Total Body Irradiation or Chemotherapy Conditioning in Childhood ALL: A Multinational, Randomized, Noninferiority Phase III Study.
Adolescent
Antineoplastic Combined Chemotherapy Protocols
/ therapeutic use
Busulfan
/ administration & dosage
Chemoradiotherapy
/ mortality
Child
Child, Preschool
Equivalence Trials as Topic
Etoposide
/ administration & dosage
Female
Follow-Up Studies
Humans
International Agencies
Male
Precursor Cell Lymphoblastic Leukemia-Lymphoma
/ pathology
Prognosis
Survival Rate
Thiotepa
/ administration & dosage
Vidarabine
/ administration & dosage
Whole-Body Irradiation
/ mortality
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 2021
01 02 2021
Historique:
pubmed:
18
12
2020
medline:
28
8
2021
entrez:
17
12
2020
Statut:
ppublish
Résumé
Total body irradiation (TBI) before allogeneic hematopoietic stem cell transplantation (HSCT) in pediatric patients with acute lymphoblastic leukemia (ALL) is efficacious, but long-term side effects are concerning. We investigated whether preparative combination chemotherapy could replace TBI in such patients. FORUM is a randomized, controlled, open-label, international, multicenter, phase III, noninferiority study. Patients ≤ 18 years at diagnosis, 4-21 years at HSCT, in complete remission pre-HSCT, and with an HLA-compatible related or unrelated donor were randomly assigned to myeloablative conditioning with fractionated 12 Gy TBI and etoposide versus fludarabine, thiotepa, and either busulfan or treosulfan. The noninferiority margin was 8%. With 1,000 patients randomly assigned in 5 years, 2-year minimum follow-up, and one-sided alpha of 5%, 80% power was calculated. A futility stopping rule would halt random assignment if chemoconditioning was significantly inferior to TBI (EudraCT: 2012-003032-22; ClinicalTrials.gov: NCT01949129). Between April 2013 and December 2018, 543 patients were screened, 417 were randomly assigned, 212 received TBI, and 201 received chemoconditioning. The stopping rule was applied on March 31, 2019. The median follow-up was 2.1 years. In the intention-to-treat population, 2-year overall survival (OS) was significantly higher following TBI (0.91; 95% CI, 0.86 to 0.95; Improved OS and lower relapse risk were observed following TBI plus etoposide compared with chemoconditioning. We therefore recommend TBI plus etoposide for patients > 4 years old with high-risk ALL undergoing allogeneic HSCT.
Identifiants
pubmed: 33332189
doi: 10.1200/JCO.20.02529
pmc: PMC8078415
doi:
Substances chimiques
Etoposide
6PLQ3CP4P3
Thiotepa
905Z5W3GKH
treosulfan
CO61ER3EPI
Vidarabine
FA2DM6879K
Busulfan
G1LN9045DK
fludarabine
P2K93U8740
Banques de données
ClinicalTrials.gov
['NCT01949129']
EudraCT
['2012-003032-22']
Types de publication
Clinical Trial, Phase III
Journal Article
Multicenter Study
Randomized Controlled Trial
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
295-307Commentaires et corrections
Type : CommentIn
Type : CommentIn
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