Frontiers in Oncology (Aug 2022)

PD-L1 expression on circulating tumor cells can be a predictive biomarker to PD-1 inhibitors combined with radiotherapy and antiangiogenic therapy in advanced hepatocellular carcinoma

  • Ke Su,
  • Lu Guo,
  • Kun He,
  • Mingyue Rao,
  • Jianwen Zhang,
  • Xiaoli Yang,
  • Xiaoli Yang,
  • Xiaoli Yang,
  • Weihong Huang,
  • Tao Gu,
  • Ke Xu,
  • Yanlin Liu,
  • Jing Wang,
  • Jiali Chen,
  • Zhenying Wu,
  • Lanxin Hu,
  • Hao Zeng,
  • Hongyan Li,
  • Jian Tong,
  • Xueting Li,
  • Yue Yang,
  • Hanlin Liu,
  • Yaoyang Xu,
  • Zunyuan Tan,
  • Xue Tang,
  • Xunjie Feng,
  • Siyu Chen,
  • Binbin Yang,
  • Hongping Jin,
  • Lechuan Zhu,
  • Bo Li,
  • Bo Li,
  • Bo Li,
  • Yunwei Han,
  • Yunwei Han,
  • Yunwei Han

DOI
https://doi.org/10.3389/fonc.2022.873830
Journal volume & issue
Vol. 12

Abstract

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AimA programmed death 1 (PD-1) inhibitor coupled with radiotherapy and antiangiogenic therapy is a potential therapeutic strategy for advanced hepatocellular carcinoma (HCC). We aimed to determine if circulating tumor cells (CTCs) positive for programmed death-ligand 1 (PD-L1) could be employed as a predictive biomarker in HCC patients receiving triple therapy.MethodsIn this study, HCC patients received a PD-1 inhibitor in combination with intensity-modulated radiotherapy (IMRT) and antiangiogenic therapy. Following IMRT, the PD-1 inhibitor was administrated once every 3 weeks, while the antiangiogenic drug was given once a day. Treatment was continued until the disease progressed. Two mL of peripheral blood was collected at baseline, 1 month, and 3 months after treatment for CTC enrichment using the CytoSorter® system with a CytoSorter™ CTC PD-L1 Kit (Watson Biotech., China).ResultA total of 47 HCC patients receiving the triple therapy were enrolled in this study. Patients with < 2 PD-L1+ CTCs at baseline had a higher objective response rate (ORR) and longer overall survival (OS) than those with ≥ 2 PD-L1+ CTCs (56.5% vs. 16.7%, p = 0.007; not reach vs. 10.8 months, p = 0.001, respectively). The count of PD-L1+ CTCs was found to be an independent predictive biomarker of OS. Furthermore, the objective response was more likely to be achieved in patients with a dynamic decrease in PD-L1+ CTC counts at 1 month after treatment.ConclusionsOur study demonstrated that PD-L1+ CTCs could be a predictive biomarker for HCC patients receiving PD-1 inhibitors in combination with IMRT and antiangiogenic therapy.

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