Beneficial Effects of the mTOR Inhibitor Everolimus in Patients with Advanced Medullary Thyroid Carcinoma: Subgroup Results of a Phase II Trial

被引:36
|
作者
Schneider, T. C. [1 ,2 ]
de Wit, D. [3 ]
Links, T. P. [4 ]
van Erp, N. P. [5 ]
van der Hoeven, J. J. M. [1 ]
Gelderblom, H. [1 ]
van Wezel, T. [2 ]
van Eijk, R. [2 ]
Morreau, H. [2 ]
Guchelaar, H. J. [3 ]
Kapiteijn, E. [1 ]
机构
[1] Leiden Univ, Med Ctr, Dept Med Oncol, NL-2333 ZA Leiden, Netherlands
[2] Leiden Univ, Med Ctr, Dept Pathol, NL-2333 ZA Leiden, Netherlands
[3] Leiden Univ, Med Ctr, Dept Clin Pharm & Toxicol, NL-2333 ZA Leiden, Netherlands
[4] Univ Groningen, Univ Med Ctr Groningen, Dept Endocrinol, NL-9700 RB Groningen, Netherlands
[5] Radboud Univ Nijmegen, Med Ctr, Dept Clin Pharm, NL-6525 GA Nijmegen, Netherlands
关键词
ORAL MAMMALIAN TARGET; RAD001; EVEROLIMUS; CANCER; CABOZANTINIB; ACTIVATION; OCTREOTIDE; MUTATIONS; PATHWAY; TUMORS; EGFR;
D O I
10.1155/2015/348124
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
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.
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页数:8
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