Department of Radiation Oncology, Winship Cancer Institute, Emory University, Atlanta, Georgia.
Cancer. 2013 Sep 1;119(17):3148-55. doi: 10.1002/cncr.28144. Epub 2013 May 29.
Mixed lineage kinase domain-like protein (MLKL) is a necrosome component mediating programmed necrosis that may be an important determinant of cancer cell death. The goal of the current study was to evaluate the prognostic value of MLKL expression in patients with pancreatic adenocarcinoma (PAC).
Tissue from 80 patients was collected from a prospectively maintained database of patients with PAC who underwent pancreaticoduodenectomy between January 2000 and October 2008. Immunohistochemistry analysis was performed and scored using an established scoring system. Kaplan-Meier survival curves were generated for recurrence-free survival (RFS) and overall survival (OS) for all patients and for patients receiving adjuvant chemotherapy. MLKL scores were correlated with RFS and OS using univariate and multivariate Cox regression analyses incorporating clinically relevant covariates.
The median age of the patients was 63 years and 53% were men. Low MLKL expression was associated with decreased OS (6 months vs 17 months; P = .006). In the subset of 59 patients who received adjuvant chemotherapy, low MLKL expression was associated with decreased RFS (5 months vs 15 months; P = .006) and decreased OS (6 months vs 19 months; P < .0001). On multivariate analysis, low MLKL expression was associated with poor OS in all patients (hazards ratio, 4.6 [95% confidence interval, 1.6-13.8]; P = .006) and in patients receiving adjuvant chemotherapy (hazards ratio, 8.1 [95% confidence interval, 2.2-29.2]; P = .002).
Low expression of MLKL is associated with decreased OS in patients with resected PAC and decreased RFS and OS in the subset of patients with resected PAC who receive adjuvant chemotherapy. The use of this biomarker in patients with PAC may provide important prognostic information.
混合谱系激酶结构域样蛋白(MLKL)是一种坏死小体组成部分,介导程序性坏死,可能是癌细胞死亡的重要决定因素。本研究的目的是评估 MLKL 在胰腺导管腺癌(PAC)患者中的表达对预后的影响。
从 2000 年 1 月至 2008 年 10 月间接受胰十二指肠切除术的 PAC 患者前瞻性维护的数据库中收集了 80 例患者的组织。使用既定的评分系统进行免疫组织化学分析和评分。为所有患者和接受辅助化疗的患者生成无复发生存(RFS)和总生存(OS)的 Kaplan-Meier 生存曲线。使用单变量和多变量 Cox 回归分析,结合临床相关协变量,对 MLKL 评分与 RFS 和 OS 进行相关性分析。
患者的中位年龄为 63 岁,53%为男性。低 MLKL 表达与 OS 降低相关(6 个月 vs 17 个月;P=0.006)。在接受辅助化疗的 59 例患者亚组中,低 MLKL 表达与 RFS 降低(5 个月 vs 15 个月;P=0.006)和 OS 降低(6 个月 vs 19 个月;P<0.0001)相关。多变量分析显示,低 MLKL 表达与所有患者的不良 OS 相关(风险比,4.6 [95%置信区间,1.6-13.8];P=0.006)和接受辅助化疗的患者的不良 OS 相关(风险比,8.1 [95%置信区间,2.2-29.2];P=0.002)。
在接受切除术的 PAC 患者中,低 MLKL 表达与 OS 降低相关,在接受切除术的 PAC 患者亚组中,低 MLKL 表达与 RFS 和 OS 降低相关。在 PAC 患者中使用该生物标志物可能提供重要的预后信息。