Lenvatinib in advanced thyroid, salivary gland, endometrial, and hepatocellular carcinomas: a real-world study on treatment duration and toxicity management.

IF 4.2 2区 医学 Q2 ONCOLOGY
Therapeutic Advances in Medical Oncology Pub Date : 2025-09-12 eCollection Date: 2025-01-01 DOI:10.1177/17588359251359905
Elena Colombo, Monika Ducceschi, Stefano Cavalieri, Maggie Polignano, Marta Bini, Paolo Ambrosini, Matteo De Monte, Giulia Montelatici, Alessandra Russo, Valentina Bellia, Sharrie Bhoori, Cristiana Bergamini, Salvatore Alfieri, Imperia Nuzzolese, Arianna Ottini, Vincenzo Mazzaferro, Francesco Raspagliesi, Lisa Licitra, Mara Mantiero
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引用次数: 0

Abstract

Background: Lenvatinib (LEN) is a multikinase inhibitor used for different tumors: advanced differentiated thyroid cancers progressed or resistant to radioiodine (RAIR DTC), adenoid cystic carcinoma of salivary glands (AdCC), hepatocellular carcinoma (HCC), and endometrial carcinoma (EC). In the real-world setting, patients eligible for LEN often have multiple comorbidities and/or impaired Eastern Cooperative Oncology Group performance status (ECOG PS). In HCC, patients with body weight (BW) < 60 kg require a low starting dose of LEN; in thyroid cancers (TC), BW has a clinically relevant effect on steady-state exposure to LEN. It is currently unknown whether BW can vary during LEN treatment across different histologies.

Objectives: This study aims to investigate toxicities, duration of treatment (DoT), and to describe BW and body mass index (BMI) intrapatient variations in the real-world setting.

Design: Retrospective observational study conducted in a tertiary cancer center.

Methods: We collected clinical features and AEs from consecutive adult patients who started LEN for DTC, AdCC, HCC, or EC from January 2015 to April 2023. LEN first and last doses were estimated as a percentage of the standard dose approved for each indication. Differences in the BMI distribution assessed at baseline and end of treatment were assessed with Mann-Whitney test. Differences in intrapatient BMI variation were assessed with Kruskal-Wallis test. DoT and overall survival (OS) were estimated with the Kaplan-Meier method.

Results: Over a period of 8 years and 3 months, n.161 patients were included: n.64 DTC, n.31 AdCC, n.41 HCC, and n.25 EC. Median follow-up (mFUP) was 72.8 months. Overall, median age at diagnosis was 61.8 years, with an ECOG PS 2 in 2%-9% of cases. The most frequently observed AE was fatigue. For the net of different cancer types, baseline BW/BMI, LEN doses, and mFUP, the BMI distribution was lower at last LEN administration compared to baseline (p = 0.045).

Conclusion: Despite the higher prevalence of elderly subjects and ECOG PS 2, our series confirmed the long-term manageability and effectiveness of LEN in the real world. Patients with a baseline low BMI require special attention, as LEN treatment can be implicated in further BW decrease.

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Lenvatinib在晚期甲状腺、唾液腺、子宫内膜和肝细胞癌中的应用:一项关于治疗时间和毒性管理的真实世界研究。
背景:Lenvatinib (LEN)是一种多激酶抑制剂,用于不同的肿瘤:进展或耐放射性碘的晚期分化甲状腺癌(RAIR DTC)、唾液腺腺样囊性癌(AdCC)、肝细胞癌(HCC)和子宫内膜癌(EC)。在现实环境中,有资格接受LEN治疗的患者通常有多种合并症和/或东部肿瘤合作组(ECOG PS)的表现状况受损。目的:本研究旨在调查HCC患者的毒性、治疗持续时间(DoT),并描述现实世界中BW和体重指数(BMI)在患者体内的变化。设计:在三级肿瘤中心进行回顾性观察性研究。方法:我们收集了2015年1月至2023年4月期间连续接受LEN治疗DTC、AdCC、HCC或EC的成年患者的临床特征和ae。LEN首次和末次剂量按每一适应症批准的标准剂量的百分比估计。基线和治疗结束时BMI分布的差异用Mann-Whitney检验评估。采用Kruskal-Wallis检验评估患者体内BMI差异。采用Kaplan-Meier法估计DoT和总生存期(OS)。结果:在8年3个月的时间里,共纳入n161例患者DTC, n.31AdCC, n.41肝癌,n.25电子商务。中位随访(mFUP)为72.8个月。总体而言,诊断时的中位年龄为61.8岁,2%-9%的病例ECOG ps2。最常见的AE是疲劳。对于不同癌症类型、基线BW/BMI、LEN剂量和mFUP,与基线相比,最后一次LEN给药时BMI分布较低(p = 0.045)。结论:尽管老年受试者和ECOG ps2的患病率较高,但我们的系列研究证实了LEN在现实世界中的长期可管理性和有效性。基线BMI较低的患者需要特别注意,因为LEN治疗可能会导致体重进一步下降。
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来源期刊
CiteScore
8.20
自引率
2.00%
发文量
160
审稿时长
15 weeks
期刊介绍: Therapeutic Advances in Medical Oncology is an open access, peer-reviewed journal delivering the highest quality articles, reviews, and scholarly comment on pioneering efforts and innovative studies in the medical treatment of cancer. The journal has a strong clinical and pharmacological focus and is aimed at clinicians and researchers in medical oncology, providing a forum in print and online for publishing the highest quality articles in this area. This journal is a member of the Committee on Publication Ethics (COPE).
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