lenvatinib对放射性碘难治性分化甲状腺癌患者的疗效和耐受性:俄罗斯联邦一项多中心观察性研究的结果

Q4 Medicine
E. Borodavina, P. Isaev, A. Shurinov, P. Rumyantsev, V. Krylov, K. Petrosyan, A. Kaprin, S. A. Ivanov, S. Podvyaznikov, I. Romanov, A. Mudunov, K. Slashchuk, R. Zhikhorev, M. Volkonsky, R. M. Chagova, I. Suslova, A. I. Khryapa, A. K. Lepshokova, N. L. Fadeeva, A. R. Safarova, L. P. Kaleykina, E. V. Lymar, E. Chernyakova, O. A. Snezhko, A. E. Zinkovskaya, F. F. Mufazalov, E. Kuzmina, Y. Druzhinina, S. Musin, M. R. Mukhitova, A. Khasanova, S. Safina, S. L. Kirienko
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引用次数: 2

摘要

背景。酪氨酸激酶抑制剂在临床实践中的应用改善了放射性碘难治性分化型甲状腺癌(RR-DTC)患者的治疗效果。Lenvatinib被推荐作为这些患者的一线药物。研究目的是分析俄罗斯联邦RR-DTC患者使用lenvatinib的临床经验。材料和方法。研究人员分析了2015年12月至2019年9月期间俄罗斯18个临床站点的数据。77例经组织学证实的DTC患者,证实对放射性碘治疗有耐药性,肿瘤进展(根据实体瘤反应评价标准1.1标准)纳入研究。结果。纳入分析的患者中位无进展生存期(n = 72)为26.1个月。在对治疗有反应的患者中(包括部分和完全缓解的患者),中位无进展生存期达到36.2个月,高于SELECT研究的最新结果(33.1个月)。87%的患者观察到lenvatinib相关不良事件(ae)。18.2%的参与者出现严重不良反应。在6.5%的病例中,ae导致lenvatinib停药;在74%的病例中,ae需要减少剂量。我们的研究结果表明,在俄罗斯联邦的常规临床实践中,lenvatinib对RR-DTC患者的疗效高,耐受性好。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Efficacy and tolerability of lenvatinib in patients with radioiodine-refractory differentiated thyroid cancer: results of a multicenter observational study in the Russian Federation
Background. The implementation of tyrosine kinase inhibitors into clinical practice improved treatment outcomes in patients with radioiodine-refractory differentiated thyroid cancer (RR-DTC). Lenvatinib is recommended as a first-line drug for these patients. The study objective is to analyze clinical experience with lenvatinib in patients with RR-DTC in the Russian Federation. Materials and methods. The data from 18 clinical sites in Russia was analyzed for the period December 2015 and September 2019. Seventyseven patients with histologically verified DTC, proven resistance to radioactive iodine therapy, and tumor progression (according to the Response Evaluation Criteria In Solid Tumors 1.1 criteria) were included in the study. Results.Median progression-free survival in patients included into analysis (n = 72) was 26.1 months. In patients who responded to therapy (including those with partial and complete response), median progression-free survival reached 36.2 months, which is higher than that reported in the updated results of the SELECT study (33.1 months). Lenvatinib-associated adverse events (AEs) were observed in 87 % of patients. Severe AEs were registered in 18.2 % of participants. In 6.5 % of cases, AEs lead to lenvatinib cessation; in 74 % of cases, AEs required dose reduction.Conclusion. Our findings suggest high efficacy and good tolerability of lenvatinib in patients with RR-DTC in routine clinical practice in the Russian Federation.
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来源期刊
Opuholi Golovy i Sei
Opuholi Golovy i Sei Medicine-Otorhinolaryngology
CiteScore
0.40
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0.00%
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43
审稿时长
8 weeks
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