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Assessment of prognostic factors after primary tumor resection in metastatic colon cancer patients: A Veteran's Affairs Central Cancer Registry (VACCR) analysis, 1995-2008

机译:转移性结肠癌患者原发肿瘤切除后的预后因素评估:退伍军人事务中心癌症登记处(VACCR)分析,1995-2008年

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Background Resection of the primary tumor in metastatic colon cancer may occur for palliation of bleeding or obstruction despite distant metastases. This study evaluates clinicopathologic features that serve as prognostic markers in those patients with stage IV colon cancer who undergo resection of their primary tumor. Methods Retrospective analysis of stage IV colon cancer patients who underwent surgical resection of the primary tumor from 1995 to 2008 was done via the Veteran's Affairs Central Cancer Registry. Age, Charlson co-morbidity index score, extent of metastases, sex, number of lymph nodes examined, lymph node ratio (LNR), type of surgery, use of adjuvant chemotherapy, primary tumor site, and grade were studied with respect to overall survival by using log-rank and Kaplan-Meier analysis. Results There were 2,625 patients with stage IV colon cancer who had primary tumor resection. Age at diagnosis, Charlson co-morbidity index score, lymph node ratio, and use of chemotherapy were found to be independent predictors of survival by multivariate analysis. Conclusion Clinicopathologic factors such as LNR, use of chemotherapy, age, co-morbidities, site of primary colon tumor, and number of sites of metastasis are all independent predictors of overall survival in patients who undergo primary colon tumor resection in the metastatic setting. J. Surg. Oncol. 2012; 106:486-490.
机译:背景转移性结肠癌的原发肿瘤切除可能是为了减轻出血或阻塞,尽管有远处转移。这项研究评估了那些接受原发性肿瘤切除的IV期结肠癌患者的临床病理特征,作为预后标志物。方法通过Veteran's Affairs中央癌症登记处对1995年至2008年接受原发肿瘤手术切除的IV期结肠癌患者进行回顾性分析。年龄,Charlson合并症指数评分,转移程度,性别,检查的淋巴结数目,淋巴结比率(LNR),手术类型,辅助化疗的使用,原发肿瘤部位和等级均针对总生存期进行了研究通过使用对数秩和Kaplan-Meier分析。结果共有2625例IV期结肠癌患者接受了原发性肿瘤切除。通过多变量分析发现,诊断时的年龄,Charlson合并症指数评分,淋巴结比率和化疗的使用是生存的独立预测因素。结论LNR,化疗的使用,年龄,合并症,原发性结肠肿瘤的部位和转移部位的数量等临床病理因素都是转移性原发性结肠癌切除患者总体生存的独立预测因素。 J. Surg。 Oncol。 2012; 106:486-490。

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