Efficacy of chidamide maintenance therapy versus autologous stem cell transplantation versus observation as a post-remission choice in the survival of adult patients with peripheral T-cell lymphoma: Post hoc analysis of a prospective, multicenter, phase 2 study in China.
Wei WangWei ZhangLi-Ping SuLi-Hong LiuYu-Huan GaoQuan-Shun WangHang SuYu-Qin SongHui-Lai ZhangJing ShenHong-Mei JingShu-Ye WangXi-Nan CenHui LiuAi-Chun LiuZeng-Jun LiJian-Min LuoJian-Xia HeJing-Wen WangO A O'ConnorDao-Bin ZhouPublished in: Annals of hematology (2024)
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 .
Keyphrases
- stem cell transplantation
- clinical trial
- free survival
- high dose
- end stage renal disease
- newly diagnosed
- chronic kidney disease
- ejection fraction
- double blind
- bone marrow
- computed tomography
- open label
- type diabetes
- magnetic resonance
- rheumatoid arthritis
- squamous cell carcinoma
- randomized controlled trial
- cross sectional
- drug delivery
- cell therapy
- skeletal muscle
- disease activity
- patient reported
- risk assessment
- platelet rich plasma
- cancer therapy
- climate change
- phase iii
- human health
- positron emission tomography
- decision making
- placebo controlled
- rectal cancer
- replacement therapy