A novel pretherapeutic gene expression-based risk score for treatment guidance in gastric cancer

Background - Perioperative chemotherapy is an established treatment of advanced gastric cancer patients. Treatment selection is based on clinical staging (cT). We aimed to establish and validate a prognostic score including clinical and molecular factors, to optimize treatment decisions for these pa...

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Main Authors: Bauer, Lukas (Author) , Blank, Susanne (Author) , Schmidt, Thomas (Author) , Weichert, Wilko (Author)
Format: Article (Journal)
Language:English
Published: 2018
In: Annals of oncology
Year: 2018, Volume: 29, Issue: 1, Pages: 127-132
ISSN:1569-8041
DOI:10.1093/annonc/mdx685
Online Access:Verlag, Volltext: https://doi.org/10.1093/annonc/mdx685
Verlag: http://www.sciencedirect.com/science/article/pii/S0923753419350057
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Author Notes:L. Bauer, A. Hapfelmeier, S. Blank, M. Reiche, J. Slotta-Huspenina, M. Jesinghaus, A. Novotny, T. Schmidt, B. Grosser, M. Kohlruss, W. Weichert, K. Ott & G. Keller

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520 |a Background - Perioperative chemotherapy is an established treatment of advanced gastric cancer patients. Treatment selection is based on clinical staging (cT). We aimed to establish and validate a prognostic score including clinical and molecular factors, to optimize treatment decisions for these patients. - Patients and methods - We analyzed 626 carcinomas of the stomach and of the gastro-esophageal junction from two academic centers including primarily resected and pre-/perioperatively treated patients. Patients were divided into a training (N = 269) and validation (N = 357) set. Expression of 11 target genes was measured by quantitative PCR in resected tumors. A risk score to predict overall survival (OS) was generated and validated. Intra-tumoral heterogeneity was assessed by analyzing 50 tumor areas from 10 patients. - Results - A risk score including the expression of CCL5, CTNNB1, EXOSC3 and LZTR1 and the clinical parameters cT, tumor localization and histopathologic type suggested two groups with a significant difference in OS [hazard ratio (HR) 0.30; 95% confidence interval (CI) 0.17-0.52]. The risk score was successfully validated in an independent cohort (HR 0.32; 95% CI 0.21-0.51; P < 0.001) as well as in subgroups of primarily resected (HR 0.30; 95% CI 0.17-0.54; P < 0.001) and pre-/perioperatively treated patients (HR 0.37; 95% CI 0.17-0.81; P = 0.009). A significant difference in OS of high- and low-risk patients was also found in primarily resected patients with intestinal (HR 0.45; 95% CI 0.23-0.90; P = 0.020) and nonintestinal-type carcinomas (HR 0.1; 95% CI 0.02-0.42; P < 0.001). Intra-tumor heterogeneity analysis indicated a classification reliability of 95% for a supposed analysis of three biopsies. - Conclusion - The identified risk score could substantially contribute to an improved management of gastric cancer patients in the context of perioperative chemotherapy. 
650 4 |a gastric carcinoma 
650 4 |a gene expression 
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