A novel surgeon credentialing and quality assurance process using transoral surgery for oropharyngeal cancer in ECOG-ACRIN Cancer Research Group Trial E3311
Name:
Publisher version
View Source
Access full-text PDFOpen Access
View Source
Check access options
Check access options
Author
Ferris, Robert L.Flamand, Yael
Holsinger, F. Christopher
Weinstein, Gregory S.
Quon, Harry
Mehra, Ranee
Garcia, Joaquin J.
Hinni, Michael L.
Gross, Neil D.
Sturgis, Erich M.
Duvvuri, Umamaheswar
Méndez, Eduardo
Ridge, John A.
Magnuson, J. Scott
Higgins, Kerry A.
Patel, Mihir R.
Smith, Russel B.
Karakla, Daniel W.
Kupferman, Michael E.
Malone, James P.
Judson, Benjamin L.
Richmon, Jeremy
Boyle, Jay O.
Bayon, Rodrigo
O'Malley, Bert W.
Ozer, Enver
Thomas, Giovana R.
Koch, Wayne M.
Bell, R. Bryan
Saba, Nabil F.
Li, Shuli
Sigurdson, Elin R.
Burtness, Barbara
Date
2020-11Journal
Oral OncologyPublisher
Elsevier BVType
Article
Metadata
Show full item recordAbstract
Purpose: Understanding the role of transoral surgery in oropharyngeal cancer (OPC) requires prospective, randomized multi-institutional data. Meticulous evaluation of surgeon expertise and surgical quality assurance (QA) will be critical to the validity of such trials. We describe a novel surgeon credentialing and QA process developed to support the ECOG-ACRIN Cancer Research Group E3311 (E3311) and report outcomes related to QA. Patients and methods: E3311 was a phase II randomized clinical trial of transoral surgery followed by low- or standard-dose, risk-adjusted post-operative therapy with stage III-IVa (AJCC 7th edition) HPV-associated OPC. In order to be credentialed to accrue to this trial, surgeons were required to demonstrate active hospital credentials and technique-specific surgical expertise with ≥20 cases of transoral resection for OPC. In addition, 10 paired operative and surgical pathology reports from the preceding 24 months were reviewed by an expert panel. Ongoing QA required <10% rate of positive margins, low oropharyngeal bleeding rates, and accrual of at least one patient per 12 months. Otherwise surgeons were placed on hold and not permitted to accrue until re-credentialed using a new series of transoral resections. Results: 120 surgeons trained in transoral minimally invasive surgery applied for credentialing for E3311 and after peer-review, 87 (73%) were approved from 59 centers. During QA on E3311, positive final pathologic margins were reported in 19 (3.8%) patients. Grade III/IV and grade V oropharyngeal bleeding was reported in 29 (5.9%) and 1 (0.2%) of patients. Conclusions: We provide proof of concept that a comprehensive credentialing process can support multicenter transoral head and neck surgical oncology trials, with low incidence of positive margins and *grade III/V oropharyngeal bleeding. Copyright 2020 The Authors.Rights/Terms
© 2020 The Authors. Published by Elsevier Ltd.Identifier to cite or link to this item
http://hdl.handle.net/10713/13399ae974a485f413a2113503eed53cd6c53
10.1016/j.oraloncology.2020.104797