Ziogas Ioannis A, Evangeliou Alexandros P, Giannis Dimitrios, Hayat Muhammad H, Mylonas Konstantinos S, Tohme Samer, Geller David A, Elias Nahel, Goyal Lipika, Tsoulfas Georgios
First Department of Surgery, Aristotle University of Thessaloniki, Thessaloniki, Greece.
Surgery Working Group, Society of Junior Doctors, Athens, Greece.
Oncologist. 2021 Jun;26(6):e1036-e1049. doi: 10.1002/onco.13638. Epub 2021 Jan 2.
Immune checkpoints inhibitors (ICIs) have emerged as a treatment option for several malignancies. Nivolumab, pembrolizumab, nivolumab plus ipilimumab, and atezolizumab plus bevacizumab have been approved for the management of advanced-stage hepatocellular carcinoma (HCC). We aimed to systematically review the literature and summarize the characteristics and outcomes of patients with HCC treated with ICIs.
A systematic literature search of PubMed, the Cochrane Library, and ClinicalTrials.gov was performed according to the PRISMA statement (end of search date: November 7, 2020). Quality of evidence assessment was also performed.
Sixty-three articles including 2,402 patients were analyzed, 2,376 of whom received ICIs for unresectable HCC. Response to ICIs could be evaluated in 2,116 patients; the overall objective response rate (ORR) and disease control rate (DCR) were 22.7% and 60.7%, respectively, and the mean overall survival (OS) was 15.8 months. The ORR, DCR, and OS for nivolumab (n = 846) were 19.7%, 51.1%, and 18.7 months, respectively; for pembrolizumab (n = 435) they were 20.7%, 64.6% and 13.3 months, respectively. The combination of atezolizumab/bevacizumab (n = 460) demonstrated an ORR and DCR of 30% and 77%, respectively. The overall rate of treatment discontinuation because of adverse events was 14.9%. Fifteen patients received ICIs in the liver transplant (LT) setting (one pre-LT for bridging, 14 for post-LT recurrence); fatal graft rejection was reported in 40.0% (n = 6/15) and mortality in 80.0% (n = 12/15).
ICIs are safe and effective against unresectable HCC, but caution is warranted regarding their use in the LT setting because of the high graft rejection rate.
This systematic review pooled the outcomes from studies reporting on the use of immune checkpoint inhibitors (ICIs) for the management of 2,402 patients with advanced-stage hepatocellular carcinoma (HCC), 2,376 of whom had unresectable HCC. The objective response rate and disease control rate were 22.7% and 60.7%, respectively, and the mean overall survival was 15.8 months. The overall rate of treatment discontinuation because of adverse events was 14.9%. Fifteen patients received ICIs in the liver transplant (LT) setting (one pre-LT for bridging, 14 for post-LT recurrence). Six of these patients experienced graft rejection (40.0%).
免疫检查点抑制剂(ICIs)已成为多种恶性肿瘤的一种治疗选择。纳武利尤单抗、帕博利珠单抗、纳武利尤单抗联合伊匹木单抗以及阿替利珠单抗联合贝伐珠单抗已被批准用于晚期肝细胞癌(HCC)的治疗。我们旨在系统回顾文献并总结接受ICIs治疗的HCC患者的特征和治疗结果。
根据PRISMA声明(检索截止日期:2020年11月7日),对PubMed、Cochrane图书馆和ClinicalTrials.gov进行系统的文献检索。同时还进行了证据质量评估。
分析了63篇文章,共2402例患者,其中2376例接受ICIs治疗不可切除的HCC。2116例患者可评估对ICIs的反应;总体客观缓解率(ORR)和疾病控制率(DCR)分别为22.7%和60.7%,平均总生存期(OS)为15.8个月。纳武利尤单抗(n = 846)的ORR、DCR和OS分别为19.7%、51.1%和18.7个月;帕博利珠单抗(n = 435)的分别为20.7%、64.6%和13.3个月。阿替利珠单抗/贝伐珠单抗联合治疗(n = 460)的ORR和DCR分别为30%和77%。因不良事件导致治疗中断的总体发生率为14.9%。15例患者在肝移植(LT)情况下接受ICIs治疗(1例在LT前用于桥接,14例在LT后复发);报告有40.0%(n = 6/15)发生致命性移植物排斥反应,80.0%(n = 12/15)死亡。
ICIs对不可切除的HCC安全有效,但由于移植物排斥率高,在LT情况下使用时需谨慎。
本系统评价汇总了关于使用免疫检查点抑制剂(ICIs)治疗2402例晚期肝细胞癌(HCC)患者的研究结果,其中2376例为不可切除的HCC。客观缓解率和疾病控制率分别为22.7%和60.7%,平均总生存期为15.8个月。因不良事件导致治疗中断的总体发生率为14.9%。15例患者在肝移植(LT)情况下接受ICIs治疗(1例在LT前用于桥接,14例在LT后复发)。其中6例患者发生移植物排斥反应(40.0%)。