Treatment of Childhood Nasopharyngeal Carcinoma With Induction Chemotherapy and Concurrent Chemoradiotherapy: Results of the Children's Oncology Group ARAR0331 Study.
Adolescent
Antineoplastic Combined Chemotherapy Protocols
/ therapeutic use
Chemoradiotherapy
/ mortality
Child
Child, Preschool
Cisplatin
/ administration & dosage
Feasibility Studies
Female
Fluorouracil
/ administration & dosage
Follow-Up Studies
Humans
Induction Chemotherapy
/ mortality
Male
Nasopharyngeal Carcinoma
/ pathology
Nasopharyngeal Neoplasms
/ pathology
Neoplasm Recurrence, Local
/ pathology
Prognosis
Survival Rate
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
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
3369-3376Subventions
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
Références
J Immunother. 2010 Nov-Dec;33(9):983-90
pubmed: 20948438
Cancer. 2012 Oct 1;118(19):4892-900
pubmed: 22359313
Lancet Oncol. 2003 Jan;4(1):13-21
pubmed: 12517535
Medicine (Baltimore). 2016 Apr;95(17):e3445
pubmed: 27124036
J Clin Oncol. 2018 May 10;36(14):1412-1418
pubmed: 29584545
Cancer. 2012 May 15;118(10):2718-25
pubmed: 21918965
Int J Radiat Oncol Biol Phys. 2018 Oct 1;102(2):340-352
pubmed: 30191868
J Cancer. 2015 Jul 17;6(9):883-92
pubmed: 26284140
Cancer Chemother Pharmacol. 2016 Feb;77(2):289-98
pubmed: 26666649
Int J Cancer. 2019 Jul 1;145(1):295-305
pubmed: 30613964
Eur J Cancer. 2011 Mar;47(5):656-66
pubmed: 21112774
Medicine (Baltimore). 2019 Jul;98(28):e16327
pubmed: 31305420
Pediatr Blood Cancer. 2017 Feb;64(2):259-266
pubmed: 27681956
Oncotarget. 2018 Feb 12;9(18):14228-14250
pubmed: 29581840
Oncotarget. 2016 Jul 26;7(30):48375-48390
pubmed: 27356743
Eur J Nucl Med Mol Imaging. 2012 Jul;39(7):1097-106
pubmed: 22532252
J Natl Cancer Inst. 1977 May;58(5):1267-70
pubmed: 853525
Radiat Oncol. 2019 Jan 17;14(1):9
pubmed: 30654815
J Clin Oncol. 2017 Feb 10;35(5):498-505
pubmed: 27918720
Onco Targets Ther. 2016 Jan 05;9:159-70
pubmed: 26793000
Int J Radiat Oncol Biol Phys. 2015 Apr 1;91(5):952-60
pubmed: 25832687
Control Clin Trials. 1996 Aug;17(4):343-6
pubmed: 8889347
J Clin Oncol. 2000 Oct 1;18(19):3339-45
pubmed: 11013273
Int J Cancer. 2017 May 15;140(10):2256-2264
pubmed: 28224615
PLoS One. 2011;6(7):e22039
pubmed: 21760951
Cancer. 2011 Jan 1;117(1):197-206
pubmed: 20737561
Front Oncol. 2018 Dec 19;8:597
pubmed: 30619740
Oral Oncol. 2015 Nov;51(11):1041-1046
pubmed: 26296274
Pediatr Blood Cancer. 2010 Aug;55(2):279-84
pubmed: 20582982
Ann Oncol. 2015 Jan;26(1):205-211
pubmed: 25355717
Cancer. 2005 Sep 1;104(5):1083-9
pubmed: 15999363
Eur J Cancer. 2015 Aug;51(12):1570-9
pubmed: 26044925
J Clin Oncol. 2017 Dec 20;35(36):4050-4056
pubmed: 28837405
Lancet Oncol. 2015 Jun;16(6):645-55
pubmed: 25957714
J Pediatr Hematol Oncol. 2018 Mar;40(2):85-92
pubmed: 29300240
Radiat Oncol. 2015 Mar 26;10:70
pubmed: 25889937
Cancer Res Treat. 2018 Oct;50(4):1304-1315
pubmed: 29334605
J Cancer. 2011;2:341-6
pubmed: 21716854
Eur J Cancer. 2019 Mar;110:24-31
pubmed: 30739837
Mol Ther. 2014 Jan;22(1):132-9
pubmed: 24297049
Ann Oncol. 2018 Mar 1;29(3):731-736
pubmed: 29236943
Cancer. 2005 Feb 15;103(4):850-7
pubmed: 15641027
J Pediatr Hematol Oncol. 2017 Nov;39(8):e437-e442
pubmed: 28816803
Ann Oncol. 2018 Sep 1;29(9):1972-1979
pubmed: 30016391