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Glasgow prognostic score is an independent marker for poor prognosis with all cases of epithelial ovarian cancer

机译:格拉斯哥预后评分是所有上皮性卵巢癌预后不良的独立指标

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摘要

Inflammatory markers are important prognostic factors in various cancers. This study investigated whether inflammatory markers of the Glasgow prognostic score (GPS) predicted progression‐free survival (PFS) and overall survival (OS) for patients with all cases of epithelial ovarian cancer (OC). Pretreatment GPS was examined for the correlations with PFS and OS in 216 patients in all stages of epithelial OC. Statistical analyses were performed using the Mann–Whitney U‐test. PFS and OS were analyzed using the Kaplan–Meier method. Cox's proportional hazard regression was used for univariate and multivariate analyses. For all patients, the median PFS was 35.1 months, and median OS was 46.7 months; follow‐up range was 1–162 months. Kaplan–Meier analysis revealed that patients with high GPS (GPS 2) at pretreatment had a shorter PFS and OS than did patients with lower style="fixed-case">GPS ( style="fixed-case">GPS 0 + 1) in for early, advanced, and all‐stages of style="fixed-case">OC ( style="fixed-case">PFS: P < 0.001 for early‐, advanced‐ and all‐stages; style="fixed-case">OS; P < 0.001 for early‐ and all‐stage, P = 0.015 for advanced‐stage). style="fixed-case">GPS ( style="fixed-case">GPS 2) was also found to be an independent predictor of both recurrence (P = 0.002) and survival (P = 0.001) of all cases of epithelial style="fixed-case">OC by a multivariate analysis. style="fixed-case">GPS can serve as an indicator of poor prognosis in patients with all stages of epithelial style="fixed-case">OC, including early‐stage disease and regardless of histology.
机译:炎症标志物是各种癌症的重要预后因素。这项研究调查了格拉斯哥预后评分(GPS)的炎症指标是否可预测所有上皮性卵巢癌(OC)患者的无进展生存期(PFS)和总体生存期(OS)。在216例上皮OC的患者中,检查了治疗前GPS与PFS和OS的相关性。使用Mann-Whitney U检验进行统计分析。使用Kaplan-Meier方法分析了PFS和OS。 Cox的比例风险回归用于单变量和多变量分析。对于所有患者,中位PFS为35.1个月,中位OS​​为46.7个月;随访范围为1–162个月。 Kaplan–Meier分析显示,相比于 style =“ fixed-case”> GPS ( style =“ fixed- case“> GPS 0 + 1,用于 style =” fixed-case“> OC ( style =” fixed-case“> PFS的早期,高级和所有阶段:对于早期,高级和所有阶段,P <0.001;对于早期和所有阶段, style =“ fixed-case”> OS ;对于早期和所有阶段,P <0.001,对于P和P = 0.015高级)。还发现 style =“ fixed-case”> GPS ( style =“ fixed-case”> GPS 2)是复发的独立预测因子(P = 0.002)和通过多变量分析得出所有上皮 style =“ fixed-case”> OC 病例的生存率(P = 0.001)。 style =“ fixed-case”> GPS 可以作为上皮 style =“ fixed-case”> OC 所有阶段(包括早期)的患者预后不良的指标疾病,无论组织学如何。

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