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仑伐替尼在真实临床实践中治疗放射性碘难治性甲状腺癌的应用

Lenvatinib for the Treatment of Radioiodine-Refractory Thyroid Cancer in Real-Life Practice.

作者信息

Berdelou Amandine, Borget Isabelle, Godbert Yann, Nguyen Thierry, Garcia Marie-Eve, Chougnet Cécile N, Ferru Aurélie, Buffet Camille, Chabre Olivier, Huillard Olivier, Leboulleux Sophie, Schlumberger Martin

机构信息

Department of Nuclear Medicine and Endocrine Oncology, Gustave Roussy and Université Paris-Saclay, Villejuif, France.

Department of Nuclear Medicine and Endocrine Oncology, Institut Curie, Saint-Cloud, France.

出版信息

Thyroid. 2018 Jan;28(1):72-78. doi: 10.1089/thy.2017.0205. Epub 2017 Nov 27.

Abstract

In the Study of (E7080) Lenvatinib in Differentiated Cancer of the Thyroid (SELECT) phase 3 trial on advanced radioactive iodine-refractory differentiated thyroid cancer (rDTC), lenvatinib improved median progression-free survival over placebo by almost 15 months and induces an objective response rate of 64.8%, but adverse events occurred in almost all patients. The present study evaluates the efficacy and toxicity of lenvatinib treatment in real-life practice. Clinical charts of 88 consecutive patients treated with lenvatinib from July 2015 to June 2016 in 27 French centers were retrospectively reviewed. Patients treated for other thyroid cancer types ( = 11) or previously treated with lenvatinib within a trial ( = 2) were excluded and the remaining 75 rDTC patients formed the basis of this report. 75 rDTC patients were analyzed (33 females, median age 65 years [range, 35-88 years]), 12 had an Eastern Cooperative Oncology Group performance status ≥2; 24 cases received lenvatinib as first line systemic treatment; 47 (63%) patients had documented progressive disease prior to treatment initiation. Distant metastases were located in lungs, bones, and lymph nodes (89%, 60%, and 69%, respectively). The initial treatment dose was 24 mg in 54 patients and was lower in the other 21 patients. The median follow-up was 7 months, with a median duration of treatment of 6 months [0.3-15]. Median progression-free survival was 10 months. Among the 65 patients with evaluation of tumor response during treatment, best tumor response was a partial response in 23 patients (31%) and stable disease in 38 (51%). Eleven patients (14.7%) discontinued lenvatinib because of disease progression. Forty-four (59%) and 23 (31%) patients had dose reductions or an interruption of lenvatinib for adverse events (AEs). The most frequent AEs related to treatment were fatigue, hypertension, weight loss, diarrhea, and anorexia. Eleven deaths occurred during the study (one considered to be drug related). Pneumothorax occurred in 2 patients with lung metastases. Real-life patients with rDTC can benefit from lenvatinib treatment. AEs are frequent and should be closely monitored.

摘要

在一项关于(E7080)乐伐替尼治疗分化型甲状腺癌(SELECT)的3期试验中,针对晚期放射性碘难治性分化型甲状腺癌(rDTC),乐伐替尼较安慰剂显著改善了无进展生存期的中位数,延长近15个月,并诱导产生了64.8%的客观缓解率,但几乎所有患者均出现了不良事件。本研究评估了乐伐替尼在实际临床应用中的疗效和毒性。回顾性分析了2015年7月至2016年6月期间在法国27个中心接受乐伐替尼治疗的88例连续患者的临床病历。排除治疗其他类型甲状腺癌的患者(n = 11)或在试验中曾接受过乐伐替尼治疗的患者(n = 2),其余75例rDTC患者构成了本报告的基础。分析了75例rDTC患者(33例女性,年龄中位数65岁[范围35 - 88岁]),12例东部肿瘤协作组体能状态评分为≥2;24例患者接受乐伐替尼作为一线全身治疗;47例(63%)患者在开始治疗前有记录的疾病进展。远处转移分别位于肺、骨和淋巴结(分别为89%、60%和69%)。54例患者的初始治疗剂量为24mg,其他21例患者剂量较低。中位随访时间为7个月,中位治疗持续时间为6个月[0.3 - 15]。无进展生存期的中位数为10个月。在65例治疗期间评估了肿瘤反应的患者中,最佳肿瘤反应为部分缓解的有23例(31%),疾病稳定的有38例(51%)。11例患者(14.7%)因疾病进展停用乐伐替尼。44例(59%)和23例(31%)患者因不良事件(AE)减少了乐伐替尼剂量或中断用药。与治疗相关的最常见AE为疲劳、高血压、体重减轻、腹泻和厌食。研究期间发生了11例死亡(1例被认为与药物相关)。2例肺转移患者发生了气胸。rDTC的实际临床患者可从乐伐替尼治疗中获益。AE很常见,应密切监测。

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