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初治 CLL 患者中 FCR 联合或不联合米托蒽醌的随机 IIB 期 ADMIRE 试验结果。

Results of the randomized phase IIB ADMIRE trial of FCR with or without mitoxantrone in previously untreated CLL.

机构信息

Department of Haematology, St James's University Hospital, Leeds, UK.

Clinical Trials Research Unit, Leeds Institute of Clinical Trials Research, University of Leeds, Leeds, UK.

出版信息

Leukemia. 2017 Oct;31(10):2085-2093. doi: 10.1038/leu.2017.65. Epub 2017 Apr 20.

Abstract

ADMIRE was a multicenter, randomized-controlled, open, phase IIB superiority trial in previously untreated chronic lymphocytic leukemia. Conventional front-line therapy in fit patients is fludarabine, cyclophosphamide and rituximab (FCR). Initial evidence from non-randomized phase II trials suggested that the addition of mitoxantrone to FCR (FCM-R) improved remission rates. Two hundred and fifteen patients were recruited to assess the primary end point of complete remission (CR) rates according to International Workshop on Chronic Lymphocytic Leukemia criteria. Secondary end points were progression-free survival (PFS), overall survival (OS), overall response rate, minimal residual disease (MRD) negativity and safety. At final analysis, CR rates were 69.8 FCR vs 69.3% FCM-R (adjusted odds ratio (OR): 0.97; 95% confidence interval (CI): (0.53-1.79), P=0.932). MRD-negativity rates were 59.3 FCR vs 50.5% FCM-R (adjusted OR: 0.70; 95% CI: (0.39-1.26), P=0.231). During treatment, 60.0% (n=129) of participants received granulocyte colony-stimulating factor as secondary prophylaxis for neutropenia, a lower proportion on FCR compared with FCM-R (56.1 vs 63.9%). The toxicity of both regimens was acceptable. There are no significant differences between the treatment groups for PFS and OS. The trial demonstrated that the addition of mitoxantrone to FCR did not increase the depth of response. Oral FCR was well tolerated and resulted in impressive responses in terms of CR rates and MRD negativity compared with historical series with intravenous chemotherapy.

摘要

ADMIRE 是一项多中心、随机对照、开放、IIB 期优效性试验,纳入了未经治疗的慢性淋巴细胞白血病患者。适合的患者的传统一线治疗是氟达拉滨、环磷酰胺和利妥昔单抗(FCR)。来自非随机 II 期试验的初步证据表明,米托蒽醌联合 FCR(FCM-R)可提高缓解率。招募了 215 名患者,根据国际慢性淋巴细胞白血病工作组标准评估完全缓解(CR)率这一主要终点。次要终点包括无进展生存期(PFS)、总生存期(OS)、总缓解率、微小残留病(MRD)阴性率和安全性。最终分析显示,CR 率在 FCR 组为 69.8%,FCM-R 组为 69.3%(调整后的优势比(OR):0.97;95%置信区间(CI):(0.53-1.79),P=0.932)。MRD 阴性率在 FCR 组为 59.3%,FCM-R 组为 50.5%(调整后的 OR:0.70;95% CI:(0.39-1.26),P=0.231)。在治疗期间,60.0%(n=129)的参与者接受了粒细胞集落刺激因子作为中性粒细胞减少症的二级预防,FCR 组的比例低于 FCM-R 组(56.1% vs 63.9%)。两种方案的毒性均可接受。两组之间的 PFS 和 OS 无显著差异。该试验表明,米托蒽醌联合 FCR 并未增加缓解深度。与静脉化疗的历史系列相比,口服 FCR 的耐受性良好,在 CR 率和 MRD 阴性率方面产生了令人印象深刻的反应。

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