| Literature DB >> 27856921 |
Yvonne Hewett1, Subash Ghimire1, Bilal Farooqi2, Binay K Shah3.
Abstract
Lenvatinib, an oral multikinase inhibitor, was approved by the US Food and Drug Administration in February 2015. In a pivotal phase III study of 392 patients with progressive radioiodine-refractory thyroid cancer, the overall response rate of patients receiving lenvatinib was 64.8%, with complete response in four patients. The median progression-free survival was 18.3 months in the lenvatinib arm versus 3.6 months in patients receiving placebo. Median overall survival was not reached in either arm. Lenvatinib is a promising new treatment for patients with radioiodine (iodine-131)-refractory differentiated thyroid cancer.Entities:
Keywords: Differentiated thyroid cancer; lenvatinib; tyrosine kinase inhibitor
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Year: 2016 PMID: 27856921 DOI: 10.1177/1078155216680119
Source DB: PubMed Journal: J Oncol Pharm Pract ISSN: 1078-1552 Impact factor: 1.809