A. Gerger, Austrian Breast, E. Bareck, G. V. Pelt, H. Rabl, H. Gelderblom, K. Geissler, M. Filipits, M. Gnant, P. Götzinger, R. Schaberl-Moser, R. Greil, R. Tollenaar, Stefan W. de Vroome, S. Zunder, T. Bachleitner-Hofmann, W. Mesker, W. Hilbe
{"title":"Prognostic and Predictive Value of the Tumor-Stroma Ratio in STAGE II Colon Cancer","authors":"A. Gerger, Austrian Breast, E. Bareck, G. V. Pelt, H. Rabl, H. Gelderblom, K. Geissler, M. Filipits, M. Gnant, P. Götzinger, R. Schaberl-Moser, R. Greil, R. Tollenaar, Stefan W. de Vroome, S. Zunder, T. Bachleitner-Hofmann, W. Mesker, W. Hilbe","doi":"10.31487/j.cor.2020.04.12","DOIUrl":null,"url":null,"abstract":"Background: Tumor-stroma ratio (TSR) is an independent prognosticator in colon cancer.\nObjective: We set out to investigate the predictive power, as well as to validate the prognostic power of\nTSR in stage II colon cancer patients. Better identification of patients who could benefit from adjuvant\nchemotherapy remains an important issue in stage II disease.\nMethods: TSR was microscopically determined on haematoxylin and eosin-stained primary tumor tissue\nslides of 212 patients who received either adjuvant chemotherapy or surveillance after curative resection in\na prospective randomized clinical trial (ABCSG-91).\nResults: Stroma-high tumors were associated with significantly more cancer-related death ((CaDeath) HR\n2.30, 95% CI 1.05−5.03; p=0.037) and significantly shorter distant recurrence-free survival ((DRFS) HR\n2.32, 95% CI 1.10−4.87; p=0.027) compared to stroma-low tumors. Backward multivariate Cox-regression\nanalysis demonstrated TSR as an independent prognosticator for DRFS (p=0.027) and CaDeath (p=0.031).\nTSR did not validate as a predictive biomarker; CaDeath (HR 0.87, 95% CI 0.18−4.17; p=0.87), DRFS (HR\n0.76, 95% CI 0.17−3.36; p=0.71) and OS (HR 0.96, 95% CI 0.29−3.21; p=0.95) for the type of\nchemotherapy given in ABCSG-91.\nConclusions: TSR, an easily applicable and inexpensive observer-based method, is an independent\npredictor of poor prognosis in stage II colon cancer. Predictive value for adjuvant 5-FU/leucovorin could\nnot be demonstrated.","PeriodicalId":10487,"journal":{"name":"Clinical Oncology and Research","volume":"40 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2020-04-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Clinical Oncology and Research","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.31487/j.cor.2020.04.12","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1
Abstract
Background: Tumor-stroma ratio (TSR) is an independent prognosticator in colon cancer.
Objective: We set out to investigate the predictive power, as well as to validate the prognostic power of
TSR in stage II colon cancer patients. Better identification of patients who could benefit from adjuvant
chemotherapy remains an important issue in stage II disease.
Methods: TSR was microscopically determined on haematoxylin and eosin-stained primary tumor tissue
slides of 212 patients who received either adjuvant chemotherapy or surveillance after curative resection in
a prospective randomized clinical trial (ABCSG-91).
Results: Stroma-high tumors were associated with significantly more cancer-related death ((CaDeath) HR
2.30, 95% CI 1.05−5.03; p=0.037) and significantly shorter distant recurrence-free survival ((DRFS) HR
2.32, 95% CI 1.10−4.87; p=0.027) compared to stroma-low tumors. Backward multivariate Cox-regression
analysis demonstrated TSR as an independent prognosticator for DRFS (p=0.027) and CaDeath (p=0.031).
TSR did not validate as a predictive biomarker; CaDeath (HR 0.87, 95% CI 0.18−4.17; p=0.87), DRFS (HR
0.76, 95% CI 0.17−3.36; p=0.71) and OS (HR 0.96, 95% CI 0.29−3.21; p=0.95) for the type of
chemotherapy given in ABCSG-91.
Conclusions: TSR, an easily applicable and inexpensive observer-based method, is an independent
predictor of poor prognosis in stage II colon cancer. Predictive value for adjuvant 5-FU/leucovorin could
not be demonstrated.