Tan Yifei, Xu Qing, Wu Zhenru, Zhang Wei, Li Bo, Zhang Bohan, Xu Xi, Zhang Bo, Yan Ke, Song Jiulin, Lv Tao, Yang Jian, Jiang Li, Shi Yujun, Yang Jiayin, Yan Lunan
Department of Liver Surgery, Liver Transplantation Center, West China Hospital of Sichuan University, Chengdu, China.
Institute of Clinical Pathology, Key Laboratory of Transplant Engineering and Immunology, NHC, West China Hospital, Sichuan University, Chengdu, China.
Front Oncol. 2022 Jan 18;11:783335. doi: 10.3389/fonc.2021.783335. eCollection 2021.
The predicting values of programmed cell death protein 1 (PD-1) and programmed death-ligand 1(PD-L1) were unclear in Hepatocellular carcinoma (HCC) patients who receive sorafenib treatment after curative hepatic resection.
We retrospectively enrolled HCC patients who received adjuvant sorafenib treatment after curative resection (N = 154), and patients had resection alone (N = 312). Immunohistochemistry was used to assess expression of PD-1 on tumor infiltration immune cells and PD-L1 on HCC cells. Cox proportional hazard models were used to explore association between clinicopathological factors and risk of tumor recurrence.
No significant difference was detected in RFS (p = 0.542), or OS (p = 0.542) between the resection and sorafenib group and resection alone group. In the 154 patients who received adjuvant sorafenib, expression of PD-1 or PD-L1 was not significantly associated with long-term outcomes. However, in the 122 patients at high risk of postoperative recurrence who had adjuvant sorafenib treatment, characterized by maxim tumor size ≥5 cm, or the presence of macro- or micro-vascular invasion, patients with PD-L1 overexpression (≥3.0) had significantly worse RFS (p = 0.021), and overexpression of PD-L1 (HR: 1.88, 95%CI: 1.18-2.99, p = 0.008) was identified as an independent risk factor associated with unfavorable RFS.
Overexpression of PD-L1 serves as an independent predictor of recurrence in HCC patients at high risk of relapse who received adjuvant sorafenib treatment after curative resection.
在根治性肝切除术后接受索拉非尼治疗的肝细胞癌(HCC)患者中,程序性细胞死亡蛋白1(PD - 1)和程序性死亡配体1(PD - L1)的预测价值尚不清楚。
我们回顾性纳入了根治性切除术后接受辅助索拉非尼治疗的HCC患者(N = 154)以及单纯接受手术切除的患者(N = 312)。采用免疫组织化学法评估肿瘤浸润免疫细胞上PD - 1的表达以及HCC细胞上PD - L1的表达。使用Cox比例风险模型探讨临床病理因素与肿瘤复发风险之间的关联。
切除联合索拉非尼组与单纯切除组之间的无复发生存期(RFS,p = 0.542)或总生存期(OS,p = 0.542)均未检测到显著差异。在154例接受辅助索拉非尼治疗的患者中,PD - 1或PD - L1的表达与长期预后无显著相关性。然而,在122例具有术后复发高风险且接受辅助索拉非尼治疗的患者中,以最大肿瘤直径≥5 cm或存在大血管或微血管侵犯为特征,PD - L1过表达(≥3.0)的患者RFS显著更差(p = 0.021),并且PD - L1过表达(HR:1.88,95%CI:1.18 - 2.99,p = 0.008)被确定为与不良RFS相关的独立危险因素。
PD - L1过表达是根治性切除术后接受辅助索拉非尼治疗的高复发风险HCC患者复发的独立预测因素。