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在日本,对于 EZH2 突变的复发/难治性 B 细胞非霍奇金淋巴瘤患者使用 Tazemetostat:一项 II 期研究的 3 年随访。

Tazemetostat for relapsed/refractory B-cell non-Hodgkin lymphoma with EZH2 mutation in Japan: 3-year follow-up for a phase II study.

机构信息

Department of Hematology, National Cancer Center Hospital, 5-1-1 Tsukiji, Chuo-ku, Tokyo, 104-0045, Japan.

Department of Hematology and Oncology, Tokai University School of Medicine, Isehara, Japan.

出版信息

Int J Hematol. 2024 Nov;120(5):621-630. doi: 10.1007/s12185-024-03834-9. Epub 2024 Aug 23.

Abstract

Previously, we reported the efficacy and safety of tazemetostat in Japanese patients with relapsed/refractory follicular lymphoma (FL) and diffuse large B-cell lymphoma (DLBCL) harboring the EZH2 mutation in a multicenter, open-label, phase II study. Here, we present a follow-up analysis of tazemetostat at a long-term median follow-up of 35.0 months. Twenty patients were enrolled: 17 in the FL cohort and three in the DLBCL cohort. In the FL cohort, the objective response rate was 70.6%, consistent with the primary analysis, and the median progression-free survival (PFS) was not reached. The 24-month and 36-month PFS rates were 72.1% (95% confidence interval [CI] 41.5%-88.6%) and 64.1% (95% CI 33.7%-83.4%), respectively. The median duration of treatment was 30.2 months. After the primary analysis at a median follow-up of 12.9 months, grade 1-2 urinary tract infection, peripheral motor neuropathy, and hypogammaglobulinemia newly emerged, but the incidence of adverse events (AEs) did not increase notably during this follow-up period. No unexpected grade ≥ 3 treatment-related AEs were reported. Long-term oral monotherapy with tazemetostat showed favorable efficacy and safety profiles, indicating that it may be a useful third-line or later treatment option for patients with relapsed/refractory FL harboring the EZH2 mutation. Trial registration: ClinicalTrials.gov: NCT03456726.

摘要

先前,我们报道了在一项多中心、开放标签、二期研究中,EZH2 突变的复发性/难治性滤泡淋巴瘤 (FL) 和弥漫性大 B 细胞淋巴瘤 (DLBCL) 日本患者中,他泽莫司他的疗效和安全性。在此,我们报告了在长期中位数随访 35.0 个月时他泽莫司他的随访分析。共纳入 20 例患者:FL 队列 17 例,DLBCL 队列 3 例。在 FL 队列中,客观缓解率为 70.6%,与主要分析一致,无进展生存期(PFS)中位数未达到。24 个月和 36 个月的 PFS 率分别为 72.1%(95%可信区间 [CI] 41.5%-88.6%)和 64.1%(95% CI 33.7%-83.4%)。中位治疗持续时间为 30.2 个月。在主要分析中位随访 12.9 个月后,新出现了 1-2 级尿路感染、周围运动神经病和低丙种球蛋白血症,但在这一随访期间,不良事件(AE)的发生率没有显著增加。未报告意外的≥3 级治疗相关 AE。长期口服他泽莫司他单药治疗显示出良好的疗效和安全性,表明它可能是复发性/难治性 FL 患者 EZH2 突变的一种有用的三线或更后线治疗选择。试验注册:ClinicalTrials.gov:NCT03456726。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e74/11513718/5311586b61da/12185_2024_3834_Fig1_HTML.jpg

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