MURANO研究:VenR对复发/难治性CLL患者的最终分析和再治疗/交叉亚研究结果。

IF 21 1区 医学 Q1 HEMATOLOGY
Blood Pub Date : 2025-06-05 DOI:10.1182/blood.2024025525
Arnon P Kater, Rosemary Harrup, Thomas J Kipps, Barbara Eichhorst, Carolyn J Owen, Sarit Assouline, Nicole Lamanna, Tadeusz Robak, Javier de la Serna, Ulrich Jaeger, Guillaume Cartron, Marco Montillo, Clemens Mellink, Anton W Langerak, Brenda Chyla, Relja Popovic, Yanwen Jiang, Rosemary Millen, Marcus Lefebure, Maria Thadani-Mulero, Michelle Boyer, John F Seymour
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引用次数: 0

摘要

在 MURANO 3 期试验(NCT02005471)中,固定疗程的 Venetoclax-rituximab (VenR) 用于复发/难治性慢性淋巴细胞白血病(CLL)患者的无进展生存期(PFS)和总生存期(OS)优于苯达莫司汀-利妥昔单抗(BR)。我们报告了 MURANO 的最终分析结果(中位随访 7 年)。患者被随机分配到VenR(每天400毫克 Venetoclax,持续2年,加上每月利妥昔单抗,持续6个月;n=194)或BR(6个月;n=195)。在一项子研究中,进展性疾病 (PD) 患者接受 VenR 作为再治疗或从 BR 交叉治疗。在最终数据截止日(2022 年 8 月 3 日),VenR 的中位 PFS 为 54.7 个月,BR 为 17.0 个月。VenR的7年PFS为23.0%。七年 OS 分别为 69.6% 和 51.0%。在检测不到(u)微小残留病灶(MRD)且治疗结束(EOT)时无 PD 的 VenR 治疗患者中(n = 83),自 EOT 起的中位 PFS 为 52.5 个月,而 EOT 时有 MRD 的患者为 18.0 个月(n = 35;P < 0.0001)。14名患者有持久的uMRD。在四名患者中发现了 BCL2 的三种不同突变。在子研究中,25名患者接受了VenR治疗,9名患者交叉接受了VenR治疗;中位PFS分别为23个月和27个月,最佳总反应率分别为72%和89%。在联合治疗结束时,再治疗或交叉治疗后分别有 8 名和 6 名患者达到 uMRD。没有发现新的安全性问题。总体而言,这些最终的MURANO分析支持考虑对复发/难治性CLL患者采用固定疗程的VenR疗法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The MURANO study: final analysis and retreatment/crossover substudy results of VenR for patients with relapsed/refractory CLL.

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.

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来源期刊
Blood
Blood 医学-血液学
CiteScore
23.60
自引率
3.90%
发文量
955
审稿时长
1 months
期刊介绍: Blood, the official journal of the American Society of Hematology, published online and in print, provides an international forum for the publication of original articles describing basic laboratory, translational, and clinical investigations in hematology. Primary research articles will be published under the following scientific categories: Clinical Trials and Observations; Gene Therapy; Hematopoiesis and Stem Cells; Immunobiology and Immunotherapy scope; Myeloid Neoplasia; Lymphoid Neoplasia; Phagocytes, Granulocytes and Myelopoiesis; Platelets and Thrombopoiesis; Red Cells, Iron and Erythropoiesis; Thrombosis and Hemostasis; Transfusion Medicine; Transplantation; and Vascular Biology. Papers can be listed under more than one category as appropriate.
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