Allo-HSCT as First-line Consolidation in High-risk PTCL
Launched by PEKING UNIVERSITY PEOPLE'S HOSPITAL · Sep 13, 2018
Trial Information
Current as of May 28, 2025
Unknown status
Keywords
ClinConnect Summary
After primary diagnosis eligible patients receive 2 to 3 courses of CHOEP-21 with formal restaging after course 2. Patients with CR, PR or no change proceed to allo-HSCT. Donor selection: Matched sibling donor(MSD) is the first choice. An unrelated donor or haploidentical family donor search is performed in patients without sibling donor. The primary end point was 1 year progression-free survival. The secondary end points were complete commission rate, transplant-related mortality, overall survival, relapse rate and graft-versus-host disease (GVHD) . Following time is 2 years
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • Primary diagnosis of mature T-cell lymphoma, stage 2-4, or stage 1 with aa IPI\>=0
- • age \<= 60 years
- • KPS\>=70
- Exclusion Criteria:
- • stage I with aaIPI 0, ALCL ALK positive, T-lymphoblastic lymphoma, cutaneous T-cell lymphoma
- • HIV positivity
- • major organ dysfunction
- • pregnancy
- • patient unable to give informed consent
About Peking University People's Hospital
Peking University People's Hospital is a leading clinical research institution in China, renowned for its commitment to advancing medical knowledge and improving patient care through innovative clinical trials. Affiliated with Peking University, the hospital integrates cutting-edge research, comprehensive healthcare services, and a multidisciplinary team of experts to facilitate the development of new therapies and medical interventions. With a strong focus on patient safety and ethical standards, Peking University People's Hospital is dedicated to conducting rigorous clinical trials that contribute to the global medical community and enhance the quality of life for patients.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Beijing, , China
Patients applied
Trial Officials
Xiao-Jun Huang, MD
Principal Investigator
Peking University
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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