Targeted therapies for thyroid tumors

被引:59
作者
Sherman, Steven I. [1 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Endocrine Neoplasia & Hormonal Disorders, Houston, TX 77030 USA
关键词
angiogenesis inhibitors; antineoplastic agents; protein kinase inihibitors; thyroid carcinoma; ENDOTHELIAL GROWTH-FACTOR; TYROSINE KINASE INHIBITOR; PHASE-II TRIAL; MULTIKINASE INHIBITOR; ANTITUMOR-ACTIVITY; CANCER INCIDENCE; BRAF MUTATION; SOLID TUMORS; FACTOR VEGF; MEDULLARY;
D O I
10.1038/modpathol.2010.165
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Systemic chemotherapies for advanced or metastatic thyroid carcinomas have been of only limited effectiveness. For patients with differentiated or medullary carcinomas unresponsive to conventional treatments, novel therapies are needed to improve disease outcomes. Multiple novel therapies primarily targeting angiogenesis have entered clinical trials for metastatic thyroid carcinoma. Partial response rates up to 30% have been reported in single-agent studies, but prolonged disease stabilization is more commonly observed. The most successful agents target the vascular endothelial growth factor receptors, with potential targets including the mutant kinases associated with papillary and medullary oncogenesis. Two drugs approved for other malignancies, sorafenib and sunitinib, have had promising preliminary results reported, and are being used selectively for patients who do not qualify for clinical trials. At least one randomized, placebo-controlled phase Ill trial has been successfully completed, showing improved progression-free survival in patients with advanced or metastatic medullary thyroid carcinoma treated with vandetanib. Randomized trials for other agents are currently underway. Treatment for patients with metastatic or advanced thyroid carcinoma now emphasizes clinical trial opportunities for novel agents with considerable promise. Alternative options now exist for use of tyrosine kinase inhibitors that are well tolerated and may prove worthy of regulatory approval for this disease. Modern Pathology (2011) 24, S44-S52; doi:10.1038/modpathol.2010.165
引用
收藏
页码:S44 / S52
页数:9
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