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阿卡拉布替尼、维奈克拉和奥滨尤妥珠单抗用于复发/难治性慢性淋巴细胞白血病:CLL2-BAAG试验的最终疗效及循环肿瘤DNA分析

Acalabrutinib, venetoclax, and obinutuzumab in relapsed/refractory CLL: final efficacy and ctDNA analysis of the CLL2-BAAG trial.

作者信息

Fürstenau Moritz, Giza Adam, Weiss Jonathan, Kleinert Fanni, Robrecht Sandra, Franzen Fabian, Stumpf Janina, Langerbeins Petra, Al-Sawaf Othman, Simon Florian, Fink Anna-Maria, Schneider Christof, Tausch Eugen, Schetelig Johannes, Dreger Peter, Böttcher Sebastian, Fischer Kirsten, Kreuzer Karl-Anton, Ritgen Matthias, Schilhabel Anke, Brüggemann Monika, Stilgenbauer Stephan, Eichhorst Barbara, Hallek Michael, Cramer Paula

机构信息

Department I of Internal Medicine, Faculty of Medicine and University Hospital of Cologne, Center for Integrated Oncology Aachen Bonn Cologne Duesseldorf, German Chronic Lymphocytic Leukemia Study Group, University of Cologne, Cologne, Germany.

Division of Chronic Lymphocytic Leukemia, Department of Internal Medicine III, University Hospital Ulm, Ulm, Germany.

出版信息

Blood. 2024 Jul 18;144(3):272-282. doi: 10.1182/blood.2023022730.

Abstract

The phase 2 CLL2-BAAG trial tested the measurable residual disease (MRD)-guided triple combination of acalabrutinib, venetoclax, and obinutuzumab after optional bendamustine debulking in 45 patients with relapsed/refractory chronic lymphocytic leukemia (CLL). MRD was measured by flow cytometry (FCM; undetectable MRD <10-4) in peripheral blood (PB) and circulating tumor DNA (ctDNA) using digital droplet polymerase chain reaction of variable-diversity-joining (VDJ) rearrangements and CLL-related mutations in plasma. The median number of previous treatments was 1 (range, 1-4); 18 patients (40%) had received a Bruton tyrosine kinase inhibitor (BTKi) and/or venetoclax before inclusion, 14 of 44 (31.8%) had TP53 aberrations, and 34 (75.6%) had unmutated immunoglobulin heavy-chain variable region genes. With a median observation time of 36.3 months and all patients off-treatment for a median of 21.9 months, uMRD <10-4 in PB was achieved in 42 of the 45 patients (93.3%) at any time point, including 17 of 18 (94.4%) previously exposed to venetoclax/BTKi and 13 of 14 (92.9%) with TP53 aberrations. The estimated 3-year progression-free and overall survival rates were 85.0% and 93.8%, respectively. Overall, 585 paired FCM/ctDNA samples were analyzed and 18 MRD recurrences (5 with and 13 without clinical progression) occurred after the end of treatment. Twelve samples were first detected by ctDNA, 3 by FCM, and 3 synchronously. In conclusion, time-limited MRD-guided acalabrutinib, venetoclax, and obinutuzumab achieved deep remissions in almost all patients with relapsed/refractory CLL. The addition of ctDNA-based analyses to FCM MRD assessment seems to improve early detection of relapses. This trial was registered at www.clinicaltrials.gov as #NCT03787264.

摘要

2期CLL2-BAAG试验对45例复发/难治性慢性淋巴细胞白血病(CLL)患者在进行可选的苯达莫司汀减瘤治疗后,测试了基于可测量残留病(MRD)指导的阿卡拉布替尼、维奈克拉和奥妥珠单抗三联组合疗法。通过流式细胞术(FCM;不可检测的MRD<10-4)在外周血(PB)中测量MRD,并使用数字液滴聚合酶链反应检测血浆中可变区-多样性-连接(VDJ)重排和CLL相关突变的循环肿瘤DNA(ctDNA)。既往治疗的中位数为1次(范围1-4次);18例患者(40%)在入组前接受过布鲁顿酪氨酸激酶抑制剂(BTKi)和/或维奈克拉治疗,44例中的14例(31.8%)存在TP53畸变,34例(75.6%)的免疫球蛋白重链可变区基因未发生突变。中位观察时间为36.3个月,所有患者的中位停药时间为21.9个月,45例患者中有42例(93.3%)在任何时间点外周血中均可达到uMRD<10-4,包括18例中17例(94.4%)既往接受过维奈克拉/BTKi治疗的患者以及14例中13例(92.9%)存在TP53畸变的患者。估计3年无进展生存率和总生存率分别为85.0%和93.8%。总体而言,共分析了585对FCM/ctDNA样本,治疗结束后发生了18次MRD复发(5次伴有临床进展,13次无临床进展)。12个样本首先通过ctDNA检测到,3个通过FCM检测到,3个同步检测到。总之,限时的基于MRD指导的阿卡拉布替尼、维奈克拉和奥妥珠单抗疗法使几乎所有复发/难治性CLL患者实现了深度缓解。在FCM MRD评估中增加基于ctDNA的分析似乎可改善复发的早期检测。该试验已在www.clinicaltrials.gov注册,编号为#NCT03787264。

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