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不可切除肝细胞癌患者接受仑伐替尼治疗时间较长的特征:日本上市后监测研究的事后分析。

Characteristics of patients with longer treatment period of lenvatinib for unresectable hepatocellular carcinoma: A post-hoc analysis of post-marketing surveillance study in Japan.

机构信息

Department of Gastroenterology, Kanazawa University Hospital, Kanazawa, Japan.

Eisai Co., Ltd., Tokyo, Japan.

出版信息

PLoS One. 2024 Mar 8;19(3):e0298420. doi: 10.1371/journal.pone.0298420. eCollection 2024.

DOI:10.1371/journal.pone.0298420
PMID:38457389
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10923456/
Abstract

Patient profiles suitable for long-term lenvatinib treatment for unresectable hepatocellular carcinoma (uHCC) are yet to be fully understood. This post-hoc analysis aimed to identify such patient characteristics and explore the impact of treatment duration and relative dose intensity (RDI) on treatment outcomes. The data were obtained from 703 patients in a multicenter, prospective cohort study in Japan. Lenvatinib-naïve patients with uHCC were enrolled between July 2018 and January 2019 and were followed up for 12 months. Moreover, patients were dichotomized using the median treatment duration into the longer- (≥177 days; n = 352) or shorter-treatment (<177 days; n = 351) groups. The longer-treatment group often had better performance status, lower Child-Pugh score and better modified albumin-bilirubin grade than the shorter treatment group (p<0.05 for all). The objective response rate (47.6% vs. 28.2%; p<0.001) and disease control rate (92.4% vs. 60.2%; p<0.001) were both significantly higher in the longer-treatment groups than in the shorter-treatment groups. The proportion of patients with any adverse drug reactions was generally similar between the two treatment groups. Within the longer-treatment group, the disease control rate was high regardless of dose modification (i.e., RDI <100% vs. ≥100% during the initial 177 days) (91.2% vs. 98.0%). In conclusion, patients with longer treatment tended to have better overall conditions. Lenvatinib dose modifications at the physician's discretion, considering the balance between effectiveness and safety, may contribute to the long-term treatment.

摘要

适合不可切除肝细胞癌(uHCC)长期仑伐替尼治疗的患者特征尚未完全明确。本回顾性分析旨在确定这些患者特征,并探讨治疗持续时间和相对剂量强度(RDI)对治疗结果的影响。该数据来自日本多中心前瞻性队列研究中的 703 例患者。2018 年 7 月至 2019 年 1 月期间,招募了仑伐替尼初治的 uHCC 患者,并随访 12 个月。此外,将患者按治疗持续时间的中位数分为较长治疗组(≥177 天;n = 352)或较短治疗组(<177 天;n = 351)。较长治疗组的患者表现状态更好,Child-Pugh 评分更低,改良白蛋白-胆红素分级更好,这些情况均优于较短治疗组(所有 P 值均<0.05)。较长治疗组的客观缓解率(47.6% vs. 28.2%;P<0.001)和疾病控制率(92.4% vs. 60.2%;P<0.001)均显著高于较短治疗组。两组患者发生任何药物不良反应的比例大致相似。在较长治疗组内,无论剂量调整情况如何(即最初 177 天内 RDI<100%与≥100%),疾病控制率均较高(91.2% vs. 98.0%)。总之,接受较长治疗的患者总体状况较好。仑伐替尼剂量的调整应由医生根据疗效和安全性的平衡来决定,这可能有助于长期治疗。

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本文引用的文献

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Clinical Practice Guidelines for Hepatocellular Carcinoma: The Japan Society of Hepatology 2021 version (5th JSH-HCC Guidelines).肝细胞癌临床实践指南:日本肝脏学会2021版(第5版JSH-HCC指南)
Hepatol Res. 2023 May;53(5):383-390. doi: 10.1111/hepr.13892. Epub 2023 Mar 10.
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Safety and Effectiveness of Lenvatinib in Patients with Unresectable Hepatocellular Carcinoma in Real-World Clinical Practice: An Observational Post-Marketing Study in Japan.在现实临床实践中,乐伐替尼用于不可切除肝细胞癌患者的安全性和有效性:日本一项上市后观察性研究
Drugs Real World Outcomes. 2023 Jun;10(2):195-205. doi: 10.1007/s40801-022-00348-w. Epub 2023 Jan 5.
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Overall survival and objective response in advanced unresectable hepatocellular carcinoma: A subanalysis of the REFLECT study.
晚期不可切除肝细胞癌的总生存期和客观缓解率:REFLECT研究的亚组分析
J Hepatol. 2023 Jan;78(1):133-141. doi: 10.1016/j.jhep.2022.09.006. Epub 2022 Sep 20.
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Influence of skeletal muscle volume loss during lenvatinib treatment on prognosis in unresectable hepatocellular carcinoma: a multicenter study in Tohoku, Japan.仑伐替尼治疗期间骨骼肌容积丢失对不可切除肝细胞癌预后的影响:日本东北地区的一项多中心研究。
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Evolution of Survival Impact of Molecular Target Agents in Patients with Advanced Hepatocellular Carcinoma.分子靶向药物对晚期肝细胞癌患者生存影响的演变
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