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)

Author:

Ferris Robert L.1ORCID,Flamand Yael2,Weinstein Gregory S.3,Li Shuli2,Quon Harry4ORCID,Mehra Ranee5ORCID,Garcia Joaquin J.6,Chung Christine H.7ORCID,Gillison Maura L.8,Duvvuri Umamaheswar1,O'Malley Bert W.3,Ozer Enver9,Thomas Giovana R.10,Koch Wayne M.4,Gross Neil D.8ORCID,Bell R. Bryan11ORCID,Saba Nabil F.12ORCID,Lango Miriam13ORCID,Méndez Eduardo1415,Burtness Barbara16ORCID

Affiliation:

1. UPMC Hillman Cancer Center, Pittsburgh, PA

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

3. University of Pennsylvania, Philadelphia, PA

4. Johns Hopkins University, Baltimore, MD

5. University of Maryland, Baltimore, MD

6. Mayo Clinic, Rochester, MN

7. Moffitt Cancer Center, Tampa FL

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

9. The Ohio State University, Columbus, OH

10. University of Miami, Miami, FL

11. Providence Cancer Institute, Portland, OR

12. Winship Cancer Institute at Emory University, Atlanta, GA

13. Fox Chase Cancer Center, Philadelphia, PA

14. University of Washington, Seattle, WA

15. Deceased.

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

Abstract

PURPOSE 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. METHODS 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. RESULTS 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. CONCLUSION Primary TOS and reduced postoperative RT result in outstanding oncologic outcome and favorable functional outcomes in intermediate-risk HPV+ OPC.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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