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口服 HDAC 抑制剂 tucidinostat 治疗复发或难治性外周 T 细胞淋巴瘤:Ⅱb 期结果。

Oral HDAC inhibitor tucidinostat in patients with relapsed or refractory peripheral T-cell lymphoma: phase IIb results.

机构信息

Kindai University Hospital, Osaka-Sayama.

Samsung Medical Center Sungkyunkwan University School of Medicine, Seoul.

出版信息

Haematologica. 2023 Mar 1;108(3):811-821. doi: 10.3324/haematol.2022.280996.

Abstract

Tucidinostat (formerly known as chidamide) is an orally available, novel benzamide class of histone deacetylase (HDAC) inhibitor that selectively blocks class I and class IIb HDAC. This multicenter phase IIb study aimed to investigate the efficacy and safety of tucidinostat, 40 mg twice per week (BIW), in patients with relapsed/refractory (R/R) peripheral T-cell lymphoma (PTCL). The primary endpoint was overall response rate (ORR) assessed by an independent overall efficacy review committee. Between March 2017 and March 2019, 55 patients were treated, and 46 and 55 were evaluated for efficacy and safety, respectively. Twenty-one of 46 patients achieved objective responses with an ORR of 46% (95% confidence interval : 30.9-61.0), including five patients with complete response (CR). Responses were observed across various PTCL subtypes. In angioimmunoblastic T-cell lymphoma, there were two CR and five partial responses (PR) among eight patients, achieving an ORR of 88%. The disease control rate (CR + PR + stable disease) was 72% (33/46). The median progression-free survival, duration of response, and overall survival were 5.6 months, 11.5 months, 22.8 months, respectively. The most common adverse events (AE) (all grades) were thrombocytopenia, neutropenia, leukopenia, anemia, and diarrhea. The grade ≥3 AE emerging in ≥20% of patients included thrombocytopenia (51%), neutropenia (36%), lymphopenia (22%), and leukopenia (20%). Importantly, most of the AE were manageable by supportive care and dose modification. In conclusion, the favorable efficacy and safety profiles indicate that tucidinostat could be a new therapeutic option in patients with R/R PTCL (clinicaltrials gov. Identifier: NCT02953652).

摘要

图昔单抗(原名为西达本胺)是一种新型口服苯甲酰胺类组蛋白去乙酰化酶(HDAC)抑制剂,能选择性抑制 I 类和 IIb 类 HDAC。这项多中心的 IIb 期研究旨在评估每周两次(BIW)、40mg 剂量的图昔单抗治疗复发/难治性(R/R)外周 T 细胞淋巴瘤(PTCL)患者的疗效和安全性。主要终点是由独立的总体疗效评估委员会评估的总体缓解率(ORR)。2017 年 3 月至 2019 年 3 月,共治疗了 55 例患者,分别有 46 例和 55 例患者接受了疗效和安全性评估。46 例患者中有 21 例达到了客观缓解,ORR 为 46%(95%置信区间:30.9-61.0),包括 5 例完全缓解(CR)。各种 PTCL 亚型均观察到了缓解。在血管免疫母细胞性 T 细胞淋巴瘤中,8 例患者中有 2 例 CR 和 5 例 PR,ORR 为 88%。疾病控制率(CR+PR+稳定疾病)为 72%(33/46)。中位无进展生存期、缓解持续时间和总生存期分别为 5.6 个月、11.5 个月和 22.8 个月。最常见的不良反应(AE)(所有级别)为血小板减少、中性粒细胞减少、白细胞减少、贫血和腹泻。≥20%的患者出现的≥3 级 AE 包括血小板减少(51%)、中性粒细胞减少(36%)、淋巴细胞减少(22%)和白细胞减少(20%)。重要的是,大多数 AE 通过支持性治疗和剂量调整是可以控制的。总之,图昔单抗具有良好的疗效和安全性,可作为 R/R PTCL 患者的一种新的治疗选择(clinicaltrials.gov 标识符:NCT02953652)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c177/9973490/875618042f82/108811.fig1.jpg

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