Randomized Phase III BMT CTN Trial of Calcineurin Inhibitor-Free Chronic Graft-Versus-Host Disease Interventions in Myeloablative Hematopoietic Cell Transplantation for Hematologic Malignancies.
Adolescent
Adult
Aged
Calcineurin Inhibitors
/ adverse effects
Chronic Disease
Cyclophosphamide
/ adverse effects
Disease-Free Survival
Drug Therapy, Combination
Female
Germany
Graft vs Host Disease
/ diagnosis
Hematologic Neoplasms
/ diagnosis
Hematopoietic Stem Cell Transplantation
/ adverse effects
Humans
Immunosuppressive Agents
/ adverse effects
Male
Methotrexate
/ adverse effects
Middle Aged
Myeloablative Agonists
/ adverse effects
Recurrence
Tacrolimus
/ adverse effects
Time Factors
Transplantation Conditioning
/ adverse effects
United States
Young Adult
Journal
Journal of clinical oncology : official journal of the American Society of Clinical Oncology
ISSN: 1527-7755
Titre abrégé: J Clin Oncol
Pays: United States
ID NLM: 8309333
Informations de publication
Date de publication:
01 02 2022
01 02 2022
Historique:
pubmed:
3
12
2021
medline:
22
2
2022
entrez:
2
12
2021
Statut:
ppublish
Résumé
Calcineurin inhibitors (CNI) are standard components of graft-versus-host disease (GVHD) prophylaxis after hematopoietic cell transplantation (HCT). Prior data suggested that CNI-free approaches using donor T-cell depletion, either by ex vivo CD34 selection or in vivo post-transplant cyclophosphamide (PTCy) as a single agent, are associated with lower rates of chronic GVHD (cGVHD). This multicenter phase III trial randomly assigned patients with acute leukemia or myelodysplasia and an HLA-matched donor to receive CD34-selected peripheral blood stem cell, PTCy after a bone marrow (BM) graft, or tacrolimus and methotrexate after BM graft (control). The primary end point was cGVHD (moderate or severe) or relapse-free survival (CRFS). Among 346 patients enrolled, 327 received HCT, 300 per protocol. Intent-to-treat rates of 2-year CRFS were 50.6% for CD34 selection (hazard ratio [HR] compared with control, 0.80; 95% CI, 0.56 to 1.15; CNI-free interventions as performed herein did not result in superior CRFS compared with tacrolimus and methotrexate with BM. Lower rates of moderate and severe cGVHD did not translate into improved survival.
Identifiants
pubmed: 34855460
doi: 10.1200/JCO.21.02293
pmc: PMC8797487
doi:
Substances chimiques
Calcineurin Inhibitors
0
Immunosuppressive Agents
0
Myeloablative Agonists
0
Cyclophosphamide
8N3DW7272P
Tacrolimus
WM0HAQ4WNM
Methotrexate
YL5FZ2Y5U1
Banques de données
ClinicalTrials.gov
['NCT02345850']
Types de publication
Clinical Trial, Phase III
Journal Article
Multicenter Study
Randomized Controlled Trial
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
356-368Subventions
Organisme : NHLBI NIH HHS
ID : UG1 HL109322
Pays : United States
Organisme : NHLBI NIH HHS
ID : U01 HL069310
Pays : United States
Organisme : NHLBI NIH HHS
ID : UG1 HL069249
Pays : United States
Organisme : NHLBI NIH HHS
ID : UG1 HL069310
Pays : United States
Organisme : NHLBI NIH HHS
ID : UG1 HL108945
Pays : United States
Organisme : NHLBI NIH HHS
ID : UG1 HL108987
Pays : United States
Organisme : NCI NIH HHS
ID : P30 CA008748
Pays : United States
Organisme : NHLBI NIH HHS
ID : UG1 HL069291
Pays : United States
Organisme : NHLBI NIH HHS
ID : UG1 HL069315
Pays : United States
Organisme : NHLBI NIH HHS
ID : UG1 HL138645
Pays : United States
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