Treatment of Childhood Nasopharyngeal Carcinoma With Induction Chemotherapy and Concurrent Chemoradiotherapy: Results of the Children's Oncology Group ARAR0331 Study.


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:
10 12 2019
Historique:
pubmed: 26 9 2019
medline: 17 6 2020
entrez: 26 9 2019
Statut: ppublish

Résumé

The treatment of childhood nasopharyngeal carcinoma has been adapted from adult regimens; pediatric-specific studies are limited. The ARAR0331 study sought to evaluate the impact of induction chemotherapy (IC) and concurrent chemoradiotherapy (CCR). Patients with American Joint Committee on Cancer stages IIb to IV were scheduled to receive three cycles of IC with cisplatin and fluorouracil, followed by CCR with three cycles of cisplatin. Patients with complete or partial response to IC received 61.2 Gy to the nasopharynx and neck, and patients with stable disease received 71.2 Gy. Between February 2006 and January 2012, 111 patients (75 male) were enrolled. Median age was 15 years, and 46.8% of the patients were African American. After a feasibility analysis, the study was amended to reduce cisplatin to two cycles during CCR. The 5-year event-free survival (EFS) and overall survival estimates were 84.3% and 89.2%, respectively. The 5-year EFS for stages IIb, III, and IV were 100%, 82.8%, and 82.7%, respectively. The 5-year cumulative incidence estimates of local, distant, and combined relapse were 3.7%, 8.7%, and 1.8%, respectively. Patients treated with three versus two CCR cycles of cisplatin had improved 5-year postinduction EFS (90.7% Patients in ARAR0331 were characterized by advanced disease and by a high proportion of black children and adolescents. Treatment with IC and CRT resulted in excellent outcomes. A radiation dose reduction is possible for patients responding to IC. Although the outcomes are comparable, we observed a trend toward decreased EFS for patients assigned to receive fewer doses of cisplatin during CCR.

Identifiants

pubmed: 31553639
doi: 10.1200/JCO.19.01276
pmc: PMC6920031
doi:

Substances chimiques

Cisplatin Q20Q21Q62J
Fluorouracil U3P01618RT

Banques de données

ClinicalTrials.gov
['NCT00274937']

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

3369-3376

Subventions

Organisme : NCI NIH HHS
ID : U10 CA029511
Pays : United States
Organisme : NCATS NIH HHS
ID : UL1 TR001863
Pays : United States
Organisme : NCI NIH HHS
ID : U10 CA098413
Pays : United States
Organisme : NCI NIH HHS
ID : U10 CA098543
Pays : United States
Organisme : NCI NIH HHS
ID : U10 CA180899
Pays : United States
Organisme : NCI NIH HHS
ID : U10 CA180886
Pays : United States

Commentaires et corrections

Type : ErratumIn

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Auteurs

Carlos Rodriguez-Galindo (C)

St Jude Children's Research Hospital, Memphis, TN.

Mark D Krailo (MD)

Children's Oncology Group, Monrovia, CA.
University of Southern California, Los Angeles, CA.

Matthew J Krasin (MJ)

St Jude Children's Research Hospital, Memphis, TN.

Li Huang (L)

Children's Oncology Group, Monrovia, CA.

M Beth McCarville (MB)

St Jude Children's Research Hospital, Memphis, TN.

John Hicks (J)

Texas Children's Hospital, Houston, TX.

Farzana Pashankar (F)

Yale University School of Medicine, New Haven, CT.

Alberto S Pappo (AS)

St Jude Children's Research Hospital, Memphis, TN.

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Classifications MeSH