Suppr超能文献

MURANO研究:复发/难治性慢性淋巴细胞白血病患者接受维奈托克联合利妥昔单抗治疗的最终分析及再治疗/交叉亚研究结果

The MURANO study: final analysis and retreatment/crossover substudy results of VenR for patients with relapsed/refractory CLL.

作者信息

Kater Arnon P, Harrup Rosemary, Kipps Thomas J, Eichhorst Barbara, Owen Carolyn J, Assouline Sarit, Lamanna Nicole, Robak Tadeusz, de la Serna Javier, Jaeger Ulrich, Cartron Guillaume, Montillo Marco, Mellink Clemens, Langerak Anton W, Chyla Brenda, Popovic Relja, Jiang Yanwen, Millen Rosemary, Lefebure Marcus, Thadani-Mulero Maria, Boyer Michelle, Seymour John F

机构信息

Department of Hematology, Cancer Center Amsterdam, Amsterdam University Medical Centers, Amsterdam, The Netherlands.

Department of Cancer and Blood Services, Royal Hobart Hospital and University of Tasmania, Hobart, TAS, Australia.

出版信息

Blood. 2025 Jun 5;145(23):2733-2745. doi: 10.1182/blood.2024025525.

Abstract

Fixed-duration venetoclax-rituximab (VenR) in patients with relapsed/refractory chronic lymphocytic leukemia (CLL) in the phase 3 MURANO trial resulted in superior progression-free survival (PFS) and overall survival (OS) vs bendamustine-rituximab (BR). We report the final analyses of MURANO (median follow-up, 7 years). Patients were randomized to VenR (venetoclax 400 mg daily for 2 years plus monthly rituximab for 6 months; n = 194) or BR (6 months; n = 195). In a substudy, patients with progressive disease (PD) received VenR as retreatment or crossover from BR. At the final data cut (3 August 2022), the median PFS with VenR was 54.7 months vs 17.0 months with BR. The 7-year PFS with VenR was 23.0%. The 7-year OS was 69.6% and 51.0%, respectively. Among VenR-treated patients with undetectable minimal residual disease (MRD; uMRD) and no PD at end of treatment (EOT; n = 83), the median PFS from EOT was 52.5 vs 18.0 months in patients with MRD at EOT (n = 35; P < .0001). Fourteen patients had enduring uMRD. Three distinct mutations in BCL2 in 4 patients were identified. In the substudy, 25 patients were retreated with VenR, and 9 patients crossed over to VenR; the median PFS was 23 and 27 months, and the best overall response rate was 72% and 89%, respectively. At the end of combination treatment (EOCT), after retreatment or crossover, 8 and 6 patients achieved uMRD, respectively. No new safety findings were observed. Overall, these final MURANO analyses support consideration of fixed-duration VenR therapy for patients with relapsed/refractory CLL. This trial was registered at www.clinicaltrials.gov as #NCT02005471.

摘要

在3期MURANO试验中,复发/难治性慢性淋巴细胞白血病(CLL)患者接受固定疗程的维奈克拉-利妥昔单抗(VenR)治疗,与苯达莫司汀-利妥昔单抗(BR)相比,无进展生存期(PFS)和总生存期(OS)更优。我们报告了MURANO试验的最终分析结果(中位随访时间为7年)。患者被随机分为VenR组(维奈克拉每日400 mg,持续2年加每月一次利妥昔单抗,共6个月;n = 194)或BR组(6个月;n = 195)。在一项子研究中,疾病进展(PD)的患者接受VenR作为再治疗或从BR组交叉过来接受治疗。在最终数据截止时(2022年8月3日),VenR组的中位PFS为54.7个月,而BR组为17.0个月。VenR组的7年PFS率为23.0%。7年OS率分别为69.6%和51.0%。在VenR治疗的患者中,治疗结束时(EOT)检测不到微小残留病(MRD;uMRD)且无PD的患者(n = 83),从EOT开始的中位PFS为52.5个月,而EOT时存在MRD的患者(n = 35;P <.0001)为18.0个月。14名患者实现了持久的uMRD。在4名患者中鉴定出BCL2的三种不同突变。在子研究中,25名患者接受VenR再治疗,9名患者交叉接受VenR治疗;中位PFS分别为23个月和27个月,最佳总体缓解率分别为72%和89%。在联合治疗结束时(EOCT),再治疗或交叉治疗后,分别有8名和6名患者实现了uMRD。未观察到新的安全性发现。总体而言,这些MURANO试验的最终分析支持考虑对复发/难治性CLL患者采用固定疗程的VenR治疗。该试验在www.clinicaltrials.gov上注册,注册号为#NCT02005471。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验