Department of Surgery & Cancer, Imperial College London, Hammersmith Hospital, London, UK.
Department of Biomedical Sciences, Humanitas University, Pieve Emanuele, Italy.
Liver Int. 2022 Nov;42(11):2538-2547. doi: 10.1111/liv.15405. Epub 2022 Sep 2.
Combination atezolizumab/bevacizumab is the gold standard for first-line treatment of unresectable hepatocellular carcinoma (HCC). Our study investigated the efficacy and safety of combination therapy in older patients with HCC.
191 consecutive patients from eight centres receiving atezolizumab and bevacizumab were included. Overall survival (OS), progression-free survival (PFS), overall response rate (ORR) and disease control rate (DCR) defined by RECIST v1.1 were measured in older (age ≥ 65 years) and younger (age < 65 years) age patients. Treatment-related adverse events (trAEs) were evaluated.
The elderly (n = 116) had higher rates of non-alcoholic fatty liver disease (19.8% vs. 2.7%; p < .001), presenting with smaller tumours (6.2 cm vs 7.9 cm, p = .02) with less portal vein thrombosis (31.9 vs. 54.7%, p = .002), with fewer patients presenting with BCLC-C stage disease (50.9 vs. 74.3%, p = .002). There was no significant difference in OS (median 14.9 vs. 15.1 months; HR 1.15, 95% CI 0.65-2.02 p = .63) and PFS (median 7.1 vs. 5.5 months; HR 1.11, 95% CI 0.54-1.92; p = .72) between older age and younger age. Older patients had similar ORR (27.6% vs. 20.0%; p = .27) and DCR (77.5% vs. 66.1%; p = .11) compared to younger patients. Atezolizumab-related (40.5% vs. 48.0%; p = .31) and bevacizumab-related (44.8% vs. 41.3%; p = .63) trAEs were comparable between groups. Rates of grade ≥3 trAEs and toxicity-related treatment discontinuation were similar between older and younger age patients. Patients 75 years and older had similar survival and safety outcomes compared to younger patients.
Atezolizumab and bevacizumab therapy is associated with comparable efficacy and tolerability in older age patients with unresectable HCC.
阿替利珠单抗联合贝伐珠单抗是不可切除肝细胞癌(HCC)一线治疗的金标准。我们的研究旨在调查阿替利珠单抗联合贝伐珠单抗在老年 HCC 患者中的疗效和安全性。
纳入了来自 8 个中心的 191 例连续接受阿替利珠单抗和贝伐珠单抗治疗的患者。在年龄≥65 岁(老年组)和年龄<65 岁(年轻组)的患者中,分别评估总生存期(OS)、无进展生存期(PFS)、总缓解率(ORR)和疾病控制率(DCR)。根据 RECIST v1.1 标准,评估治疗相关不良事件(trAEs)。
老年组(n=116)非酒精性脂肪性肝病(NAFLD)发生率较高(19.8% vs. 2.7%;p<.001),肿瘤较小(6.2cm vs. 7.9cm,p=0.02),门静脉血栓形成较少(31.9% vs. 54.7%,p=0.002),BCLC-C 期疾病患者较少(50.9% vs. 74.3%,p=0.002)。老年组和年轻组之间 OS(中位 14.9 个月 vs. 15.1 个月;HR 1.15,95%CI 0.65-2.02;p=0.63)和 PFS(中位 7.1 个月 vs. 5.5 个月;HR 1.11,95%CI 0.54-1.92;p=0.72)均无显著差异。与年轻组相比,老年组 ORR(27.6% vs. 20.0%;p=0.27)和 DCR(77.5% vs. 66.1%;p=0.11)相似。阿替利珠单抗相关(40.5% vs. 48.0%;p=0.31)和贝伐珠单抗相关(44.8% vs. 41.3%;p=0.63)trAEs 在两组间相似。≥3 级 trAEs 发生率和因毒性相关停药率在老年组和年轻组间相似。75 岁及以上患者的生存和安全性结局与年轻患者相似。
阿替利珠单抗联合贝伐珠单抗治疗不可切除 HCC 的疗效和耐受性在老年患者中相似。