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Long-Term Clinical Outcomes of Patients with Differentiated Thyroid Cancer Treated with Lenvatinib: Results from Real-World Practice in Japan

伦瓦提尼 医学 甲状腺癌 肿瘤科 期限(时间) 内科学 临床实习 真实世界数据 重症监护医学 癌症 家庭医学 计算机科学 数据科学 量子力学 物理
作者
Ryutaro Onaga,Tomohiro Enokida,Nobukazu Tanaka,Yuta Hoshi,Takuma Kishida,Ryo Kuboki,Masanobu Sato,Naohiro Takeshita,Hideki Tanaka,Takao Fujisawa,Susumu Okano,Hiroshi Nishino,Makoto Ito,Makoto Tahara
出处
期刊:Thyroid [Mary Ann Liebert, Inc.]
卷期号:35 (7): 781-788
标识
DOI:10.1089/thy.2025.0040
摘要

Background: Although accumulated experience with lenvatinib in patients with differentiated thyroid cancer (DTC) and progressive radioactive iodine (RAI)-refractory disease has been used to improve management strategies for this disease, findings regarding the actual clinical picture and long-term observation data are insufficient. Methods: We conducted a retrospective cohort study of patients with DTC who received lenvatinib treatment from 2011 to 2022 at the National Cancer Center Hospital East, Japan. The patients were treated under the following treatment and management policies (1) starting dose at 24 mg/day, (2) schedule modification according to individual adverse events status (planned drug holidays), (3) dose escalation of lenvatinib, and (4) local therapy at disease progression, if applicable. This is a retrospective cohort study, although some patients were enrolled in a prospective clinical trial (NCT01321554 and UMIN000022243). Results: Of 91 patients, 59 (64.8%) had papillary carcinoma and 22 (24.2%) had follicular carcinoma. Best overall response in all patients was 60.4% (partial response in 55 and complete response in 0). With a median observation period of 2.9 years (range, 0.1-12.4; interquartile range, 1.7-4.6) under supportive management, including the planned drug holidays (n = 72, 79.1%), dose escalation of lenvatinib at systemic disease progression (n = 21, 23.1%), and local therapy for oligoprogressive disease (n = 11, 12.1%), median progression-free survival and overall survival were 2.4 years (95% confidence interval [CI] 1.9-3.3) and 5.1 years (95% CI 3.3-6.7), respectively. At the time of data cutoff, 19.8% had discontinued lenvatinib treatment due to adverse events, although no adverse event was grade 5. Conclusions: In patients with RAI-refractory DTC treated with lenvatinib, careful treatment optimization and management of adverse events contribute to a favorable, durable prognosis.
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