PMID- 36385419 OWN - NLM STAT- MEDLINE DCOM- 20231023 LR - 20231023 IS - 1591-9528 (Electronic) IS - 1591-8890 (Linking) VI - 23 IP - 6 DP - 2023 Oct TI - Adverse events of immune checkpoint inhibitors in hepatocellular carcinoma: a systemic review and meta-analysis. PG - 2115-2129 LID - 10.1007/s10238-022-00938-6 [doi] AB - The introduction of immune checkpoint inhibitors (ICIs) has reshaped the therapy of hepatocellular carcinoma (HCC). ICIs are a novel therapy with frequent adverse events (AEs), including treatment-related adverse events (trAEs) and immune-related adverse events (irAEs). However, no comprehensive overview of the toxicity spectrum of ICIs in HCC patients has been provided. Electronic databases were searched to identify eligible studies. A meta-analysis of the incidence rate of AEs in HCC patients treated with ICIs was performed. Lastly, the prognostic value of irAEs in HCC patients treated with ICIs was verified. Forty-seven studies with 6472 participations met the inclusion criteria. The pooled all-grade trAEs incidence rate was 83.4% (95% confidence interval [95% CI] 77.0-89.1%), >/= grade 3 trAEs incidence rate was 33.0% (95% CI 26.9-39.5%), all-grade irAEs incidence rate was 34% (95% CI 22-47%), and >/= grade 3 irAEs incidence rate was 9% (95% CI 5-14%). Aspartate aminotransferase (AST) increase (38%, 95% CI 35-40%) is the most common trAEs. Fatigue (14%, 95% CI 7-23%) is the most common irAEs. The pooled results also showed that 18.8% (95% CI 13.2-25.2%) of patients required systemic steroid therapy due to AEs, while 6.6% (95% CI 4.6-9.0%) of patients withdrew from treatment due to AEs. Additionally, patients experiencing irAEs may have a better progression-free survival (PFS) (multivariate analysis: hazard ratio [HR] = 0.41, 95% CI 0.27-0.61, I(2) = 36.3%) but not overall survival (OS) (multivariate analysis: HR = 0.54, 95% CI 0.22-1.36, I(2) = 83.2%) than those with no irAEs. Our study presents a systemic assessment of the AEs profile in HCC patients receiving ICIs, providing important reference for clinicians on toxicity profile. Besides, patients with irAEs may have a better PFS. More large-scale and prospective studies are needed to confirm our conclusions. CI - (c) 2022. The Author(s), under exclusive licence to Springer Nature Switzerland AG. FAU - Tian, Jin-Cheng AU - Tian JC AD - Department of General Surgery, Qilu Hospital of Shandong University, Jinan, China. FAU - Liu, Hui AU - Liu H AD - Department of General Surgery, Qilu Hospital of Shandong University, Jinan, China. FAU - Yan, Lun-Jie AU - Yan LJ AD - Department of General Surgery, Qilu Hospital of Shandong University, Jinan, China. FAU - Ding, Zi-Niu AU - Ding ZN AD - Department of General Surgery, Qilu Hospital of Shandong University, Jinan, China. FAU - Han, Cheng-Long AU - Han CL AD - Department of General Surgery, Qilu Hospital of Shandong University, Jinan, China. FAU - Tian, Bao-Wen AU - Tian BW AD - Department of General Surgery, Qilu Hospital of Shandong University, Jinan, China. FAU - Tan, Si-Yu AU - Tan SY AD - Department of General Surgery, Qilu Hospital of Shandong University, Jinan, China. FAU - Dong, Zhao-Ru AU - Dong ZR AD - Department of General Surgery, Qilu Hospital of Shandong University, Jinan, China. FAU - Wang, Dong-Xu AU - Wang DX AD - Department of General Surgery, Qilu Hospital of Shandong University, Jinan, China. FAU - Xue, Jun-Shuai AU - Xue JS AD - Department of General Surgery, Qilu Hospital of Shandong University, Jinan, China. FAU - Mao, Xin-Cheng AU - Mao XC AD - Department of General Surgery, Qilu Hospital of Shandong University, Jinan, China. FAU - Yan, Yu-Chuan AU - Yan YC AD - Department of General Surgery, Qilu Hospital of Shandong University, Jinan, China. FAU - Li, Tao AU - Li T AD - Department of Hepatobiliary Surgery, The Second Hospital of Shandong University, No. 247 Beiyuan Street, Jinan, 250033, China. litao7706@163.com. LA - eng GR - 82073200 & 81874178/National Natural Science Foundation of China/ GR - 2020GXRC023/Independent Cultivation of Innovative Team from Universities in Jinan/ GR - ZR202105070027/Major basic research of Shandong Provincial Natural Science Foundation/ PT - Journal Article PT - Meta-Analysis PT - Systematic Review DEP - 20221116 PL - Italy TA - Clin Exp Med JT - Clinical and experimental medicine JID - 100973405 RN - 0 (Immune Checkpoint Inhibitors) RN - EC 2.6.1.1 (Aspartate Aminotransferases) SB - IM MH - Humans MH - Immune Checkpoint Inhibitors/adverse effects MH - *Carcinoma, Hepatocellular/drug therapy MH - *Liver Neoplasms/drug therapy MH - Aspartate Aminotransferases OTO - NOTNLM OT - Adverse events OT - Hepatocellular carcinoma OT - Immune checkpoint inhibitors OT - Incidence OT - Meta-analysis OT - Prognosis EDAT- 2022/11/18 06:00 MHDA- 2023/10/23 12:42 CRDT- 2022/11/17 11:01 PHST- 2022/10/09 00:00 [received] PHST- 2022/10/27 00:00 [accepted] PHST- 2023/10/23 12:42 [medline] PHST- 2022/11/18 06:00 [pubmed] PHST- 2022/11/17 11:01 [entrez] AID - 10.1007/s10238-022-00938-6 [pii] AID - 10.1007/s10238-022-00938-6 [doi] PST - ppublish SO - Clin Exp Med. 2023 Oct;23(6):2115-2129. doi: 10.1007/s10238-022-00938-6. Epub 2022 Nov 16.