Pathologic and Prognostic Implications of Incidental versus Nonincidental Gallbladder Cancer: A 10-Institution Study from the United States Extrahepatic Biliary Malignancy Consortium

Author:

Ethun Cecilia G.1,Le Nina1,Lopez-Aguiar Alexandra G.1,Pawlik Timothy M.23,Poultsides George4,Tran Thuy4,Idrees Kamran5,Isom Chelsea A.5,Fields Ryan C.6,Krasnick Bradley A.6,Weber Sharon M.7,Salem Ahmed7,Martin Robert C. G.8,Scoggins Charles R.8,Shen Perry9,Mogal Harveshp D.9,Schmidt Carl3,Beal Eliza3,Hatzaras Ioannis10,Shenoy Rivfka10,Russell Maria C.1,Maithel Shishir K.1

Affiliation:

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

2. Division of Surgical Oncology, Department of Surgery, The Johns Hopkins Hospital, Baltimore, Maryland;

3. Division of Surgical Oncology, The Ohio State University, Columbus, Ohio;

4. Department of Surgery, Stanford University Medical Center, Stanford, California;

5. Division of Surgical Oncology, Department of Surgery, Vanderbilt University, Nashville, Tennessee;

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

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

8. Division of Surgical Oncology, Department of Surgery, University of Louisville, Louisville, Kentucky;

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

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

Abstract

Most gallbladder cancers (GBCs) are discovered incidentally after routine cholecystectomy. The influence of timing of diagnosis on disease stage, treatment, and prognosis is not known. Patients with GBC who underwent resection at 10 institutions from 2000 to 2015 were included. Patients diagnosed incidentally (IGBC) and nonincidentally (non-IGBC) were compared. Primary outcome was overall survival (OS). Of 445 patients with GBC, 266 (60%) were IGBC and 179 (40%) were non-IGBC. Compared with IGBC, non-IGBC patients were more likely to have R2 resections (43% vs 19%; P < 0.001), advanced T-stage (T3/T4: 70% vs 40%; P < 0.001), high-grade tumors (50% vs 31%; P < 0.001), lymphovascular invasion (64% vs 45%; P = 0.01), and positive lymph nodes (60% vs 43%; P = 0.009). Receipt of adjuvant chemotherapy was similar between groups (49% vs 49%). Non-IGBC was associated with worse median OS compared with IGBC (17 vs 32 months; P < 0.001), which persisted among stage III patients (12 vs 29 months; P < 0.001), but not stages I, II, or IV. Despite accounting for other adverse pathologic factors (grade, T-stage, lymphovascular invasion, margin, lymph node), adjuvant chemotherapy was associated with improved OS only in stage III IGBC, but not in non-IGBC. Compared with incidental discovery, non-IGBC is associated with reduced OS, which is most evident in stage III disease. Despite being well matched for other adverse pathologic factors, adjuvant chemotherapy was associated with improved survival only in stage III patients with incidentally discovered cancer. This underscores the importance of timing of diagnosis in GBC and suggests that these two groups may represent a distinct biology of disease, and the same treatment paradigm may not be appropriate.

Publisher

SAGE Publications

Subject

General Medicine

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