CS-iCCA, A New Clinically Based Staging System for Intrahepatic Cholangiocarcinoma: Establishment and External Validation

Author:

Lozada Maria E.12,Zhang Ning13,Jin Weidong14,Wongjarupong Nicha15,Yang Ju Dong16,Voss Molly M.7,Prasai Kritika1,Amakye Dominic O.18ORCID,Harmsen William S.7,Chaudhary Sushant9,Bathe Oliver F.9,Borad Mitesh J.10,Patel Tushar C.11,Gores Gregory J.1,Therneau Terry M.7,Roberts Lewis R.1

Affiliation:

1. Division of Gastroenterology and Hepatology, Mayo Clinic College of Medicine and Science, Rochester, Minnesota, USA;

2. Department of Surgery, University of Puerto Rico School of Medicine, San Juan, Puerto Rico, USA;

3. Integrated TCM & Western Medicine Department, the Fifth Medical Center, Chinese PLA General Hospital, Beijing, China;

4. Department of General Surgery, Wuhan General Hospital of Guangzhou Military, Wuhan, China;

5. Department of Medicine, University of Minnesota School of Medicine, Minneapolis, Minnesota, USA;

6. Division of Digestive and Liver Diseases, Department of Internal Medicine, Comprehensive Transplant Center, and Samuel Oschin Comprehensive Cancer Institute, Cedars-Sinai Medical Center, Los Angeles, California, USA;

7. Division of Biomedical Statistics and Informatics, Mayo Clinic College of Medicine and Science, Rochester, Minnesota, USA;

8. Department of Internal Medicine, Piedmont Athens Regional Medical Center, Athens, Georgia, USA;

9. Departments of Surgery and Oncology, University of Calgary, Calgary, Alberta, Canada;

10. Division of Hematology and Medical Oncology, Mayo Clinic Hospital, Phoenix, Arizona, USA;

11. Department of Transplantation and Division of Gastroenterology and Hepatology, Mayo Clinic, Jacksonville, Florida, USA.

Abstract

INTRODUCTION: Intrahepatic cholangiocarcinoma (iCCA) is a primary liver malignancy with poor prognosis. Current prognostic methods are most accurate for patients with surgically resectable disease. However, a significant proportion of patients with iCCA are not surgical candidates. We aimed to develop a generalizable staging system based on clinical variables to determine prognosis of all patients with iCCA. METHODS: The derivation cohort included 436 patients with iCCA seen between 2000 and 2011. For external validation, 249 patients with iCCA seen from 2000 to 2014 were enrolled. Survival analysis was performed to identify prognostic predictors. All-cause mortality was the primary end point. RESULTS: Eastern Cooperative Oncology Group status, tumor number, tumor size, metastasis, albumin, and carbohydrate antigen 19-9 were incorporated into a 4-stage algorithm. Kaplan-Meier estimates for 1-year survival were 87.1% (95% confidence interval [CI] 76.1–99.7), 72.7% (95% CI 63.4–83.4), 48.0% (95% CI 41.2–56.0), and 16% (95% CI 11–23.5), respectively, for stages I, II, III, and IV. Univariate analysis yielded significant differences in risk of death for stages II (hazard ratio [HR] 1.71; 95% CI 1.0–2.8), III (HR 3.32; 95% CI 2.07–5.31), and IV (HR 7.44; 95% CI 4.61–12.01) compared with stage I (reference). Concordance indices showed the new staging system was superior to the TNM staging for predicting mortality in the derivation cohort, P < 0.0001. In the validation cohort, however, the difference between the 2 staging systems was not significant. DISCUSSION: The proposed independently validated staging system uses nonhistopathologic data to successfully stratify patients into 4 stages. This staging system has better prognostic accuracy compared with the TNM staging and can assist physicians and patients in treatment of iCCA.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Gastroenterology,Hepatology

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