Identification of patients who may benefit the most from adjuvant chemotherapy following resection of incidental gallbladder carcinoma.


Journal

Journal of surgical oncology
ISSN: 1096-9098
Titre abrégé: J Surg Oncol
Pays: United States
ID NLM: 0222643

Informations de publication

Date de publication:
Mar 2021
Historique:
received: 14 10 2020
revised: 23 12 2020
accepted: 10 01 2021
pubmed: 27 1 2021
medline: 11 3 2021
entrez: 26 1 2021
Statut: ppublish

Résumé

To develop a scoring system to identify the subset of patients who may benefit the most from adjuvant chemotherapy following curative-intent resection for incidental gallbladder cancer (IGBC). A novel scoring system was utilized to stratify patients relative to overall survival (OS), as well as potential benefit from adjuvant chemotherapy following curative resection for IGBC. Among 266 patients with IGBC, a total of 99 (37.2%) patients received adjuvant chemotherapy. Five risk factors were used to develop an integer-based score to predict OS. Risk of death at 5-years incrementally increased among patients in the low (n = 42, 69.0%), medium (n = 64, 56.3%) and high-risk groups (n = 40, 30.0%) (median OS, 99.4 vs. 33.5 vs. 15.6 months, all p < .001). Use of adjuvant chemotherapy did not provide a survival benefit among patients in the low-risk group (median survival, 99.4 vs. 60.7 months, p = .56). In contrast, utilization of adjuvant chemotherapy was associated with an improvement in survival among medium- (median survival, 21.7 vs. 59.5 months, p = .04) and high-risk patients (median survival, 11.6 vs. 20.1 months, p = .01). While low-risk patients did not benefit from adjuvant chemotherapy, individuals with medium or high-risk scores had an improved survival with the utilization of adjuvant chemotherapy.

Sections du résumé

BACKGROUND BACKGROUND
To develop a scoring system to identify the subset of patients who may benefit the most from adjuvant chemotherapy following curative-intent resection for incidental gallbladder cancer (IGBC).
METHODS METHODS
A novel scoring system was utilized to stratify patients relative to overall survival (OS), as well as potential benefit from adjuvant chemotherapy following curative resection for IGBC.
RESULTS RESULTS
Among 266 patients with IGBC, a total of 99 (37.2%) patients received adjuvant chemotherapy. Five risk factors were used to develop an integer-based score to predict OS. Risk of death at 5-years incrementally increased among patients in the low (n = 42, 69.0%), medium (n = 64, 56.3%) and high-risk groups (n = 40, 30.0%) (median OS, 99.4 vs. 33.5 vs. 15.6 months, all p < .001). Use of adjuvant chemotherapy did not provide a survival benefit among patients in the low-risk group (median survival, 99.4 vs. 60.7 months, p = .56). In contrast, utilization of adjuvant chemotherapy was associated with an improvement in survival among medium- (median survival, 21.7 vs. 59.5 months, p = .04) and high-risk patients (median survival, 11.6 vs. 20.1 months, p = .01).
CONCLUSIONS CONCLUSIONS
While low-risk patients did not benefit from adjuvant chemotherapy, individuals with medium or high-risk scores had an improved survival with the utilization of adjuvant chemotherapy.

Identifiants

pubmed: 33497466
doi: 10.1002/jso.26389
doi:

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

978-985

Informations de copyright

© 2021 Wiley Periodicals LLC.

Références

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Auteurs

Jun-Xi Xiang (JX)

Department of Hepatobiliary Surgery, Institute of Advanced Surgical Technology and Engineering, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, China.

Xu-Feng Zhang (XF)

Department of Hepatobiliary Surgery, Institute of Advanced Surgical Technology and Engineering, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, China.
Department of Surgery, Wexner Medical Center, The Ohio State University, Columbus, Ohio, USA.

Sharon M Weber (SM)

Department of Surgery, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin, USA.

George Poultsides (G)

Department of Surgery, Stanford University Medical Center, Stanford, California, USA.

Ryan C Fields (RC)

Department of Surgery, Washington University School of Medicine, St Louis, Missouri, USA.

Ioannis Hatzaras (I)

Department of Surgery, New York University, New York, New York, USA.

Matthew Weiss (M)

Department of Surgery, Northwell Health Cancer Institute, Zucker School of Medicine at Hofstra, Lake Success, New York, USA.

Charles Scoggins (C)

Division of Surgical Oncology, Department of Surgery, Winship Cancer Institute, Emory University, Atlanta, Georgia, USA.

Kamron Idrees (K)

Division of Surgical Oncology, Department of Surgery, University of Louisville, Louisville, Kentucky, USA.

Perry Shen (P)

Department of Surgery, Wake Forest University, Winston-Salem, North Carolina, USA.

Shishir K Maithel (SK)

Division of Surgical Oncology, Department of Surgery, Vanderbilt University Medical Center, Nashville, Tennessee, USA.

Timothy M Pawlik (TM)

Department of Surgery, Wexner Medical Center, The Ohio State University, Columbus, Ohio, USA.

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