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":"肿瘤-间质比对II期结肠癌的预后和预测价值","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":"{\"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}","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
摘要
背景:肿瘤间质比(TSR)是结肠癌的独立预后指标。目的:探讨tsr在II期结肠癌患者中的预测能力,并验证其预后能力。在II期疾病中,更好地识别可以从辅助化疗中获益的患者仍然是一个重要问题。方法:在前瞻性随机临床试验(ABCSG-91)中,对212例接受辅助化疗或治疗性切除后接受监测的患者的原发肿瘤组织切片,在显微镜下测定血色素和伊红染色的TSR。结果:间质高的肿瘤与更多的癌症相关死亡相关((CaDeath) HR2.30, 95% CI 1.05−5.03;p=0.037),远端无复发生存期显著缩短((DRFS) HR2.32, 95% CI 1.10−4.87;P =0.027)。多变量反向cox回归分析显示TSR是DRFS (p=0.027)和CaDeath (p=0.031)的独立预测因子。TSR未被证实为预测性生物标志物;CaDeath (HR 0.87, 95% CI 0.18−4.17;p=0.87), DRFS (HR0.76, 95% CI 0.17−3.36;p=0.71)和OS (HR 0.96, 95% CI 0.29−3.21;p=0.95)与ABCSG-91的化疗类型有关。结论:TSR是一种易于应用且价格低廉的基于观察者的方法,是II期结肠癌预后不良的独立预测指标。辅助5-FU/亚叶酸素的预测价值无法证明。
Prognostic and Predictive Value of the Tumor-Stroma Ratio in STAGE II Colon Cancer
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.