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氟达拉滨、环磷酰胺和利妥昔单抗治疗慢性淋巴细胞白血病患者首次复发后的挽救治疗结果:法国协作组经验。

Salvage outcomes in patients with first relapse after fludarabine, cyclophosphamide, and rituximab for chronic lymphocytic leukemia: the French intergroup experience.

机构信息

Department of Hematology, Hôpitaux Universitaires De Strasbourg, Strasbourg, France.

Department of Hematology, Institut Paoli-Calmettes, Marseille, France.

出版信息

Am J Hematol. 2015 Jun;90(6):511-4. doi: 10.1002/ajh.23999. Epub 2015 Apr 1.

Abstract

The optimal management of patients with relapsed chronic lymphocytic leukemia (CLL) is dictated by the type of prior therapy, duration of prior response, presence of genomic aberrations, age, and comorbidities. The patterns of relapses and the clinical outcomes of second-line options after fludarabine-cyclophosphamide-rituximab (FCR) is given as a frontline treatment are currently unknown. In this retrospective and non-randomized study, we report the outcomes of 132 patients from databases of 14 French CLL study group centers who needed a second-line treatment after FCR frontline. Bendamustine + rituximab (BR) was the most frequently used second-line regimen, followed by alemtuzumab-based regimens, R-CHOP, and FCR. Median progression-free survival (PFS) was 18 months after BR with a median overall survival (OS) not reached. We also found that response durations of < 36 months and the presence of del(17p) are critical factors that contribute to poor overall survival. BR appears to be an effective salvage regimen in our series, both in terms of progression-free and overall survival. Patients who relapsed less than 36 months after FCR have a poor outcome, not significantly different in this study from patients with early relapses less than 12 or 24 months.

摘要

复发慢性淋巴细胞白血病(CLL)患者的最佳治疗方案取决于先前治疗的类型、先前缓解的持续时间、是否存在基因组异常、年龄和合并症。在氟达拉滨-环磷酰胺-利妥昔单抗(FCR)作为一线治疗后复发的模式和二线治疗的临床结果目前尚不清楚。在这项回顾性和非随机研究中,我们报告了来自 14 个法国 CLL 研究组中心数据库的 132 名患者的结果,这些患者在接受 FCR 一线治疗后需要二线治疗。苯达莫司汀联合利妥昔单抗(BR)是最常用的二线方案,其次是基于阿仑单抗的方案、R-CHOP 和 FCR。BR 后的中位无进展生存期(PFS)为 18 个月,中位总生存期(OS)未达到。我们还发现,<36 个月的缓解持续时间和 del(17p)的存在是导致总生存期不良的关键因素。在我们的研究中,BR 似乎是一种有效的挽救治疗方案,无论是在无进展生存期还是总生存期方面。在 FCR 后复发时间<36 个月的患者预后较差,与复发时间<12 个月或 24 个月的患者相比,在本研究中并无显著差异。

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