Zhang Peng, Xi Mian, Li Qiao-Qiao, He Li-Ru, Liu Shi-Liang, Zhao Lei, Shen Jing-Xian, Liu Meng-Zhong
1. Sun Yat-sen University Cancer Center; State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine; Department of Radiation Oncology, Cancer Center, Sun Yat-sen University, Guangzhou 510060, People's Republic of China.
2. Sun Yat-sen University Cancer Center; State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine; Imaging Diagnosis and Interventional Center, Cancer Center, Sun Yat-sen University, Guangzhou 510060, People's Republic of China.
J Cancer. 2014 Sep 6;5(8):689-95. doi: 10.7150/jca.9569. eCollection 2014.
There is increasing evidence that the presence of an inflammation-based prognostic score (modified Glasgow prognostic score, mGPS) is associated with survival in patients with advanced cancer. This study aimed to assess whether the mGPS has prognostic value in patients with thoracic esophageal squamous cell carcinoma undergoing chemoradiotherapy.
A total of 212 patients undergoing chemoradiotherapy for newly-diagnosed esophageal squamous cell carcinoma between October, 2006 and December, 2011 were retrospectively analyzed. Serum C-reactive protein (CRP) and albumin were measured before initiation of treatment. The relationships between the mGPS and other relevant variables including white blood cell count, neutrophilic granulocyte count, platelet count, hemoglobin, bilirubin, aspartate aminotransferase (AST), alanine aminotransferase (ALT) and lactate dehydrogenase (LDH) were analyzed. Overall survival (OS) and progression-free survival (PFS) were calculated. Significant prognostic factors were identified using univariate and multivariate analyses.
Three-year OS for all patients was 24.6%; 3-year PFS was 21.3%. Patients with a mGPS of 0, 1 and 2 were 90, 78, 44, respectively. Higher mGPS was related to higher white blood cell, neutrophilic granulocyte and platelet counts, and lower total bilirubin. T stage, M stage and mGPS were independent prognostic indicators for OS; T stage, M stage, mGPS and platelet count were independent prognostic indicators for PFS.
Pretreatment mGPS is an easily measurable significant prognostic factor and can be used in combination with conventional TNM staging to predict survival in patients with squamous cell carcinoma undergoing chemoradiotherapy.
越来越多的证据表明,基于炎症的预后评分(改良格拉斯哥预后评分,mGPS)与晚期癌症患者的生存率相关。本研究旨在评估mGPS在接受放化疗的胸段食管鳞状细胞癌患者中是否具有预后价值。
回顾性分析2006年10月至2011年12月期间212例新诊断的食管鳞状细胞癌接受放化疗的患者。在开始治疗前检测血清C反应蛋白(CRP)和白蛋白。分析mGPS与其他相关变量之间的关系,包括白细胞计数、中性粒细胞计数、血小板计数、血红蛋白、胆红素、天冬氨酸转氨酶(AST)、丙氨酸转氨酶(ALT)和乳酸脱氢酶(LDH)。计算总生存期(OS)和无进展生存期(PFS)。采用单因素和多因素分析确定显著的预后因素。
所有患者的3年总生存率为24.6%;3年无进展生存率为21.3%。mGPS为0、1和2的患者分别为90、78和44例。较高的mGPS与较高的白细胞、中性粒细胞和血小板计数以及较低的总胆红素相关。T分期、M分期和mGPS是总生存期的独立预后指标;T分期、M分期、mGPS和血小板计数是无进展生存期的独立预后指标。
治疗前mGPS是一个易于测量的显著预后因素,可与传统的TNM分期联合使用,以预测接受放化疗的鳞状细胞癌患者的生存率。