Department of Hepatobiliary Surgery, The First Affiliated Hospital of Chongqing Medical University, Chongqing 400016, China.
Curr Cancer Drug Targets. 2020;20(9):720-727. doi: 10.2174/1568009620666200520084415.
Immune checkpoint modulators, such as the programmed death protein-1 (PD-1)/programmed death ligand-1 (PD-L1) inhibitor, cytotoxic T-Lymphocyte-associated antigen 4 (CTLA-4) inhibitor have been investigated with encouraging results for hepatocellular carcinoma (HCC). However, the safety of this strategy in patients with previous liver transplantation (LT) is not well studied.
To explore the safety and feasibility of immune checkpoints inhibitors in recurrent and metastatic HCC patients on a background of LT.
A case of recurrent, refractory, metastatic HCC after LT, where PD-1 inhibitor was initiated, was described and related literature was reviewed.
There was complete remission in lung metastases and the partial radiological response of metastatic retroperitoneal lymph node to the drug with no liver graft rejection after 13 cycles of PD- 1 inhibitor injection. PD-1inhibitor, at least in this patient, was verified to play an important role in controlling tumor progression and prolonging patient survival.
This novel drug might be a useful method to allow doctors to guarantee a better chance for long-term survival in recurrent, metastatic HCC patients with the previous LT. However, it should be used with caution in allograft recipients due to the risk of acute graft rejection, further larger, prospective studies are needed to determine optimal immunomodulatory therapy to achieve optimal anti-tumor efficacy with transplant liver preservation.
免疫检查点调节剂,如程序性死亡蛋白-1(PD-1)/程序性死亡配体-1(PD-L1)抑制剂、细胞毒性 T 淋巴细胞相关抗原 4(CTLA-4)抑制剂,已被研究用于治疗肝细胞癌(HCC),并取得了令人鼓舞的结果。然而,这种策略在肝移植(LT)后患者中的安全性尚未得到充分研究。
探讨免疫检查点抑制剂在 LT 背景下复发和转移性 HCC 患者中的安全性和可行性。
描述了一例 LT 后复发、难治、转移性 HCC 患者开始使用 PD-1 抑制剂的病例,并复习了相关文献。
在 13 个周期的 PD-1 抑制剂注射后,肺部转移灶完全缓解,转移性腹膜后淋巴结的部分影像学反应对药物有反应,肝移植物无排斥反应。PD-1 抑制剂至少在这名患者中被证实对控制肿瘤进展和延长患者生存具有重要作用。
对于 LT 后复发和转移性 HCC 患者,这种新型药物可能是一种有用的方法,可以保证他们有更好的长期生存机会。然而,由于急性移植物排斥的风险,在同种异体受者中应谨慎使用,需要进一步进行更大规模的前瞻性研究,以确定最佳的免疫调节治疗方法,以在保留移植肝的情况下实现最佳的抗肿瘤疗效。