Chen Bowen, Lei Jin, Zhao Haitao, Dong Jinghui, Zeng Zhen, Li Yinyin, Yu Lingxiang, Zhou Lin, Jia Aiying, Lu Yinying, Cheng Jiamin
Senior Department of Hepatology, The Fifth Medical Center of PLA General Hospital, Beijing, People's Republic of China.
Peking University 302 Clinical Medical School, Beijing, People's Republic of China.
J Hepatocell Carcinoma. 2022 Nov 8;9:1171-1185. doi: 10.2147/JHC.S387254. eCollection 2022.
To explore the efficacy and safety of sorafenib- or lenvatinib-based combination therapy with PD-1 inhibitors in elderly patients aged ≥75 years with unresectable hepatocellular carcinoma (uHCC).
Systemic therapy-naïve uHCC patients who received first-line sorafenib- or lenvatinib-based combination therapy with PD-1 inhibitors were continually reviewed. The primary endpoint was overall survival (OS), and the secondary endpoints were progression-free survival (PFS), objective response rate (ORR), and disease control rate (DCR) in accordance with the Response Evaluation Criteria in Solid Tumors version 1.1. Adverse events (AEs) and immune-related AEs (irAEs) were also evaluated. Groups and subgroups were separated at the ages of 65 and 75 years and compared with 1:1 matching.
Total 169 eligible patients were enrolled, including 24 aged ≥75 years. Median progression-free survival (PFS) and overall survival (OS) in these 24 elderly patients were 4.6 (95% CI: 2.6-6.6) months, and 17.0 (95% CI: 11.2-22.8) months, with 3-, 6-, 12-month OS rate at 82.90%, 73.70%, and 57.50%. Age ≥75 years was confirmed to be a risk factor influencing PFS among patients aged ≥65 years. Adverse events (AEs) were recorded in all these 24 elderly patients, with seven patients experiencing immune-mediated AEs (irAEs). Nearly 30% of elderly patients stopped treatment due to AEs (16% of these due to irAEs). No statistical differences were found in all efficacy endpoints at the cutoff age of 65 years.
For patients aged ≥75 years, application of PD-1 inhibitors in combination with sorafenib or lenvatinib is promising, but this has to be done with caution and needs to be confirmed by future prospective studies.
探讨索拉非尼或仑伐替尼联合PD-1抑制剂治疗≥75岁不可切除肝细胞癌(uHCC)老年患者的疗效和安全性。
对接受一线索拉非尼或仑伐替尼联合PD-1抑制剂治疗、未接受过全身治疗的uHCC患者进行持续评估。主要终点为总生存期(OS),次要终点为无进展生存期(PFS)、客观缓解率(ORR)和疾病控制率(DCR),依据实体瘤疗效评价标准第1.1版进行评估。同时评估不良事件(AE)和免疫相关不良事件(irAE)。按年龄65岁和75岁进行分组和亚组划分,并进行1:1匹配比较。
共纳入169例符合条件的患者,其中24例年龄≥75岁。这24例老年患者的中位无进展生存期(PFS)和总生存期(OS)分别为4.6(95%CI:2.6 - 6.6)个月和17.0(95%CI:11.2 - 22.8)个月,3个月、6个月、12个月的OS率分别为82.90%、73.70%和57.50%。年龄≥75岁被确认为≥65岁患者中影响PFS的危险因素。这24例老年患者均记录到不良事件(AE),7例患者发生免疫介导的不良事件(irAE)。近30%的老年患者因AE停止治疗(其中16%因irAE)。在65岁的分界年龄时,所有疗效终点均未发现统计学差异。
对于≥75岁的患者,PD-1抑制剂联合索拉非尼或仑伐替尼应用前景良好,但必须谨慎使用,且需未来前瞻性研究予以证实。