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甲状腺癌中生物标志物驱动的靶向治疗进展

Advances in Biomarker-Driven Targeted Therapies in Thyroid Cancer.

作者信息

Mishra Prachi, Laha Dipranjan, Grant Robert, Nilubol Naris

机构信息

Surgical Oncology Program, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, USA.

出版信息

Cancers (Basel). 2021 Dec 9;13(24):6194. doi: 10.3390/cancers13246194.

Abstract

Thyroid cancer is the most common type of endocrine malignancy comprising 2-3% of all cancers, with a constant rise in the incidence rate. The standard first-line treatments for thyroid cancer include surgery and radioactive iodine ablation, and a majority of patients show a good response to these therapies. Despite a better response and outcome, approximately twenty percent of patients develop disease recurrence and distant metastasis. With improved knowledge of molecular dysregulation and biological characteristics of thyroid cancer, the development of new treatment strategies comprising novel targets has accelerated. Biomarker-driven targeted therapies have now emerged as a trend for personalized treatments in patients with advanced cancers, and several multiple receptor kinase inhibitors have entered clinical trials (phase I/II/III) to evaluate their safety and efficacy. Most extensively investigated and clinically approved targeted therapies in thyroid cancer include the tyrosine receptor kinase inhibitors that target antiangiogenic markers, BRAF mutation, PI3K/AKT, and MAPK pathway components. In this review, we focus on the current advances in targeted mono- and combination therapies for various types of thyroid cancer.

摘要

甲状腺癌是最常见的内分泌恶性肿瘤,占所有癌症的2%-3%,且发病率持续上升。甲状腺癌的标准一线治疗包括手术和放射性碘消融,大多数患者对这些治疗反应良好。尽管治疗反应和结果较好,但仍有大约20%的患者会出现疾病复发和远处转移。随着对甲状腺癌分子失调和生物学特性的认识不断提高,包含新靶点的新治疗策略的开发加速。生物标志物驱动的靶向治疗现已成为晚期癌症患者个性化治疗的趋势,几种多受体激酶抑制剂已进入临床试验(I/II/III期)以评估其安全性和有效性。在甲状腺癌中研究最广泛且临床批准的靶向治疗包括针对抗血管生成标志物、BRAF突变、PI3K/AKT和MAPK通路成分的酪氨酸受体激酶抑制剂。在本综述中,我们关注各种类型甲状腺癌靶向单一疗法和联合疗法的当前进展。

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