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程序性死亡受体配体1(PD-L1)预测手术切除的局限期小细胞肺癌预后不良。

PD-L1 Predicts Poor Prognosis in Surgically Resected Limited Stage Small-Cell Lung Cancer.

作者信息

Fu Xiao, Liu Zhiyan, Xiang Luochengling, Liu Mengjie, Zheng Xiaoqiang, Wang Jingjing, Liu Na, Gao Huan, Jiang Aimin, Yang Yujuan, Liang Xuan, Ruan Zhiping, Tian Tao, Yao Yu

机构信息

Department of Medical Oncology, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, Shaanxi, 710061, People's Republic of China.

Department of Respiratory and Critical Care Medicine, The Affiliated Hospital of Northwest University, Xi'an No. 3 Hospital, Xi'an, Shaanxi Province, 710018, People's Republic of China.

出版信息

Cancer Manag Res. 2020 Oct 30;12:10939-10948. doi: 10.2147/CMAR.S260599. eCollection 2020.

Abstract

PURPOSE

Small-cell lung cancer (SCLC) is an aggressive high-grade neuroendocrine tumor with limited treatment strategies. Programmed death 1 (PD-1) and its ligand (PD-L1), delta-like ligand-3 (DLL-3), and poly ADP-ribose polymerase (PARP) inhibitors have shed light on the treatment of extensive stage-SCLC. However, the expression and prognostic role of PD-L1, DLL-3, and PARP are barely explored in surgically resected limited stage-SCLC (LS-SCLC).

METHODS

We retrospectively reviewed 404 SCLC patients from 2011 to 2018 in the First Affiliated Hospital of Xi'an Jiaotong University and collected 43 surgically resected LS-SCLC samples with adequate materials and histological specimens containing abundant tumor cells. Immunohistochemistry staining of PD-L1, DLL-3, and PAPR1 was performed by anti-PD-L1 (22C3/Dako), anti-DLL-3, and anti-PAPR1 antibodies, respectively. Positive expression of PD-L1 was characterized as >5% tumor cells and/or tumor-infiltrating immune cells expressing PD-L1. The correlation between PD-L1, DLL-3, PARP1, and clinicopathological characteristics of surgically resected LS-SCLC patients was performed by χ test. The survival curves were calculated by the Kaplan-Meier method and analyzed by the Log rank test and Cox proportional hazards model.

RESULTS AND CONCLUSION

63.04% patients were positive for PD-L1, 65.12% were positive for DLL-3, and 20.93% were positive for PARP1. DLL-3 was significantly overexpressed in SCLC tissues, compared with matched para-noncancerous tissues. Male, elder than 60 years old, advanced TNM stage, smoking, and positive PD-L1 expression predicted shorter DFS, while patients received adjuvant therapy performed better DFS. Further multivariate analysis revealed that TNM stage (HR=2.51, 95% CI=1.31-4.78, =0.005) was an individual prognostic factor for DFS in LS-SCLC. Moreover, advanced TNM stage and positive PD-L1 expression also indicated worse OS, but adjuvant therapy improved OS in LS-SCLC. Multivariate analysis demonstrated that PD-L1 and TNM stage were independent and significant negative predictive factors for OS (HR=2.89, 95% CI=1.21-6.93, =0.017; HR=2.49, 95% CI=1.25-4.94, =0.009 for PD-L1 and TNM stage, respectively), while adjuvant treatment was an independent positive prognostic factor for OS (HR=0.37, 95% CI=0.17-0.81, =0.012).

摘要

目的

小细胞肺癌(SCLC)是一种侵袭性强的高级别神经内分泌肿瘤,治疗策略有限。程序性死亡1(PD-1)及其配体(PD-L1)、δ样配体-3(DLL-3)和聚ADP核糖聚合酶(PARP)抑制剂为广泛期SCLC的治疗带来了新希望。然而,在手术切除的局限期SCLC(LS-SCLC)中,PD-L1、DLL-3和PARP的表达及预后作用鲜少被探讨。

方法

我们回顾性分析了2011年至2018年西安交通大学第一附属医院的404例SCLC患者,并收集了43例手术切除的LS-SCLC样本,这些样本材料充足且组织学标本中含有丰富的肿瘤细胞。分别采用抗PD-L1(22C3/Dako)、抗DLL-3和抗PAPR1抗体对PD-L1、DLL-3和PAPR1进行免疫组化染色。PD-L1阳性表达定义为>5%的肿瘤细胞和/或肿瘤浸润免疫细胞表达PD-L1。采用χ检验分析手术切除的LS-SCLC患者的PD-L1、DLL-3、PARP1与临床病理特征之间的相关性。采用Kaplan-Meier法计算生存曲线,并通过Log rank检验和Cox比例风险模型进行分析。

结果与结论

63.04%的患者PD-L1呈阳性,65.12%的患者DLL-3呈阳性,20.93%的患者PARP1呈阳性。与配对的癌旁组织相比,DLL-3在SCLC组织中显著过表达。男性、年龄大于60岁、TNM分期晚期、吸烟以及PD-L1阳性表达预示无病生存期(DFS)较短,而接受辅助治疗的患者DFS表现较好。进一步多因素分析显示,TNM分期(HR=2.51,95%CI=1.31-4.78,P=0.005)是LS-SCLC患者DFS的独立预后因素。此外,TNM分期晚期和PD-L1阳性表达也提示总生存期(OS)较差,但辅助治疗可改善LS-SCLC患者的OS。多因素分析表明,PD-L1和TNM分期是OS的独立且显著的阴性预测因素(PD-L1和TNM分期的HR分别为2.89,95%CI=1.21-6.93,P=0.017;HR=2.49,95%CI=1.25-4.94,P=0.009),而辅助治疗是OS的独立阳性预后因素(HR=0.37,95%CI=0.17-0.81,P=0.012)

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0201/7608588/2c22f33f246c/CMAR-12-10939-g0001.jpg

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