首页> 美国卫生研究院文献>International Journal of Endocrinology >Beneficial Effects of the mTOR Inhibitor Everolimus in Patients with Advanced Medullary Thyroid Carcinoma: Subgroup Results of a Phase II Trial
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Beneficial Effects of the mTOR Inhibitor Everolimus in Patients with Advanced Medullary Thyroid Carcinoma: Subgroup Results of a Phase II Trial

机译:mTOR抑制剂依维莫司对晚期髓样甲状腺癌患者的有益作用:II期试验的亚组结果

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摘要

Objective. Until recently, advanced medullary thyroid cancer (MTC) had few treatment options except surgery. The mTOR inhibitor everolimus has shown encouraging results in neuroendocrine tumors. As part of a prospective phase II study, we analyzed the safety and efficacy of everolimus in advanced MTC. Methods. Seven patients with per RECIST 1.1 documented advanced MTC were included and received everolimus 10 mg daily. The primary objective was determining treatment efficacy. Secondary endpoints included progression-free survival (PFS), overall survival (OS), toxicity, and pharmacokinetics (PK). Results. Median follow-up duration was 28 weeks (17–147). Five patients (71%) showed SD, of which 4 (57%) showed SD >24 weeks. Median PFS and OS were 33 (95%CI: 8–56) and 30 (95%CI: 15–45) weeks, respectively. Toxicity was predominantly grade 1/2 and included mucositis (43%), fatigue (43%), and hypertriglyceridemia (43%). Four MTCs harbored the somatic RET mutation c.2753T>C, p.Met918Thr. The best clinical response was seen in a MEN2A patient. PK characteristics were consistent with phase I data. One patient exhibited extensive toxicity accompanying elevated everolimus plasma concentrations. Conclusions. This study suggests that everolimus exerts clinically relevant antitumor activity in patients with advanced MTC. Given the high level of clinical benefit and the relatively low toxicity profile, further investigation of everolimus in these patients is warranted.
机译:目的。直到最近,晚期甲状腺髓样癌(MTC)除手术外几乎没有其他治疗选择。 mTOR抑制剂依维莫司在神经内分泌肿瘤中显示出令人鼓舞的结果。作为一项前瞻性II期研究的一部分,我们分析了依维莫司在晚期MTC中的安全性和有效性。方法。根据RECIST 1.1记录,有7名晚期MTC患者入选,每天接受依维莫司10 mg。主要目的是确定治疗效果。次要终点包括无进展生存期(PFS),总生存期(OS),毒性和药代动力学(PK)。结果。中位随访时间为28周(17-147)。 5名患者(71%)表现为SD,其中4名(57%)表现为SD> 24周。 PFS和OS的中位数分别为33(95%CI:8-56)和30(95%CI:15-45)周。毒性主要为1/2级,包括粘膜炎(43%),疲劳(43%)和高甘油三酯血症(43%)。四个MTC包含体细胞RET突变c.2753T> C,p.Met918Thr。在MEN2A患者中观察到最佳的临床反应。 PK特征与I期数据一致。一名患者在依维莫司血浆浓度升高时表现出广泛的毒性。结论。这项研究表明依维莫司对晚期MTC患者具有临床相关的抗肿瘤活性。鉴于高水平的临床获益和相对较低的毒性,有必要对这些患者进行依维莫司的进一步研究。

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