Division of Gastroenterology and Hepatology, Department of Internal Medicine III, Medical University of Vienna, Vienna, Austria.
Liver Cancer (HCC) Study Group Vienna, Division of Gastroenterology and Hepatology, Department of Internal Medicine III, Medical University of Vienna, Vienna, Austria.
United European Gastroenterol J. 2024 Oct;12(8):1034-1043. doi: 10.1002/ueg2.12626. Epub 2024 Jul 11.
Deterioration of liver function is a leading cause of death in patients with advanced hepatocellular carcinoma (HCC). We evaluated the impact of immune checkpoint inhibitor (ICI)-treatment on liver function and outcomes.
HCC patients receiving ICIs or sorafenib between 04/2003 and 05/2024 were included. Liver function (assessed by Child-Pugh score [CPS]) was evaluated at the start of ICI-treatment (baseline, BL) and 3 and 6 months thereafter. A ≥1 point change in CPS was defined as deterioration (-) or improvement (+), while equal CPS points were defined as stable (=).
Overall, 182 ICI-treated patients (66.8 ± 11.8 years; cirrhosis: n = 134, 74%) were included. At BL, median CPS was 5 (IQR: 5-6; CPS-A: 147, 81%). After 3 months, liver function improved/stabilized in 102 (56%) and deteriorated in 61 (34%) patients, while 19 (10%) patients deceased/had missing follow-up (d/noFU). Comparable results were observed at 6 months (+/=: n = 82, 45%; -: n = 55, 30%; d/noFU: n = 45, 25%). In contrast, 54 (34%) and 33 (21%) out of 160 sorafenib patients achieved improvement/stabilization at 3 and 6 months, respectively. Radiological response was linked to CPS improvement/stabilization at 6 months (responders vs. non-responders, 73% vs. 50%; p = 0.007). CPS improvement/stabilization at 6 months was associated with better overall survival following landmark analysis (6 months: +/=: 28.4 [95% CI: 18.7-38.1] versus -: 14.2 [95% CI: 10.3-18.2] months; p < 0.001). Of 35 ICI-patients with CPS-B at BL, improvement/stabilization occurred in 16 (46%) patients, while 19 (54%) patients deteriorated/d/noFU at 3 months. Comparable results were observed at 6 months (CPS +/=: 14, 40%, -: 8, 23%). Importantly, 6/35 (17%) and 9/35 (26%) patients improved from CPS-B to CPS-A at 3 and 6 months.
Radiological response to ICI-treatment was associated with stabilization or improvement in liver function, which correlated with improved survival, even in patients with Child-Pugh class B at baseline.
肝功能恶化是晚期肝细胞癌(HCC)患者死亡的主要原因。我们评估了免疫检查点抑制剂(ICI)治疗对肝功能和结局的影响。
纳入 2003 年 4 月至 2024 年 5 月期间接受 ICI 或索拉非尼治疗的 HCC 患者。ICI 治疗开始时(基线,BL)和此后 3 个月和 6 个月评估肝功能(通过 Child-Pugh 评分[CPS]评估)。CPS 至少增加 1 分定义为恶化(-)或改善(+),而 CPS 相等定义为稳定(=)。
共纳入 182 例接受 ICI 治疗的患者(66.8±11.8 岁;肝硬化:n=134,74%)。BL 时,中位 CPS 为 5(IQR:5-6;CPS-A:147,81%)。3 个月后,102 例(56%)患者的肝功能改善/稳定,61 例(34%)患者的肝功能恶化,19 例(10%)患者死亡/无随访(d/noFU)。6 个月时观察到类似的结果(+/=:n=82,45%;-:n=55,30%;d/noFU:n=45,25%)。相比之下,160 例索拉非尼患者中有 54 例(34%)和 33 例(21%)在 3 个月和 6 个月时分别达到改善/稳定。6 个月时的影像学反应与 CPS 改善/稳定相关(应答者与无应答者,73%与 50%;p=0.007)。6 个月时 CPS 改善/稳定与 landmark 分析后的总生存更好相关(6 个月:+/=:28.4[95%CI:18.7-38.1]vs.-:14.2[95%CI:10.3-18.2]个月;p<0.001)。在基线时 CPS-B 的 35 例 ICI 患者中,16 例(46%)患者出现改善/稳定,而 19 例(54%)患者在 3 个月时恶化/d/noFU。6 个月时观察到类似的结果(+/=:14,40%,-:8,23%)。重要的是,6/35(17%)和 9/35(26%)患者在 3 个月和 6 个月时从 CPS-B 改善为 CPS-A。
ICI 治疗的影像学反应与肝功能的稳定或改善相关,这与生存改善相关,即使在基线时 CPS 为 B 级的患者中也是如此。