Kudo Masatoshi, Galle Peter R, Llovet Josep M, Finn Richard S, Vogel Arndt, Motomura Kenta, Assenat Eric, Merle Philippe, Brandi Giovanni, Daniele Bruno, Okusaka Takuji, Tomášek Jiří, Borg Christophe, Dadduzio Vincenzo, Morimoto Manabu, Pracht Marc, Jen Min-Hua, Drove Ubreva Nora, Widau Ryan C, Shinozaki Kenta, Yoshikawa Reigetsu, Zhu Andrew X
Department of Gastroenterology and Hepatology, Kindai University Faculty of Medicine, Osaka, Japan.
Department of Internal Medicine, Mainz University Medical Center, Mainz, Germany.
Liver Int. 2020 Aug;40(8):2008-2020. doi: 10.1111/liv.14462. Epub 2020 May 6.
BACKGROUND & AIMS: Limited data on treatment of elderly patients with hepatocellular carcinoma (HCC) increase the unmet need. REACH and REACH-2 were global phase III studies of ramucirumab in patients with HCC after prior sorafenib, where patients with alpha-fetoprotein (AFP) ≥400 ng/mL showed an overall ssurvival (OS) benefit for ramucirumab. These post-hoc analyses examined efficacy and safety of ramucirumab in patients with HCC and baseline AFP ≥ 400 ng/mL by three prespecified age subgroups (<65, ≥65 to <75 and ≥75 years).
Individual patient data were pooled from REACH (baseline AFP ≥400 ng/mL) and REACH-2. Kaplan-Meier and Cox proportional hazards regression methods (stratified by study) assessed OS, progression-free survival (PFS), time to progression (TTP) and patient-reported outcomes (Functional Hepatobiliary System Index-8 [FHSI-8] score).
A total of 542 patients (<65 years: n = 302; ≥65 to <75 years: n = 160; ≥75 years: n = 80) showed similar baseline characteristics between ramucirumab and placebo. Older subgroups had higher hepatitis C and steatohepatitis incidences, and lower AFP levels, than the <65 years subgroup. Ramucirumab prolonged OS in patients <65 years (hazard ratio [HR], 0.753; 95% CI 0.581-0.975), ≥65 to <75 years (0.602; 0.419-0.866) and ≥75 years (0.709; 0.420-1.199), PFS and TTP irrespective of age. Ramucirumab showed similar overall safety profiles across subgroups, with a consistent median relative dose intensity ≥97.8%. A trend towards a delay in symptom deterioration in FHSI-8 with ramucirumab was observed in all subgroups.
In this post-hoc analysis, ramucirumab showed a survival benefit across age subgroups with a tolerable safety profile, supporting its use in advanced HCC with elevated AFP, irrespective of age, including ≥75 years.
关于老年肝细胞癌(HCC)患者治疗的数据有限,这增加了未满足的需求。REACH和REACH-2是在既往使用索拉非尼治疗后的HCC患者中进行的雷莫西尤单抗全球III期研究,其中甲胎蛋白(AFP)≥400 ng/mL的患者显示雷莫西尤单抗可带来总生存期(OS)获益。这些事后分析通过三个预先设定的年龄亚组(<65岁≥65至<75岁以及≥75岁)研究了雷莫西尤单抗在基线AFP≥400 ng/mL的HCC患者中的疗效和安全性。
汇总来自REACH(基线AFP≥400 ng/mL)和REACH-2的个体患者数据。采用Kaplan-Meier法和Cox比例风险回归方法(按研究分层)评估OS、无进展生存期(PFS)、疾病进展时间(TTP)以及患者报告结局(功能性肝胆系统指数-8 [FHSI-8]评分)。
共有542例患者(<65岁:n = 302;≥65至<75岁:n = 160;≥75岁:n = 80),雷莫西尤单抗组和安慰剂组的基线特征相似。与<65岁亚组相比,年龄较大的亚组丙型肝炎和脂肪性肝炎发病率更高,AFP水平更低。雷莫西尤单抗延长了<65岁患者(风险比[HR],0.753;95% CI 0.581-0.975)、≥65至<75岁患者(0.602;0.419-0.866)以及≥75岁患者(0.709;0.420-1.199)的OS、PFS和TTP(与年龄无关)。雷莫西尤单抗在各亚组中的总体安全性相似,中位相对剂量强度持续≥97.8%。在所有亚组中均观察到雷莫西尤单抗使FHSI-8症状恶化出现延迟的趋势。
在此事后分析中,雷莫西尤单抗在各年龄亚组中均显示出生存获益,且安全性可耐受,支持其用于AFP升高的晚期HCC患者,无论年龄大小,包括≥75岁的患者。