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Metabolic Characteristics of Advanced Biliary Tract Cancer Using 18F‐Fluorodeoxyglucose Positron Emission Tomography and Their Clinical Implications
Authors:Kyoung‐Min Cho  Do‐Youn Oh  Tae‐Yong Kim  Kyung Hun Lee  Sae‐Won Han  Seock‐Ah Im  Tae‐You Kim  Yung‐Jue Bang
Affiliation:1. Department of Internal Medicine, Seoul National University Hospital, Seoul, Republic of Korea;2. Cancer Research Institute, Seoul National University College of Medicine, Seoul, Republic of Korea
Abstract:

Background.

In advanced biliary tract cancer (BTC), the metabolic landscape has not been evaluated by 18F-fluorodeoxyglucose (FDG) positron emission tomography (PET) yet. Furthermore, reports of the clinical implications of these metabolic features are limited. We aimed to evaluate the metabolic features and their clinical relevance in advanced BTC using 18F-FDG PET.

Patients and Methods.

We consecutively enrolled patients with advanced BTC who underwent 18F-FDG PET prior to palliative chemotherapy between 2003 and 2013. We evaluated the findings of PET, such as SUVmax, the number of lesions and organs with FDG uptake, pathologic findings, and clinical outcomes.

Results.

A total of 106 patients were enrolled: (53 intrahepatic cholangiocarcinoma ICC], 7 extrahepatic BTC, 30 gallbladder cancer GB Ca], and 16 ampulla of Vater cancer AoV Ca]). The median SUVmax differed according to the primary origin (ICC, 9.10; extrahepatic BTC, 5.90; GB Ca, 9.10; and AoV Ca, 6.37; p = .008) and histologic differentiation (well differentiated, 4.95; moderately differentiated, 6.60; poorly differentiated, 14.50; p = .004). Patients in the high metabolic group (SUVmax of ≥7.5) had more poorly differentiated histology and more organs and lesions with FDG uptake than did those in the low metabolic group (SUVmax of <7.5). The low metabolic group had a significantly longer OS (11.4 vs. 7.4 months, p = .007) and PFS (6.6 vs. 4.3 months, p = .024) than high metabolic group. In multivariate analysis, SUVmax was a significant prognostic factor for overall survival (OS; p = .047) and progression-free survival (PFS; p = .039).

Conclusion.

Metabolic characteristics of advanced BTC differ according to primary origin and histology. These metabolic features could be prognostic factors for OS and PFS in advanced BTC.

Implications for Practice:

The metabolic landscape of advanced biliary tract cancer and its clinical meanings have not yet been comprehensively studied. This study shows that metabolic characteristics of advanced biliary tract cancer differ significantly according to primary origin and histology. Moreover, this metabolic activity is associated with patients’ outcomes, including overall survival and progression-free survival. This study supports tumor heterogeneity in terms of cancer metabolism in biliary tract cancer.
Keywords:Advanced biliary tract cancer  Metabolism  Prognosis  Positron emission tomography  Standardized uptake value
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