4.4 Article

Chromosomal aberrations, visualized using UroVysion® fluorescence in-situ hybridization assay, can predict poor prognosis in formalin-fixed paraffin-embedded tissues of cholangiocarcinoma patients

Journal

HUMAN PATHOLOGY
Volume 126, Issue -, Pages 31-44

Publisher

W B SAUNDERS CO-ELSEVIER INC
DOI: 10.1016/j.humpath.2022.05.008

Keywords

Cholangiocarcinoma; Chromosomal aberrations; UroVysion (R); Prognosis; Fluorescence in-situ hybridization

Categories

Funding

  1. NSRF through Cholangiocarcinoma Research Institute
  2. Faculty of Medicine, Khon Kaen University
  3. Faculty of Medicine, Khon KaenUniversity, Thailand [IN64143]

Ask authors/readers for more resources

This study investigates the association between chromosomal aberrations, clinical data, and overall survival time in patients with cholangiocarcinoma (CCA). The results show that polysomy of chromosomes 3 and 7 is significantly associated with shorter survival time, and the presence of polysomy of chromosomes 3, 7, and 17 along with heterozygous loss of 9p21 is associated with even shorter survival time. Multivariate analysis identifies polysomy of chromosomes 3 and 7, as well as polysomy of chromosomes 3, 7, and 17 with heterozygous loss of 9p21, as independent predictive factors of poor overall survival in CCA patients.
Cholangiocarcinoma (CCA) is a highly aggressive malignant tumor that has highest incidence in northeastern Thailand. The survival rate of CCA patients after receiving surgical treatment is quite low. Recently, genetic alterations including chromosome abnormalities have been studied as predictive factors and to aid planning for further treatment. This study aims to investigate the association between chromosomal aberrations, clinical data, and overall survival time of CCA patients. Formalin-fixed paraffin-embedded (FFPE) tissues from 194 CCA patients were examined. The copy numbers of chromosomes 3, 7, 17 and 9p21 were investigated using the UroVysion (R) fluorescence in-situ hybridization (FISH) assay. The overall survival time (OS) of CCA patients with or without polysomy of chromosomes 3, 7, 17 and/or loss of 9p21 were statistically analyzed in association with their clinicopathological parameters. KaplaneMeier analysis was performed. The OS of patients with polysomy of chromosomes 3 + 7 was significantly shorter than those without this polysomy (log-rank P = 0.006; median OS 14.79 vs. 19.62 months). Moreover, patients with polysomy of chromosomes 3 + 7+17 and heterozygous for 9p21 loss have significantly shorter survival time than those without such chromosomal aberrations (log-rank P = 0.001; median OS 15.74 vs. 37.57 months). Interestingly, multivariate analysis revealed that polysomy of chromosomes 3 + 7 and of chromosomes 3 + 7+17 with 9p21 heterozygous loss were independent predictive factors of a poor OS (P = 0.027; P = 0.008, respectively).The chromosomal aberrations patterns which we evaluated using FISH; 1) polysomy of chromosomes 3 + 7 and 2) polysomy of chromosomes 3 + 7+17 with 9p21 heterozygous loss, have strong potential as indicators of poor prognosis in CCA patients. (C) 2022 Published by Elsevier Inc.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.4
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available