Department of Oncology and Hematology, San Martino Hospital, Oristano, Italy.
Department of Oncology, Vita-Salute San Raffaele University, IRCCS San Raffaele Scientific Institute Hospital, via Olgettina 60, 20132, Milan, Italy.
Target Oncol. 2024 Jan;19(1):29-39. doi: 10.1007/s11523-023-01029-6. Epub 2024 Jan 22.
BACKGROUND: Data concerning the use of lenvatinib in very old patients (≥ 80 years) are limited, although the incidence of hepatocellular carcinoma (HCC) in this patient population is constantly increasing. OBJECTIVE: This analysis aimed to evaluate the efficacy and safety of lenvatinib in a large cohort of very old patients (≥ 80 years) with unresectable HCC. PATIENTS AND METHODS: The study was conducted on a cohort of 1325 patients from 46 centers in four Western and Eastern countries (Italy, Germany, Japan, and the Republic of Korea) who were undergoing first-line treatment with lenvatinib between July 2010 and February 2022. Patients were stratified according to age as very old (≥ 80 years) and not very old (< 80 years). RESULTS: The median overall survival (OS) was 15.7 months for patients < 80 years old and 18.4 months for patients ≥ 80 years old [hazard ratio (HR) = 1.02, 95% confidence interval (CI) 0.84-1.25, p = 0.8281]. Median progression free survival (PFS) was 6.3 months for patients < 80 years old and 6.5 months for patients ≥ 80 years old (HR = 1.07, 95% CI 0.91-1.25, p = 0.3954). No differences between the two study groups were found in terms of disease control rate (DCR; 80.8% versus 78.8%; p = 0.44) and response rate (RR; 38.2% versus 37.9%; p = 0.88). Patients < 80 years old experienced significantly more hand-foot skin reaction (HFSR) grade ≥ 2 and decreased appetite grade ≥ 2. Conversely, patients ≥ 80 years old experienced significantly more fatigue grade ≥ 2. In the very old group, parameters associated with prognosis were AFP, albumin-bilirubin (ALBI) grade, Barcelona Clinic Liver Cancer (BCLC), and Child-Pugh score. BCLC stage was the only independent predictor of overall survival (OS; HR = 1.59, 95% CI 1.11-2.29, p = 0.01115). CONCLUSIONS: Our study highlights the same efficacy and safety of lenvatinib between very old and not very old patients.
背景:关于仑伐替尼在非常高龄(≥80 岁)患者中的应用数据有限,尽管此类患者人群中的肝细胞癌(HCC)发病率一直在持续上升。
目的:本分析旨在评估仑伐替尼在来自四个西方国家和一个东方国家(意大利、德国、日本和韩国)的 46 个中心的大量非常高龄(≥80 岁)不可切除 HCC 患者中的疗效和安全性。
患者和方法:该研究纳入了 1325 例患者,他们在 2010 年 7 月至 2022 年 2 月期间接受仑伐替尼一线治疗,这些患者来自于上述 4 个国家的 46 个中心。患者根据年龄分为非常高龄(≥80 岁)和非非常高龄(<80 岁)。
结果:<80 岁患者的中位总生存期(OS)为 15.7 个月,≥80 岁患者的中位 OS 为 18.4 个月[风险比(HR)=1.02,95%置信区间(CI)0.84-1.25,p=0.8281]。<80 岁患者的中位无进展生存期(PFS)为 6.3 个月,≥80 岁患者的中位 PFS 为 6.5 个月(HR=1.07,95%CI 0.91-1.25,p=0.3954)。两组之间的疾病控制率(DCR;80.8% vs. 78.8%;p=0.44)和缓解率(RR;38.2% vs. 37.9%;p=0.88)无差异。<80 岁患者发生≥2 级手足皮肤反应(HFSR)和≥2 级食欲下降的比例显著更高,而≥80 岁患者发生≥2 级乏力的比例显著更高。在非常高龄组中,与预后相关的参数包括 AFP、白蛋白-胆红素(ALBI)分级、巴塞罗那临床肝癌(BCLC)和 Child-Pugh 评分。BCLC 分期是总生存期(OS)的唯一独立预测因素(HR=1.59,95%CI 1.11-2.29,p=0.01115)。
结论:本研究表明仑伐替尼在非常高龄和非非常高龄患者中的疗效和安全性相当。
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