, easy to administrate treatment in routine practice, high-risk R/R CLL patients.

摘要

复发/难治性(R/R)慢性淋巴细胞白血病(CLL)缺乏最佳治疗策略。吉西他滨在B细胞淋巴瘤中已显示出活性和可接受的安全性。我们对27例社区高危R/R CLL患者每21天(最多六个疗程)使用吉西他滨和阿仑单抗进行回顾性病例分析。中位年龄为70岁(44 - 83岁),55%的患者处于Binet分期C期,65%和27%的患者分别存在17号染色体短臂缺失(del(17p))和/或11号染色体长臂缺失(del(11q)),55.5%的患者有大包块疾病,48%的病例对氟达拉滨耐药。总缓解率为63%(29.6%为临床完全缓解,33.4%为部分缓解)。中位随访31个月时,中位无进展生存期(PFS)和总生存期(OS)分别为15.4个月和24个月。多因素分析显示,中位总生存期受既往治疗线数≥3和大包块疾病影响。在常规实践中,对于高危R/R CLL患者,阿仑单抗和吉西他滨联合似乎是一种有效的、易于给药的治疗方法。

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