预处理格拉斯哥预后评分和预后营养指数预测晚期小细胞肺癌患者的总生存期。

IF 5.1 Q1 ONCOLOGY
Lung Cancer: Targets and Therapy Pub Date : 2017-12-08 eCollection Date: 2017-01-01 DOI:10.2147/LCTT.S142880
Seigo Minami, Yoshitaka Ogata, Shouichi Ihara, Suguru Yamamoto, Kiyoshi Komuta
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引用次数: 36

摘要

背景:各种生物标志物已被证明可以预测各种类型癌症的预后。然而,这些生物标志物尚未在晚期小细胞肺癌(SCLC)中进行研究。改良格拉斯哥预后评分(mGPS)是基于血清白蛋白水平和c反应蛋白(CRP)。预后营养指数(PNI)是血清白蛋白水平和绝对淋巴细胞计数的组合。本研究旨在评价mGPS和PNI在SCLC中的预后价值。方法:我们回顾性回顾并计算了2007年11月至2016年6月期间开始以铂为基础的联合化疗的IIIB或IV期SCLC患者的mGPS和PNI。我们比较了这两种生物标志物高组和低组的总生存期(OS)和无进展生存期(PFS)。单因素和多因素Cox风险分析评估了这些生物标志物的预后价值。结果:我们回顾了97例SCLC患者。mGPS 0-1和高PNI患者的OS明显长于mGPS 2和低PNI患者。mGPS 0-1组的PFS明显长于mGPS 2组,但PNI差异无统计学意义。多因素分析发现mGPS 0-1(风险比[HR] 2.34, 95%可信区间[CI] 1.27-4.31, ppp)。然而,数据表明预处理mGPS和PNI是晚期SCLC患者OS的独立预测因子。mGPS和PNI的预处理评估可能有助于鉴别预后不良的患者。我们建议预处理血清白蛋白、c反应蛋白和绝对淋巴细胞计数。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Pretreatment Glasgow prognostic score and prognostic nutritional index predict overall survival of patients with advanced small cell lung cancer.

Pretreatment Glasgow prognostic score and prognostic nutritional index predict overall survival of patients with advanced small cell lung cancer.

Pretreatment Glasgow prognostic score and prognostic nutritional index predict overall survival of patients with advanced small cell lung cancer.

Background: Various biomarkers have been shown to predict prognosis in various types of cancers. However, these biomarkers have not been studied in advanced small cell lung cancer (SCLC). The modified Glasgow prognostic score (mGPS) is based on serum albumin level and C-reactive protein (CRP). The prognostic nutritional index (PNI) is a combination of serum albumin level and absolute lymphocyte count. This study aimed to evaluate the prognostic value of mGPS and PNI in SCLC.

Methods: We retrospectively reviewed and calculated mGPS and PNI for patients with stage IIIB or IV SCLC who initiated platinum-based combination chemotherapy between November 2007 and June 2016. We compared overall survival (OS) and progression-free survival (PFS) between high and low groups of these two biomarkers. Univariate and multivariate Cox hazard analyses assessed the prognostic value of these biomarkers.

Results: We reviewed 97 SCLC patients. The OS of patients with mGPS 0-1 and higher PNI was significantly longer than that of those with mGPS 2 and lower PNI. The PFS of mGPS 0-1 was significantly longer than that of mGPS 2, while there was no significant difference in PFS according to PNI. Multivariate analyses found mGPS 0-1 (hazard ratio [HR] 2.34, 95% confidence interval [CI] 1.27-4.31, P<0.01) and higher PNI (HR 0.50, 95% CI 0.31-0.78, P<0.01) as prognostic factors for longer OS. However, neither biomarker was predictive of PFS.

Conclusion: Our study was a small retrospective study; however, the data demonstrate that pretreatment mGPS and PNI are independent predictors of OS in patients with advanced SCLC. The pretreatment assessment of mGPS and PNI may be useful for identification of patients with poor prognosis. We recommend pretreatment measurement of serum albumin, C-reactive protein, and absolute lymphocyte count.

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CiteScore
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