Publication

Adjuvant therapy following resection of gastroenteropancreatic neuroendocrine tumors provides no recurrence or survival benefit

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Last modified
  • 05/21/2025
Type of Material
Authors
    James R. Barrett, University of Wisconsin-MadisonVictoria Rendell, University of Wisconsin-MadisonCourtney Pokrzywa, University of Wisconsin-MadisonAlexandra G. Lopez-Aguiar, Emory UniversityJohn Cannon, Stanford UniversityGeorge A. Poultsides, Stanford UniversityFlavio Rocha, Virginia Mason Medical CenterAngelena Crown, Virginia Mason Medical CenterEliza Beal, Ohio State UniversityTimothy Michael Pawlik, Ohio State UniversityRyan Fields, Washington University St. LouisRoheena Z. Panni, Washington University St. LouisPaula Smith, Vanderbilt UniversityKamran Idrees, Vanderbilt UniversityClifford Cho, University of MichiganMegan Beems, University of MichiganShishir Maithel, Emory UniversitySharon Weber, University of Wisconsin-MadisonDaniel Erik Abbott, University of Wisconsin-Madison
Language
  • English
Date
  • 2020-06-01
Publisher
  • John Wiley & Sons, Inc.
Publication Version
Copyright Statement
  • © 2020 Wiley Periodicals, Inc.
Final Published Version (URL)
Title of Journal or Parent Work
Volume
  • 121
Issue
  • 7
Start Page
  • 1067
End Page
  • 1073
Grant/Funding Information
  • Research reported in this publication was supported by the National Cancer Institute of the National Institutes of Health under Award Number T32CA090217. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health.
Abstract
  • Background and Objectives Lack of high-level evidence supporting adjuvant therapy for patients with resected gastroenteropancreatic neuroendocrine tumors (GEP NETs) warrants an evaluation of its non-standard of care use. Methods Patients with primary GEP NETs who underwent curative-intent resection at eight institutions between 2000 and 2016 were identified; 91 patients received adjuvant therapy. Recurrence-free survival (RFS) and overall survival (OS) were compared between adjuvant cytotoxic chemotherapy and somatostatin analog cohorts. Results In resected patients, 33 received cytotoxic chemotherapy, and 58 received somatostatin analogs. Five-year RFS/OS was 49% and 83%, respectively. Cytotoxic chemotherapy RFS/OS was 36% and 61%, respectively, lower than the no therapy cohort (P <.01). RFS with somatostatin analog therapy (compared to none) was lower (P <.01), as was OS (P =.01). On multivariable analysis, adjuvant cytotoxic therapy was negatively associated with RFS but not OS controlling for patient/tumor-specific characteristics (RFS P <.01). Conclusions Our data, reflecting the largest reported experience to date, demonstrate that adjuvant therapy for resected GEP NETs is negatively associated with RFS and confers no OS benefit. Selection bias enriching our treatment cohort for individuals with unmeasured high-risk characteristics likely explains some of these results; future studies should focus on patient subsets who may benefit from adjuvant therapy.
Author Notes
  • Corresponding Author: James R Barrett, MD: 600 Highland Avenue, Madison, WI, 53792. Phone: 001 (608) 262-9134, jbarrett2@uwhealth.org
Keywords
Research Categories
  • Health Sciences, Oncology
  • Health Sciences, Rehabilitation and Therapy

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