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

被引:15
作者
Bauer, L. [1 ]
Hapfelmeier, A. [2 ]
Blank, S. [3 ]
Reiche, M. [1 ]
Slotta-Huspenina, J. [1 ]
Jesinghaus, M. [1 ]
Novotny, A. [4 ]
Schmidt, T. [3 ]
Grosser, B. [1 ]
Kohlruss, M. [1 ]
Weichert, W. [1 ,5 ]
Ott, K. [6 ]
Keller, G. [1 ]
机构
[1] Tech Univ Munich, Dept Pathol, Trogerstr 18, D-81675 Munich, Germany
[2] Tech Univ Munich, Dept Med Stat & Epidemiol, Munich, Germany
[3] Heidelberg Univ, Dept Surg, Heidelberg, Germany
[4] Tech Univ Munich, Dept Surg, Munich, Germany
[5] Tech Univ Munich, Partner Site Munich, German Canc Consortium DKTK, Dept Pathol, Munich, Germany
[6] Klinikum Rosenheim, Dept Surg, Rosenheim, Germany
关键词
gastric carcinoma; prognosis; risk score; perioperative chemotherapy; gene expression; PERIOPERATIVE CHEMOTHERAPY; ADENOCARCINOMA; DIAGNOSIS; SURVIVAL; JUNCTION; SUBTYPES; SURGERY;
D O I
10.1093/annonc/mdx685
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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.
引用
收藏
页码:127 / 132
页数:6
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