Literature DB >> 26459257

Is c-Met oncoprotein expression an adverse prognosticator in extrahepatic bile duct cancer treated with curative resection followed by adjuvant chemoradiotherapy?

H J Park1, K Kim2, J H Paik3, E K Chie4,5, S Kim4, J-Y Jang6, S W Kim6, S-W Han7, D-Y Oh7, S-A Im7, T-Y Kim7, Y-J Bang7, S W Ha4,5.   

Abstract

PURPOSE: To analyze the expression of c-Met, and to investigate correlations between the expression of c-Met, clinicopathologic variables, and survival in patients undergoing curative surgery followed by adjuvant chemoradiotherapy for extrahepatic bile duct (EHBD) cancer.
METHODS: Ninety EHBD cancer patients who underwent curative resection followed by adjuvant chemoradiotherapy were enrolled. Expression of c-Met was assessed with immunohistochemical staining on tissue microarray. The correlation between clinicopathologic variables and survival outcomes was evaluated using Kaplan-Meier method and Cox proportional hazard model.
RESULTS: On univariate analysis, 66 patients (76.7 %) showed c-Met expression. c-Met expression had a significant impact on 5-year overall survival (OS) (43.0 % in c-Met(+) vs. 25.0 % in c-Met(-), p = 0.0324), but not on loco-regional relapse-free survival or distant metastasis-free survival (DMFS). However, on multivariate analysis incorporating tumor location and nodal involvement, survival difference was not maintained (p = 0.2940). Tumor location was the only independent prognostic factor predicting OS (p = 0.0089). Hilar location tumors, nodal involvement, and poorly differentiated tumors were all identified as independent prognostic factors predicting inferior DMFS (p = 0.0030, 0.0013, and 0.0037, respectively).
CONCLUSIONS: This study showed that c-Met expression was not associated with survival outcomes in EHBD cancer patients undergoing curative resection followed by adjuvant chemoradiotherapy. Further studies are needed to fully elucidate the prognostic value of c-Met expression in these patients.

Entities:  

Keywords:  Adjuvant chemoradiotherapy; Extrahepatic bile duct cancer; c-Met

Mesh:

Substances:

Year:  2015        PMID: 26459257     DOI: 10.1007/s12094-015-1409-5

Source DB:  PubMed          Journal:  Clin Transl Oncol        ISSN: 1699-048X            Impact factor:   3.405


  23 in total

1.  The HGF receptor c-Met is overexpressed in esophageal adenocarcinoma.

Authors:  Luis J Herrera; Talal El-Hefnawy; Pierre E Queiroz de Oliveira; Siva Raja; Sydney Finkelstein; William Gooding; James D Luketich; Tony E Godfrey; Steven J Hughes
Journal:  Neoplasia       Date:  2005-01       Impact factor: 5.715

2.  Amplification and overexpression of c-erbB-2, epidermal growth factor receptor, and c-met in biliary tract cancers.

Authors:  Kumiko Nakazawa; Yoh Dobashi; Shioto Suzuki; Hideki Fujii; Yasuhisa Takeda; Akishi Ooi
Journal:  J Pathol       Date:  2005-07       Impact factor: 7.996

3.  c-erbB-2 and c-Met expression relates to cholangiocarcinogenesis and progression of intrahepatic cholangiocarcinoma.

Authors:  S-I Aishima; K-I Taguchi; K Sugimachi; M Shimada; K Sugimachi; M Tsuneyoshi
Journal:  Histopathology       Date:  2002-03       Impact factor: 5.087

4.  The expression of phospho-AKT, phospho-mTOR, and PTEN in extrahepatic cholangiocarcinoma.

Authors:  Joon-Yong Chung; Seung-Mo Hong; Byeong Yeob Choi; Hyungjun Cho; Eunsil Yu; Stephen M Hewitt
Journal:  Clin Cancer Res       Date:  2009-01-15       Impact factor: 12.531

5.  ERBB-2 overexpression and cyclooxygenase-2 up-regulation in human cholangiocarcinoma and risk conditions.

Authors:  Kanenori Endo; Byung-Il Yoon; Chawalit Pairojkul; Anthony J Demetris; Alphonse E Sirica
Journal:  Hepatology       Date:  2002-08       Impact factor: 17.425

Review 6.  c-Met targeted therapy of cholangiocarcinoma.

Authors:  Matei-P Socoteanu; Frank Mott; Gianfranco Alpini; Arthur-E Frankel
Journal:  World J Gastroenterol       Date:  2008-05-21       Impact factor: 5.742

7.  The overexpression of c-met as a prognostic indicator for gastric carcinoma compared to p53 and p21 nuclear accumulation.

Authors:  Uta Drebber; Stephan E Baldus; Britt Nolden; Guido Grass; Elfriede Bollschweiler; Hans P Dienes; Arnulf H Hölscher; Stefan P Mönig
Journal:  Oncol Rep       Date:  2008-06       Impact factor: 3.906

Review 8.  Novel therapeutic inhibitors of the c-Met signaling pathway in cancer.

Authors:  Joseph Paul Eder; George F Vande Woude; Scott A Boerner; Patricia M LoRusso
Journal:  Clin Cancer Res       Date:  2009-03-24       Impact factor: 12.531

9.  Overexpression of c-met proto-oncogene but not epidermal growth factor receptor or c-erbB-2 in primary human colorectal carcinomas.

Authors:  C Liu; M Park; M S Tsao
Journal:  Oncogene       Date:  1992-01       Impact factor: 9.867

10.  Molecular biomarkers in extrahepatic bile duct cancer patients undergoing chemoradiotherapy for gross residual disease after surgery.

Authors:  Hyeon Kang Koh; Hae Jin Park; Kyubo Kim; Eui Kyu Chie; Hye Sook Min; Sung W Ha
Journal:  Radiat Oncol J       Date:  2012-12-31
View more
  2 in total

1.  PF-2341066 combined with celecoxib promotes apoptosis and inhibits proliferation in human cholangiocarcinoma QBC939 cells.

Authors:  Chen Chen; Dinghua Yang; Qinghua Zeng; Liang Luo; Chengzhi Cai
Journal:  Exp Ther Med       Date:  2018-03-20       Impact factor: 2.447

2.  The Clinical Impact of c-MET Over-Expression in Advanced Biliary Tract Cancer (BTC).

Authors:  Mi Hwa Heo; Hee Kyung Kim; Hansang Lee; Kyoung-Mee Kim; Jeeyun Lee; Se Hoon Park; Joon Oh Park; Ho Yeong Lim; Won Ki Kang; Young Suk Park; Seung Tae Kim
Journal:  J Cancer       Date:  2017-05-12       Impact factor: 4.207

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.