Department of Urology, Huangshi Central Hospital (Pu Ai Hospital), Affiliated Hospital of Hubei Polytechnic University, Edong Healthcare Group, Huangshi, Hubei,China.
Department of Abdominal and Pelvic Medical Oncology II ward, Huangshi Central Hospital (Pu Ai Hospital), Affiliated Hospital of Hubei Polytechnic University, Edong Healthcare Group, Huangshi, Hubei, China.
PLoS One. 2019 Oct 23;14(10):e0224266. doi: 10.1371/journal.pone.0224266. eCollection 2019.
Growing evidence has revealed that pretreatment C-reactive protein to albumin ratio (CAR) are associated with prognosis for patients with renal cell carcinoma (RCC). However, inconsistent findings have been reported, which promote us to summarize the global predicting role of CAR for survival in RCC patients.
Two reviewers independently retrieved the literature on EMBASE, MEDLINE, and Cochrane Library databases for eligible studies evaluating the associations of CAR with survival. Data related to the overall survival (OS), disease-free survival (DFS), progress-free survival (PFS), and clinicopathological features were extracted and pooled using meta-analysis with fixed or random- effect models when applicable.
Eight studies including 2,829 patients were analyzed in the present study. High pretreatment CAR was associated with worse OS (pooled HR: 2.14, 95% CI = 1.64-2.79, p < 0.001) and DFS/PFS (pooled HR: 1.75, 95% CI: 1.31-2.35, P < 0.001). Moreover, high CAR was correlated with performance status (≥ 1), tumor location (left), Fuhrman grade (3-4), TNM stage (III-IV), T stage (T3-4), N stage (N1), M stage (M1), tumor necrosis (yes), venous thrombus (positive), metastasis at diagnosis (yes), NLR (> median), and PLR (> median).
High pretreatment CAR is effectively predictive of worse survival in patients with RCC and could be a prognostic biomarker for those patients.
越来越多的证据表明,治疗前 C 反应蛋白与白蛋白比值(CAR)与肾细胞癌(RCC)患者的预后相关。然而,已有研究结果并不一致,这促使我们对 CAR 预测 RCC 患者生存的全球作用进行总结。
两位审查员分别从 EMBASE、MEDLINE 和 Cochrane 图书馆数据库中检索评估 CAR 与生存相关性的合格研究文献。使用固定或随机效应模型进行荟萃分析,提取并汇总与总生存期(OS)、无病生存期(DFS)、无进展生存期(PFS)和临床病理特征相关的数据。
本研究共分析了 8 项研究,包括 2829 例患者。高预处理 CAR 与较差的 OS(合并 HR:2.14,95%CI=1.64-2.79,p<0.001)和 DFS/PFS(合并 HR:1.75,95%CI:1.31-2.35,P<0.001)相关。此外,CAR 升高与表现状态(≥1)、肿瘤位置(左侧)、Fuhrman 分级(3-4)、TNM 分期(III-IV)、T 分期(T3-4)、N 分期(N1)、M 分期(M1)、肿瘤坏死(是)、静脉血栓(阳性)、诊断时转移(是)、中性粒细胞与淋巴细胞比值(NLR)(>中位数)和血小板与淋巴细胞比值(PLR)(>中位数)相关。
高预处理 CAR 可有效预测 RCC 患者的生存情况较差,可能是这些患者的预后生物标志物。