Hu Zili, Yang Zhoutian, Fu Zibo, Fu Yizhen, Ma Zeliang, Zhou Zhongguo, Chen Minshan, Zhang Yaojun
Department of Liver Surgery, Sun Yat-Sen University Cancer Center, Guangzhou, China.
Collaborative Innovation Center for Cancer Medicine, State Key Laboratory of Oncology in South China, Sun Yat-Sen University Cancer Center, Guangzhou, China.
Front Immunol. 2024 Nov 19;15:1472870. doi: 10.3389/fimmu.2024.1472870. eCollection 2024.
The relative superiority of atezolizumab-bevacizumab versus pembrolizumab-lenvatinib in treatment of unresectable hepatocellular carcinoma (HCC) remains uncertain. This study aims to compare the efficacy of atezolizumab-bevacizumab and pembrolizumab-lenvatinib in first-line treatments for unresectable HCC.
A total of 72 patients receiving pembrolizumab-lenvatinib (PL group) and 92 patients receiving atezolizumab-bevacizumab (AB group) between January 2019 and June 2023 were included in this study. By employing propensity score matching (PSM), we compared the overall survival (OS) and progression-free survival (PFS) between the two groups.
After PSM, the 1-, 2-, and 3-year OS rates were 70.4%, 54.5%, and 40.0% in the PL group, and 88.4%, 44.2%, and 44.2% in the AB group, respectively. The 6-, 12-, and 18-month PFS rates were 56.9%, 43.0%, and 32.1% in the PL group, and 74.2%, 40.9%, and 30.7% in the AB group, respectively. No significant differences were observed in both OS (HR, 0.498; 95% CI, 0.217-1.143; = 0.1) and PFS (HR, 0.913; 95% CI, 0.512-0.1.629; = 0.758) between the two groups. Through subgroup analysis, we developed a Cirrhosis-Portal vein invasion-ALBI (CPA) score and identified that the AB group exhibited significantly longer OS than the PL group in the CPA high population (HR, 0.219; 95% CI, 0.075-0.637; = 0.005). The treatment-related adverse events between the PL group and the AB group were comparable.
This study suggests that the efficacy of pembrolizumab-lenvatinib and atezolizumab-bevacizumab is comparable in first-line treatment of unresectable HCC, the atezolizumab-bevacizumab combination may confer additional benefits for patients with high CPA scores compared to pembrolizumab-lenvatinib.
阿替利珠单抗联合贝伐珠单抗与帕博利珠单抗联合乐伐替尼在治疗不可切除肝细胞癌(HCC)方面的相对优势仍不确定。本研究旨在比较阿替利珠单抗联合贝伐珠单抗与帕博利珠单抗联合乐伐替尼在不可切除HCC一线治疗中的疗效。
本研究纳入了2019年1月至2023年6月期间共72例接受帕博利珠单抗联合乐伐替尼治疗(PL组)的患者和92例接受阿替利珠单抗联合贝伐珠单抗治疗(AB组)的患者。通过倾向评分匹配(PSM),我们比较了两组之间的总生存期(OS)和无进展生存期(PFS)。
PSM后,PL组1年、2年和3年的OS率分别为70.4%、54.5%和40.0%,AB组分别为88.4%、44.2%和44.2%。PL组6个月、12个月和18个月的PFS率分别为56.9%、43.0%和32.1%,AB组分别为74.2%、40.9%和30.7%。两组在OS(HR,0.498;95%CI,0.217 - 1.143;P = 0.1)和PFS(HR,0.913;95%CI,0.512 - 1.629;P = 0.758)方面均未观察到显著差异。通过亚组分析,我们制定了肝硬化-门静脉侵犯-白蛋白-胆红素(CPA)评分,并确定在CPA高分组中,AB组的OS明显长于PL组(HR,0.219;95%CI,0.075 - 0.637;P = 0.005)。PL组和AB组之间的治疗相关不良事件具有可比性。
本研究表明,帕博利珠单抗联合乐伐替尼与阿替利珠单抗联合贝伐珠单抗在不可切除HCC的一线治疗中疗效相当,与帕博利珠单抗联合乐伐替尼相比,阿替利珠单抗联合贝伐珠单抗组合可能为CPA评分高的患者带来额外益处。