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Performance of risk stratification systems for gastrointestinal stromal tumors: A multicenter study 被引量:2
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作者 Tao Chen Liang-Ying Ye +11 位作者 Xing-Yu Feng Hai-Bo Qiu Peng Zhang Yi-Xin Luo Li-Yi Yuan Xin-Hua Chen Yan-Feng Hu Hao Liu Yong Li Kai-Xiong Tao Jiang Yu Guo-Xin Li 《World Journal of Gastroenterology》 SCIE CAS 2019年第10期1238-1247,共10页
BACKGROUND Gastrointestinal stromal tumors(GISTs) are the most common mesenchymal tumor type in the gastrointestinal system. Presently, various classification systems to prognosticate GISTs have been proposed.AIM To e... BACKGROUND Gastrointestinal stromal tumors(GISTs) are the most common mesenchymal tumor type in the gastrointestinal system. Presently, various classification systems to prognosticate GISTs have been proposed.AIM To evaluate the application value of four different risk stratification systems for GISTs.METHODS Patients who were diagnosed with GISTs and underwent surgical resection at four hospitals from 1998 to 2015 were identified from a database. Risk of recurrence was stratified by the modified National Institute of Health(NIH)criteria, the Armed Forces Institute of Pathology(AFIP) criteria, the Memorial Sloan Kettering Cancer Center(MSKCC) prognostic nomogram, and the contour maps. Receiver operating characteristic(ROC) curves were established to compare the four abovementioned risk stratification systems based on the area under the curve(AUC).RESULTS A total of 1303 patients were included in the study. The mean age of the patients was 55.77 ± 13.70 yr; 52.3% of the patients were male. The mean follow-up period was 64.91 ± 35.79 mo. Approximately 67.0% the tumors were located in the stomach, and 59.5% were smaller than 5 cm; 67.3% of the patients had a mitotic count ≤ 5/50 high-power fields(HPFs). Thirty-four tumors ruptured before and during surgery. Univariate analysis demonstrated that tumor size > 5 cm(P <0.05), mitotic count > 5/50 HPFs(P < 0.05), non-gastric location(P < 0.05), and tumor rupture(P < 0.05) were significantly associated with increased recurrence rates. According to the ROC curve, the AFIP criteria showed the largest AUC(0.754).CONCLUSION According to our data, the AFIP criteria were associated with a larger AUC than the NIH modified criteria, the MSKCC nomogram, and the contour maps, which might indicate that the AFIP criteria have better accuracy to support therapeutic decision-making for patients with GISTs. 展开更多
关键词 GASTROINTESTINAL STROMAL TUMORS risk STRATIFICATION Prognosis Modified National Institute of Health CRITERIA Armed Forces Institute of Pathology CRITERIA memorial Sloan Kettering cancer center prognostic nomogram Contour maps GASTROINTESTINAL TUMORS
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MSKCC生存危险度分组在中国肾癌靶向治疗人群中的验证 被引量:7
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作者 洪雅萍 朱耀 +10 位作者 姚旭东 张世林 戴波 张海梁 沈益君 朱一平 马春光 肖文军 秦晓健 林国文 叶定伟 《中华泌尿外科杂志》 CAS CSCD 北大核心 2013年第2期143-146,共4页
目的探讨分子靶向治疗晚期肾癌患者的疗效并对MSKCC危险度分组预后模型进行验证。方法晚期肾癌患者345例,年龄17~90岁,平均57岁。其中透明细胞癌306例,乳头状。肾癌20例,嫌色细胞癌4例,肾集合管癌5例,髓样癌3例,未分类癌7例。... 目的探讨分子靶向治疗晚期肾癌患者的疗效并对MSKCC危险度分组预后模型进行验证。方法晚期肾癌患者345例,年龄17~90岁,平均57岁。其中透明细胞癌306例,乳头状。肾癌20例,嫌色细胞癌4例,肾集合管癌5例,髓样癌3例,未分类癌7例。常见转移部位为肺、骨和淋巴结。治疗方法:索拉非尼组205例,索拉非尼口服,400mg,2次/d连续服药;舒尼替尼组140例,舒尼替尼口服,50mg每天,用药4周,间歇2周为一个疗程。采用Kaplan—Meier法对生存资料进行分析,采用Log—rank检验和一致系数分析法对MSKCC危险度分组模型进行验证。结果总体中位随访时间23个月,中位总生存时间33个月,1、2、3年生存率分别为77.6%、59.3%、46.6%。根据MSKCC危险度分组,低、中、高危组分别169、150、26例,中位总生存时间分别为46、24、8个月(P〈0.01),2年生存率分别为75.8%、47.7%、10.1%。MSKCC危险度分组预测模型的一致系数为0.687。结论分子靶向治疗在我国晚期。肾癌人群具有良好的临床疗效,MSKCC模型验证不仅有利于个体化的肿瘤预后判断,而且有利于与患者的交流和临床用药选择。 展开更多
关键词 肾细胞 分子靶向治疗 预后 MSKCC危险度分组
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