Back to Search Start Over

Reduced-Dose Radiation Therapy for HPV-Associated Oropharyngeal Carcinoma (NRG Oncology HN002).

Authors :
Yom, Sue S
Yom, Sue S
Torres-Saavedra, Pedro
Caudell, Jimmy J
Waldron, John N
Gillison, Maura L
Xia, Ping
Truong, Minh T
Kong, Christina
Jordan, Richard
Subramaniam, Rathan M
Yao, Min
Chung, Christine H
Geiger, Jessica L
Chan, Jason W
O'Sullivan, Brian
Blakaj, Dukagjin M
Mell, Loren K
Thorstad, Wade L
Jones, Christopher U
Banerjee, Robyn N
Lominska, Christopher
Le, Quynh-Thu
Yom, Sue S
Yom, Sue S
Torres-Saavedra, Pedro
Caudell, Jimmy J
Waldron, John N
Gillison, Maura L
Xia, Ping
Truong, Minh T
Kong, Christina
Jordan, Richard
Subramaniam, Rathan M
Yao, Min
Chung, Christine H
Geiger, Jessica L
Chan, Jason W
O'Sullivan, Brian
Blakaj, Dukagjin M
Mell, Loren K
Thorstad, Wade L
Jones, Christopher U
Banerjee, Robyn N
Lominska, Christopher
Le, Quynh-Thu
Source :
Journal of clinical oncology : official journal of the American Society of Clinical Oncology; vol 39, iss 9, 956-965; 0732-183X
Publication Year :
2021

Abstract

PurposeReducing radiation treatment dose could improve the quality of life (QOL) of patients with good-risk human papillomavirus-associated oropharyngeal squamous cell carcinoma (OPSCC). Whether reduced-dose radiation produces disease control and QOL equivalent to standard chemoradiation is not proven.Patients and methodsIn this randomized, phase II trial, patients with p16-positive, T1-T2 N1-N2b M0, or T3 N0-N2b M0 OPSCC (7th edition staging) with ≤ 10 pack-years of smoking received 60 Gy of intensity-modulated radiation therapy (IMRT) over 6 weeks with concurrent weekly cisplatin (C) or 60 Gy IMRT over 5 weeks. To be considered for a phase III study, an arm had to achieve a 2-year progression-free survival (PFS) rate superior to a historical control rate of 85% and a 1-year mean composite score ≥ 60 on the MD Anderson Dysphagia Inventory (MDADI).ResultsThree hundred six patients were randomly assigned and eligible. Two-year PFS for IMRT + C was 90.5% rejecting the null hypothesis of 2-year PFS ≤ 85% (P = .04). For IMRT, 2-year PFS was 87.6% (P = .23). One-year MDADI mean scores were 85.30 and 81.76 for IMRT + C and IMRT, respectively. Two-year overall survival rates were 96.7% for IMRT + C and 97.3% for IMRT. Acute adverse events (AEs) were defined as those occurring within 180 days from the end of treatment. There were more grade 3-4 acute AEs for IMRT + C (79.6% v 52.4%; P < .001). Rates of grade 3-4 late AEs were 21.3% and 18.1% (P = .56).ConclusionThe IMRT + C arm met both prespecified end points justifying advancement to a phase III study. Higher rates of grade ≥ 3 acute AEs were reported in the IMRT + C arm.

Details

Database :
OAIster
Journal :
Journal of clinical oncology : official journal of the American Society of Clinical Oncology; vol 39, iss 9, 956-965; 0732-183X
Notes :
application/pdf, Journal of clinical oncology : official journal of the American Society of Clinical Oncology vol 39, iss 9, 956-965 0732-183X
Publication Type :
Electronic Resource
Accession number :
edsoai.on1367471669
Document Type :
Electronic Resource