drugset / Trial / NCT07542912

Sintilimab, Chidamide, and Azacitidine for Untreated Stage I-II Extranodal NK/T-Cell Lymphoma

NCT07542912

Not yet recruiting 30 enrolled Sun Yat-sen University
NaSingle-groupOpen-labelTreatment

Summary

This is an open-label, single-arm, multi-center Phase II clinical trial evaluating the efficacy and safety of a novel sequential regimen as first-line therapy for treatment-naïve patients with Extranodal NK/T-cell Lymphoma (ENKTL). The study consists of a Screening Phase, a Safety Lead-in Phase, and a Treatment Phase. During the Safety Lead-in Phase, 6 patients will be enrolled to receive a fixed dose of Sintilimab and Chidamide combined with Azacitidine to verify the dose (testing 100mg/d on days 1-3 versus days 1-5). Following the lead-in, all subjects will undergo a 2-cycle Immunotherapy Induction Phase with the SCA regimen (Sintilimab, Chidamide, and Azacitidine). Subsequently, treatment will be stratified based on response: patients achieving Complete Response (CR) or Partial Response (PR) will receive 4 additional cycles of SCA consolidation, while those with Stable Disease (SD) or Progressive Disease (PD) will switch to 4 cycles of P-GemOx chemotherapy. Upon completion of systemic therapy, all patients will undergo consolidative involved-field radiotherapy (≥50Gy).

Timeline

Start
2026-06-01
Primary completion
2029-06-01
Completion
2029-06-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Azacitidine Other / unclassified 100 mg
Subject Gemcitabine Small molecule
Subject Oxaliplatin Small molecule
Subject Pemetrexed Small molecule
Subject Sintilimab Monoclonal antibody 200 mg
Subject Tucidinostat Small molecule 30 mg

Indications

No indication recorded.