Advances in the treatment of thyroid cancer in the era of molecularly targeted therapies

被引:3
作者
Malouf, G. [1 ]
Baudin, E. [2 ]
Soria, J. -C. [1 ]
Schlumberger, M. [2 ]
机构
[1] Inst Gustave Roussy, Dept Med, Fac Med Paris Sud, F-94805 Villejuif, France
[2] Inst Gustave Roussy, Dept Med Nucl & Endocrinol Oncol, Fac Med Paris Sud, F-94805 Villejuif, France
关键词
targeted therapies; angiogenesis inhibitors; thyroid cancers; medullary thyroid cancers; tyrosine kinases inhibitors; molecular biology; RET PROTOONCOGENE MUTATIONS; DOXORUBICIN PLUS CISPLATIN; ENDOTHELIAL GROWTH-FACTOR; PHASE-II TRIAL; PAX8-PPAR-GAMMA REARRANGEMENT; CARCINOEMBRYONIC ANTIGEN; HIGH PREVALENCE; BRAF MUTATIONS; CARCINOMA; PAPILLARY;
D O I
10.1684/bdc.2008.0798
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
During last decade, many progresses have been made in the understanding of thyroid cancer molecular biology. This knowledge led to the development of novel targeted therapy in iodine-resistant patients. However, the management of patients remains complex because of the broad spectrum of clinical presentation of thyroid cancers, differences in their natural histories and the lack of data about randomized trials. Angiogenesis inhibitors (sorafenib, motesanib, axitinib and vandetanib) have shown promising activity in differentiated thyroid cancer. Vandetanib, an inhibitor of RET and VEGFR tyrosine-kinases, is promising in medullary thyroid cancers. Preliminary results of these trials are discussed in this review.
引用
收藏
页码:95 / 101
页数:7
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