Minami Seigo, Ogata Yoshitaka, Ihara Shouichi, Yamamoto Suguru, Komuta Kiyoshi
Department of Respiratory Medicine, Osaka Police Hospital, Osaka, Japan.
Lung Cancer (Auckl). 2017 Dec 8;8:249-257. doi: 10.2147/LCTT.S142880. eCollection 2017.
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.
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.
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, <0.01) and higher PNI (HR 0.50, 95% CI 0.31-0.78, <0.01) as prognostic factors for longer OS. However, neither biomarker was predictive of PFS.
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.
多种生物标志物已被证明可预测各类癌症的预后。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)基于血清白蛋白水平和C反应蛋白(CRP)。预后营养指数(PNI)是血清白蛋白水平与绝对淋巴细胞计数的组合。本研究旨在评估mGPS和PNI在SCLC中的预后价值。
我们回顾性分析并计算了2007年11月至2016年6月期间开始接受铂类联合化疗的IIIB期或IV期SCLC患者的mGPS和PNI。我们比较了这两种生物标志物高低分组之间的总生存期(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。
我们回顾了97例SCLC患者。mGPS为0 - 1且PNI较高的患者的OS明显长于mGPS为2且PNI较低的患者。mGPS为0 - 1的患者的PFS明显长于mGPS为2的患者,而根据PNI的PFS无显著差异。多因素分析发现mGPS为0 - 1(风险比[HR] 2.34,95%置信区间[CI] 1.27 - 4.31,<0.01)和较高的PNI(HR 0.50,95% CI 0.31 - 0.78,<0.01)是OS更长的预后因素。然而,这两种生物标志物均不能预测PFS。
我们的研究是一项小型回顾性研究;然而,数据表明治疗前的mGPS和PNI是晚期SCLC患者OS的独立预测指标。治疗前对mGPS和PNI的评估可能有助于识别预后不良的患者。我们建议治疗前测量血清白蛋白、C反应蛋白和绝对淋巴细胞计数。