Genomic profiling of intrahepatic cholangiocarcinoma: refining prognosis and identifying therapeutic targets.

ABSTRACT:

Background

The molecular alterations that drive tumorigenesis in intrahepatic cholangiocarcinoma (ICC) remain poorly defined. We sought to determine the incidence and prognostic significance of mutations associated with ICC among patients undergoing surgical resection.

Methods

Multiplexed mutational profiling was performed using nucleic acids that were extracted from 200 resected ICC tumor specimens from 7 centers. The frequency of mutations was ascertained and the effect on outcome was determined.

Results

The majority of patients (61.5 %) had no genetic mutation identified. Among the 77 patients (38.5 %) with a genetic mutation, only a small number of gene mutations were identified with a frequency of >5 %: IDH1 (15.5 %) and KRAS (8.6 %). Other genetic mutations were

SUBMITTER: Zhu AX 

PROVIDER: S-EPMC4324507 | biostudies-literature | 2014 Nov

REPOSITORIES: biostudies-literature