Low-dose chidamide maintenance therapy following allogeneic hematopoietic cell transplantation in T-cell acute lymphoblastic leukemia or lymphomas: a phase II, open-label, multicenter, single-arm trial
- Journal
- The Lancet regional health. Western Pacific (Q1)
- Published
- 13 July 2026
- Study design
- Non-randomized / quasi-experimental trial
- Evidence level
- Level 2, Moderate (CEBM 2b)
- Authors
- Yanmin Zhao, Weihao Chen, Yi Yu, Yi Luo, Jian Yu, Huarui Fu, et al.
- PMID
- 42518787
- DOI
- 10.1016/j.lanwpc.2026.101916
Why clinicians should know about it
- Picked for Transplantation (paper of the day, 29 July 2026): Low‑dose chidamide maintenance reduces relapse after allo‑HCT for T‑ALL/TCL
Abstract
BACKGROUND: Despite allogeneic hematopoietic cell transplantation (allo-HCT), relapse remains a leading cause of treatment failure for patients with T-cell acute lymphoblastic leukemia (T-ALL) or T-cell lymphomas (TCL). Given the immunomodulatory properties of histone deacetylase inhibitors, this phase II trial (NCT05991973) investigated chidamide maintenance to reduce post-transplant relapse risk for T-ALL/TCL. METHODS: In this multicenter, open-label study, patients aged 14-70 years in remission after first allo-HCT received oral chidamide (10 mg twice weekly) for up to 96 weeks. The primary endpoint was 2-year relapse-free survival (RFS). Secondary endpoints included overall survival (OS), cumulative incidence of relapse (CIR), non-relapse mortality (NRM), chronic GVHD, and safety. Outcomes were also compared post hoc with a matched control cohort without maintenance therapy. FINDINGS: Between July 2023 and August 2024, 44 patients were enrolled. At a median follow-up of 24.3 months (IQR 18.2-25.7), the 2-year RFS was 83.7% (95% CI 73.3%-95.6%). Secondary endpoints showed a 2-year OS of 89.6% (80.3%-100%), CIR of 11.8% (1.9%-21.7%), NRM of 4.5% (0%-10.7%), and chronic GVHD of 38.3% (23.0%-53.5%). Treatment-emergent adverse events were predominantly grade 1-2 and manageable. The most frequent events were leukopenia (5 [11%]), thrombocytopenia (5 [11%]) and nausea or vomiting (5 [11%]). INTERPRETATION: Chidamide as maintenance could be a potential prophylactic strategy of relapse after allo-HCT for T-ALL/TCL, warranting further confirmation through phase III trials. FUNDING: National Key Research and Development Program of China; National Natural Science Foundation of China; Zhejiang Provincial Natural Science Foundation of China.
Abstract as published, via PubMed.
For healthcare professionals. The summary is generated by AI from the published abstract, and the evidence level is assigned automatically from the study design on the Oxford CEBM hierarchy. Neither is medical advice. Read the full paper before changing practice.