Tumor microenvironment characteristics association with clinical outcome in patients with resected intestinal-type gastric cancer

Author:

Tian Chun-Fang1ORCID,Jing Hai-Yan2,Sinicrope Frank A3,Wang Jin-Shen4,Gao Bin-Bin1,Sun Xiao-Gang1,Yao Zhi-Gang2ORCID,Li Le-Ping4,Saberzadeh-Ardestani Bahar5,Song Wei1,Sha Dan1ORCID

Affiliation:

1. Shandong Provincial Hospital Affiliated to Shandong First Medical University Department of Minimally Invasive Treatment of Cancer, , Jinan, 250021, Shandong , People’s Republic of China

2. Shandong Provincial Hospital Affiliated to Shandong First Medical University Department of Pathology, , Jinan, 250021, Shandong , People’s Republic of China

3. Mayo Clinic Department of Oncology, , Rochester, 55905 ,  United States

4. Shandong Provincial Hospital Affiliated to Shandong First Medical University Department of Gastrointestinal Surgery, , Jinan, 250021, Shandong , People’s Republic of China

5. Mayo Clinic Gastrointestinal Research Unit, , Rochester, 55905 ,  United States

Abstract

Abstract Background Tumor microenvironment (TME) characteristics including tumor stroma ratio (TSR), tumor budding (TB), and tumor-infiltrating lymphocytes (TILs) were examined in resected gastric cancer. These TME features have been shown to indicate metastatic potential in colon cancer, and intestinal-type gastric cancer (IGC) has pathological similarities with that malignancy. Methods TSR, TB, and TILs were quantified in routine histological sections from 493 patients with IGC who underwent radical resection at 2 university hospitals in China from 2010 to 2016. TME variables were dichotomized as follows: TSR (50%), TILs (median), TB per international guidelines (4 buds/0.785mm2), and platelet-lymphocyte ratio (PLR) per survival ROC. Association of TME features with patient clinicopathological characteristics, time-to-recurrence (TTR), and cancer-specific-survival (CSS) were examined using univariate and multivariate analysis, including a relative contribution analysis by Cox regression. Results Patients whose tumors showed high TSR or high TB or low TILs were each significantly associated with increased T and N stage, higher histological grade, and poorer TTR and CSS at 5 years. Only TSR and N stage were independently associated with TTR and CSS after adjustment for covariates. PLR was only independently associated with TTR after adjustment for covariates. Among the variables examined, only TSR was significantly associated with both TTR (HR 1.72, 95% CI, 1.14-2.60, P = .01) and CSS (HR 1.62, 95% CI, 1.05-2.51, P = .03) multivariately. Relative contribution to TTR revealed that the top 3 contributors were N stage (45.1%), TSR (22.5%), and PLR (12.9%), while the top 3 contributors to CSS were N stage (59.9%), TSR (14.7%), and PLR (10.9%). Conclusions Among the examined TME features, TSR was the most robust for prognostication and was significantly associated with both TTR and CSS. Furthermore, the relative contribution of TSR to patient TTR and CSS was second only to nodal status.

Publisher

Oxford University Press (OUP)

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