Dose-Adjusted Etoposide, Doxorubicin, and Cyclophosphamide With Vincristine and Prednisone Plus Rituximab Therapy in Children and Adolescents With Primary Mediastinal B-Cell Lymphoma: A Multicenter Phase II Trial.
Adolescent
Antineoplastic Combined Chemotherapy Protocols
/ therapeutic use
Child
Cyclophosphamide
/ administration & dosage
Dose-Response Relationship, Drug
Doxorubicin
/ administration & dosage
Etoposide
/ administration & dosage
Female
Follow-Up Studies
Humans
Lymphoma, Follicular
/ drug therapy
Lymphoma, Large B-Cell, Diffuse
/ drug therapy
Male
Mediastinal Neoplasms
/ drug therapy
Prednisone
/ administration & dosage
Prognosis
Prospective Studies
Rituximab
/ administration & dosage
Vincristine
/ administration & dosage
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:
20 11 2021
20 11 2021
Historique:
pubmed:
28
9
2021
medline:
28
12
2021
entrez:
27
9
2021
Statut:
ppublish
Résumé
A dose-adjusted etoposide, doxorubicin, and cyclophosphamide with vincristine and prednisone plus rituximab (DA-EPOCH-R) regimen has been shown to deliver excellent survival for adults with primary mediastinal large B-cell lymphoma (PMLBL) without the use of radiotherapy. No international prospective evaluation of this regimen has previously been reported in children and adolescents. We conducted an international single-arm phase II trial involving patients younger than age 18 years with PMLBL who were to receive six courses of DA-EPOCH-R. The primary end point was event-free survival (EFS). Overall survival and toxicity were also assessed. This trial was registered (ClinicalTrials.gov identifier: NCT01516567). Analyses were based on 46 patients. The median age was 15.4 years (interquartile range: 14-16 years). The median follow-up was 59.0 months (interquartile range: 52.6-69.2 months). Fourteen events were observed (eight relapses or progressions (including three parenchymal CNS relapses), four residual lymphoma, and two second malignancies). The 4-year EFS was 69.6% (95% CI, 55.2 to 80.9), which did not differ from the rate observed historically ( DA-EPOCH-R did not improve the EFS compared with a historical control in this first prospective multisite international study of children and adolescents with PMLBL. Further studies are required to determine the optimum therapy for children and adolescents with this lymphoma.
Identifiants
pubmed: 34570655
doi: 10.1200/JCO.21.00920
pmc: PMC9150887
doi:
Substances chimiques
Rituximab
4F4X42SYQ6
Vincristine
5J49Q6B70F
Etoposide
6PLQ3CP4P3
Doxorubicin
80168379AG
Cyclophosphamide
8N3DW7272P
Prednisone
VB0R961HZT
Banques de données
ClinicalTrials.gov
['NCT01516567']
Types de publication
Clinical Trial, Phase II
Journal Article
Multicenter Study
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
3716-3724Subventions
Organisme : Cancer Research UK
ID : 13336
Pays : United Kingdom
Organisme : NCI NIH HHS
ID : U10 CA180886
Pays : United States
Organisme : NCI NIH HHS
ID : U10 CA180899
Pays : United States
Organisme : Department of Health
Pays : United Kingdom
Commentaires et corrections
Type : CommentIn
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