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Predictive value of the modified Glasgow Prognostic Score for the therapeutic effects of molecular-targeted drugs on advanced renal cell carcinoma

机译:改良的格拉斯哥预后评分对分子靶向药物治疗晚期肾细胞癌的预测价值

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摘要

Inflammation is considered to be a prognostic factor for renal cell carcinoma (RCC). An inflammation-based prognostic score (modified Glasgow Prognostic Score; mGPS) is widely used for preoperative patients; however, little information is available regarding its prognostic value in patients with RCC treated with molecular-targeted drugs. A total of 32 advanced and recurrent RCC patients initially treated with molecular-targeted drugs from October, 2009 to August, 2015 were retrospectively investigated. Information on patient characteristics prior to treatment initiation and the clinical course were retrieved from clinical records. The correlation between survival and patient variables was analyzed. Survival was compared among patient groups according to the mGPS score. The median patient age was 66 years. The percentage of patients with an Eastern Cooperative Oncology Group performance status of 0 or 1 was 87.5, and 65.6% of the RCCs were clear cell carcinomas. A Memorial Sloan-Kettering Cancer Center index of good or intermediate was determined for 75% of the patients. Sunitinib, pazopanib or sorafenib was administered to 56, 22 and 13% of the cases, respectively. An mGPS score of 0, 1 and 2 was calculated for 66, 9 and 25% of the cases, respectively. Patients in the mGPS low group (score 0) exhibited significantly better progression-free survival (PFS) and overall survival (OS) compared with patients in the mGPS high group (score 1 or 2) (median PFS, 307 vs. 70 days and median OS, 1,081 vs. 140 days, respectively). In conclusion, inflammatory status as assessed by the mGPS score was closely associated with the prognosis of RCC patients treated with molecular-targeted therapy.
机译:炎症被认为是肾细胞癌(RCC)的预后因素。基于炎症的预后评分(改良的格拉斯哥预后评分; mGPS)被广泛用于术前患者。然而,有关其在以分子靶向药物治疗的RCC患者中的预后价值的信息很少。回顾性调查了2009年10月至2015年8月最初接受分子靶向药物治疗的32例晚期和复发性RCC患者。从临床记录中检索治疗开始和临床过程之前的患者特征信息。分析了生存与患者变量之间的相关性。根据mGPS评分比较患者组的生存率。患者的中位年龄为66岁。东部合作肿瘤小组表现状态为0或1的患者百分比为87.5,并且65.6%的RCC是透明细胞癌。确定了75%的患者的Sloan-Kettering纪念中心的良好或中等指数。舒尼替尼,帕唑帕尼或索拉非尼分别用于56%,22%和13%的病例。分别针对66%,9%和25%的案例计算了mGPS得分0、1和2。与mGPS高组(评分1或2)相比,mGPS低组(评分0)的患者表现出更好的无进展生存期(PFS)和总生存期(OS)(中位PFS:307天vs 70天,中位数操作系统分别为1,081和140天)。总之,通过mGPS评分评估的炎症状态与接受分子靶向治疗的RCC患者的预后密切相关。

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