Department of Hematology, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Department of Medical Oncology, Guangxi Medical University Affiliated Tumor Hospital, Nanning, China.
Clin Cancer Res. 2024 Oct 15;30(20):4593-4600. doi: 10.1158/1078-0432.CCR-24-1194.
Relapsed and/or refractory peripheral T-cell lymphoma (r/r PTCL) is an aggressive and heterogeneous hematologic malignancy with high unmet need. Previously, PI3K inhibitors were shown to be efficacious in B- and T-cell lymphomas, but as a drug class, these agents have frequently been observed to have tolerability limitations. Next-generation agents that improve the tolerability while maintaining efficacy are desirable.
A phase Ib clinical study was conducted with the oral PI3K-delta isoform-selective small-molecule inhibitor, linperlisib, in patients with r/r PTCL, and the clinical benefit was explored by the evaluation of safety and efficacy.
In this clinical study, 43 patients with r/r PTCL in China were treated with continuous dosing of 80-mg linperlisib once a day. Treatment-related adverse events (AE) were manageable. The most frequently reported grade 3 AE were neutropenia (21%), pneumonia (11.6%), and hypertriglyceridemia (7%). All other AE were either absent or reported in <5% of the patients. Linperlisib treatment for these patients with r/r PTCL, consisting of the major PTCL subtypes, was observed to have a 60.5% overall response rate with 35% complete responses and led to a median duration of response of 11.1 months, median progression-free survival of 11.8 months, and a median overall survival of >38 months (not reached).
With the very promising clinical activity against r/r PTCL, the results of this study support the further investigation of linperlisib for the treatment of r/r PTCL.
复发/难治性外周 T 细胞淋巴瘤(r/rPTCL)是一种侵袭性和异质性血液恶性肿瘤,存在未满足的巨大需求。先前的研究表明,PI3K 抑制剂在 B 细胞和 T 细胞淋巴瘤中具有疗效,但作为一个药物类别,这些药物经常表现出耐受性限制。因此,需要开发能够改善耐受性同时保持疗效的新一代药物。
一项针对复发/难治性外周 T 细胞淋巴瘤患者的口服 PI3K-δ 同工型选择性小分子抑制剂 linperlisib 的 Ib 期临床研究,通过评估安全性和疗效来探索临床获益。
在这项临床研究中,中国 43 例复发/难治性外周 T 细胞淋巴瘤患者接受了连续剂量为 80mg 每天一次的 linperlisib 治疗。治疗相关不良反应(AE)可管理。最常见的 3 级 AE 为中性粒细胞减少症(21%)、肺炎(11.6%)和高甘油三酯血症(7%)。其他所有 AE 要么不存在,要么报告的患者比例<5%。linperlisib 治疗 r/rPTCL 患者,包括主要的 PTCL 亚型,观察到总缓解率为 60.5%,完全缓解率为 35%,中位缓解持续时间为 11.1 个月,中位无进展生存期为 11.8 个月,中位总生存期>38 个月(未达到)。
鉴于 linperlisib 对 r/rPTCL 具有非常有前景的临床活性,本研究结果支持进一步研究 linperlisib 治疗 r/rPTCL。