Phase II Randomized Trial of Transoral Surgery and Low-Dose Intensity Modulated Radiation Therapy in Resectable p16+ Locally Advanced Oropharynx Cancer: An ECOG-ACRIN Cancer Research Group Trial (E3311).


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 01 2022
Historique:
pubmed: 27 10 2021
medline: 22 2 2022
entrez: 26 10 2021
Statut: ppublish

Résumé

Definitive or postoperative chemoradiation (CRT) is curative for human papillomavirus-associated (HPV+) oropharynx cancer (OPC) but induces significant toxicity. As a deintensification strategy, we studied primary transoral surgery (TOS) and reduced postoperative radiation therapy (RT) in intermediate-risk HPV+ OPC. E3311 is a phase II randomized trial of reduced- or standard-dose postoperative RT for resected stage III-IVa (American Joint Committee on Cancer-seventh edition) HPV+ OPC, determined by pathologic parameters. Primary goals were feasibility of prospective multi-institutional study of TOS for HPV+ OPC, and oncologic efficacy (2-year progression-free survival) of TOS and adjuvant therapy in intermediate-risk patients after resection. TOS plus 50 Gy was considered promising if the lower limit of the exact 90% binomial confidence intervals exceeded 85%. Quality of life and swallowing were measured by functional assessment of cancer therapy-head and neck and MD Anderson Dysphagia Index. Credentialed surgeons performed TOS for 495 patients. Eligible and treated patients were assigned as follows: arm A (low risk, n = 38) enrolled 11%, intermediate risk arms B (50 Gy, n = 100) or C (60 Gy, n = 108) randomly allocated 58%, and arm D (high risk, n = 113) enrolled 31%. With a median 35.2-month follow-up for 359 evaluable (eligible and treated) patients, 2-year progression-free survival Kaplan-Meier estimate is 96.9% (90% CI, 91.9 to 100) for arm A (observation), 94.9% (90% CI, 91.3 to 98.6]) for arm B (50 Gy), 96.0% (90% CI, 92.8 to 99.3) for arm C (60 Gy), and 90.7% (90% CI, 86.2 to 95.4) for arm D (66 Gy plus weekly cisplatin). Treatment arm distribution and oncologic outcome for ineligible or step 2 untreated patients (n = 136) mirrored the 359 evaluable patients. Exploratory comparison of functional assessment of cancer therapy-head and neck total scores between arms B and C is presented. Primary TOS and reduced postoperative RT result in outstanding oncologic outcome and favorable functional outcomes in intermediate-risk HPV+ OPC.

Identifiants

pubmed: 34699271
doi: 10.1200/JCO.21.01752
pmc: PMC8718241
doi:

Substances chimiques

Antineoplastic Agents 0
Biomarkers, Tumor 0
CDKN2A protein, human 0
Cyclin-Dependent Kinase Inhibitor p16 0
Cisplatin Q20Q21Q62J

Types de publication

Clinical Trial, Phase II Journal Article Multicenter Study Randomized Controlled Trial Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

138-149

Subventions

Organisme : NCI NIH HHS
ID : P30 CA016672
Pays : United States
Organisme : NCATS NIH HHS
ID : UL1 TR001863
Pays : United States
Organisme : NCI NIH HHS
ID : U24 CA196172
Pays : United States
Organisme : NCI NIH HHS
ID : U10 CA180820
Pays : United States
Organisme : NCI NIH HHS
ID : UG1 CA233247
Pays : United States
Organisme : NCI NIH HHS
ID : U10 CA180794
Pays : United States

Commentaires et corrections

Type : CommentIn
Type : CommentIn
Type : CommentIn
Type : CommentIn
Type : CommentIn
Type : CommentIn

Auteurs

Robert L Ferris (RL)

UPMC Hillman Cancer Center, Pittsburgh, PA.

Yael Flamand (Y)

Dana Farber Cancer Institute-ECOG-ACRIN Biostatistics Center, Boston, MA.

Gregory S Weinstein (GS)

University of Pennsylvania, Philadelphia, PA.

Shuli Li (S)

Dana Farber Cancer Institute-ECOG-ACRIN Biostatistics Center, Boston, MA.

Harry Quon (H)

Johns Hopkins University, Baltimore, MD.

Ranee Mehra (R)

University of Maryland, Baltimore, MD.

Joaquin J Garcia (JJ)

Mayo Clinic, Rochester, MN.

Christine H Chung (CH)

Moffitt Cancer Center, Tampa FL.

Maura L Gillison (ML)

The University of Texas, MD Anderson Cancer Center, Houston, TX.

Umamaheswar Duvvuri (U)

UPMC Hillman Cancer Center, Pittsburgh, PA.

Bert W O'Malley (BW)

University of Pennsylvania, Philadelphia, PA.

Enver Ozer (E)

The Ohio State University, Columbus, OH.

Giovana R Thomas (GR)

University of Miami, Miami, FL.

Wayne M Koch (WM)

Johns Hopkins University, Baltimore, MD.

Neil D Gross (ND)

The University of Texas, MD Anderson Cancer Center, Houston, TX.

R Bryan Bell (RB)

Providence Cancer Institute, Portland, OR.

Nabil F Saba (NF)

Winship Cancer Institute at Emory University, Atlanta, GA.

Miriam Lango (M)

Fox Chase Cancer Center, Philadelphia, PA.

Eduardo Méndez (E)

University of Washington, Seattle, WA.
Deceased.

Barbara Burtness (B)

Yale School of Medicine and Yale Cancer Center, New Haven, CT.

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Classifications MeSH