Department of Hematology, Peking Union Medical College Hospital, 1, Shuaifuyuan Wangfujing, Dongcheng District, Beijing, 100730, China.
Department of Hematology, Shanxi Provincial Cancer Hospital, 3 Worker's New Village, Xinghualing District, Taiyuan, Shanxi, China.
Ann Hematol. 2024 Aug;103(8):3061-3069. doi: 10.1007/s00277-024-05708-w. Epub 2024 May 28.
In this prospective, multicenter, Phase 2 clinical trial (NCT02987244), patients with peripheral T-cell lymphomas (PTCLs) who had responded to first-line chemotherapy with cyclophosphamide, doxorubicin or epirubicin, vincristine or vindesine, etoposide, and prednisone (Chi-CHOEP) were treated by autologous stem cell transplantation (ASCT) or with chidamide maintenance or observation. A total of 85 patients received one of the following interventions: ASCT (n = 15), chidamide maintenance (n = 44), and observation (n = 26). estimated 3 PFS and OS rates were 85.6%, 80.8%, and 49.4% (P = 0.001). The two-year OS rates were 85.6%, 80.8%, and 69.0% (P = 0.075).The ASCT and chidamide maintenance groups had significantly better progression-free survival (PFS) than the observation group (P = 0.001, and P = 0.01, respectively). The overall survival (OS) differed significantly between the chidamide maintenance group and the observation group ( P = 0.041). The multivariate and propensity score matching analyses for PFS revealed better outcomes in the subjects in the chidamide maintenance than observation groups (P = 0.02). The ASCT and chidamide maintenance groups had significant survival advantages over the observation group. In the post-remission stage of the untreated PTCL patients, single-agent chidamide maintenance demonstrated superior PFS and better OS than observation. Our findings highlight the potential benefit of chidamide in this patient subset, warranting further investigation through larger prospective trials. Clinical trial registration: clinicaltrial.gov, NCT02987244. Registered 8 December 2016, http://www.clinicaltrials.gov/ct2/show/NCT02987244 .
在这项前瞻性、多中心、2 期临床试验(NCT02987244)中,对一线化疗(环磷酰胺、多柔比星或表柔比星、长春新碱或长春地辛、依托泊苷和泼尼松)治疗后有反应的外周 T 细胞淋巴瘤(PTCL)患者进行了自体造血干细胞移植(ASCT)或西达本胺维持治疗或观察。共有 85 例患者接受了以下干预措施之一:ASCT(n=15)、西达本胺维持治疗(n=44)和观察(n=26)。估计的 3 年无进展生存期(PFS)和总生存期(OS)率分别为 85.6%、80.8%和 49.4%(P=0.001)。2 年 OS 率分别为 85.6%、80.8%和 69.0%(P=0.075)。ASCT 组和西达本胺维持治疗组的无进展生存(PFS)明显优于观察组(P=0.001 和 P=0.01)。西达本胺维持治疗组与观察组的总生存(OS)差异有统计学意义(P=0.041)。多变量和倾向评分匹配分析显示,西达本胺维持治疗组患者的预后明显优于观察组(P=0.02)。ASCT 组和西达本胺维持治疗组的生存明显优于观察组。在未经治疗的 PTCL 患者的缓解后阶段,西达本胺单药维持治疗显示出比观察更好的 PFS 和 OS。我们的研究结果突出了西达本胺在这一患者亚组中的潜在获益,需要通过更大规模的前瞻性试验进一步研究。临床试验注册:clinicaltrial.gov,NCT02987244。于 2016 年 12 月 8 日注册,http://www.clinicaltrials.gov/ct2/show/NCT02987244。