Evolving Approaches to Patients with Advanced Differentiated Thyroid Cancer

被引:89
作者
Haugen, Bryan R. [1 ]
Sherman, Steven I. [2 ]
机构
[1] Univ Colorado, Sch Med, Ctr Canc, Aurora, CO 80045 USA
[2] Univ Texas MD Anderson Canc Ctr, Houston, TX 77030 USA
基金
美国国家卫生研究院;
关键词
MEK INHIBITOR PD0325901; PHASE-II TRIAL; BONE METASTASES; BETA-CATENIN; PHOSPHATIDYLINOSITOL; 3-KINASE/AKT; MESENCHYMAL TRANSITION; BRAF(V600E) INHIBITOR; GENETIC ALTERATIONS; ANTITUMOR-ACTIVITY; RADIOIODINE UPTAKE;
D O I
10.1210/er.2012-1038
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Advanced differentiated thyroid cancer (DTC), defined by clinical characteristics including gross extrathyroidal invasion, distant metastases, radioiodine (RAI) resistance, and avidity for 18-fluorodeoxyglucose (positron emission tomography-positive), is found in approximately 10-20% of patients with DTC. Standard therapy (surgery, RAI, TSH suppression with levothyroxine) is ineffective for many of these patients, as is standard chemotherapy. Our understanding of the molecular mechanisms leading to DTC and the transformation to advanced DTC has rapidly evolved over the past 15-20 years. Newer targeted therapy, specifically inhibitors of intracellular kinase signaling pathways, and cooperative multicenter clinical trials have dramatically changed the therapeutic landscape for patients with advanced DTC. In this review focusing on morbidities, molecules, and medicinals, we present a patient with advanced DTC, explore the genetics and molecular biology of advanced DTC, and review evolving therapies for these patients including multikinase inhibitors, selective kinase inhibitors, and combination therapies.
引用
收藏
页码:439 / 455
页数:17
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