医学
内科学
白细胞减少症
中止
不利影响
外周T细胞淋巴瘤
胃肠病学
淋巴瘤
肿瘤科
队列
维持疗法
完全响应
临床研究阶段
无进展生存期
淋巴细胞减少症
外围设备
白细胞
进行性疾病
化疗
T细胞
淋巴细胞
存活率
外科
生存分析
癌症
外周血
毒性
中性粒细胞绝对计数
化学免疫疗法
队列研究
全血细胞计数
回顾性队列研究
作者
Juying Wei,Qingqing Cai,Liling Zhang,Liqun Zou,Zengjun Li,Keshu Zhou,Huijing Wu,L. Qiu,L. Joseph Su,Kaiyang Ding,Hui Zhou,Lei Yu,Fei Li,W P Li,Li’e Lin,Qing Xiao,Erhua Wang,Hongmei Jing,Mimi Zheng,Hongyu Zhang
标识
DOI:10.1038/s41408-026-01452-8
摘要
Patients with peripheral T cell lymphoma (PTCL) who achieved tumor response with first-line standard therapy were at high risk of disease relapse. We explored golidocitinib (150 mg once daily) as maintenance therapy for this group of patients (JACKPOT26, NCT06511869). This study included two cohorts: patients achieving a complete response (Cohort 1 (CR), N = 30) and a partial response (Cohort 2 (PR), N = 18) during induction stage. All enrolled patients were transplant ineligible or did not have a transplant plan. All dosed patients were included in the efficacy and safety analysis. In Cohort 1, the 24-month disease free survival (DFS) rate was 74.2% with golidocitinib treatment. In nodal subtypes (AITL, NOS, ALK- ALCL), the 24-month DFS rate was 62.7%. In Cohort 2, median progression free survival (PFS) was 17.4 months, and 24-month PFS rate was 48.6%. Nine out of 18 patients with initial PR achieved complete response, leading to a complete response rate of 50.0%, and median duration of response of 23.9 months. The most common ≥grade 3 treatment-related treatment-emergent adverse events (TRAEs) were hematological adverse events in nature, including neutrophil count decreased (47.9%), white blood cell count decreased (31.3%), lymphocyte count decreased (14.6%) and leukopenia (12.5%). The majority of these TRAEs were reversible and clinically manageable. TRAEs leading to treatment interruption and discontinuation occurred in 60.4% and 10% of patients, respectively. No TRAEs leading to fatal outcomes were reported. This study suggests the potential of golidocitinib as maintenance therapy for patients with PTCL.
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