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分化型甲状腺癌和髓样甲状腺癌化疗的进展

Advances in chemotherapy of differentiated epithelial and medullary thyroid cancers.

作者信息

Sherman Steven I

机构信息

Department of Endocrine Neoplasia and Hormonal Disorders, Division of Internal Medicine, The University of Texas M. D. Anderson Cancer Center, Houston, Texas 77230-1402, USA.

出版信息

J Clin Endocrinol Metab. 2009 May;94(5):1493-9. doi: 10.1210/jc.2008-0923. Epub 2009 Mar 3.

Abstract

CONTEXT

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.

EVIDENCE ACQUISITION

The PubMed and Google Scholar search engines were used to identify publications and peer-reviewed meeting presentations addressing chemotherapy and targeted therapy for differentiated or medullary carcinoma.

EVIDENCE SYNTHESIS

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 seen. 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. Randomized trials for several agents are underway that may lead to eventual drug approval for thyroid cancer.

CONCLUSION

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.

摘要

背景

晚期或转移性甲状腺癌的全身化疗效果有限。对于对传统治疗无反应的分化型或髓样癌患者,需要新的治疗方法来改善疾病预后。

证据获取

使用PubMed和谷歌学术搜索引擎来识别关于分化型或髓样癌化疗和靶向治疗的出版物及同行评审会议报告。

证据综合

多种主要靶向血管生成的新型治疗方法已进入转移性甲状腺癌的临床试验。单药研究报告的部分缓解率高达30%,但更常见的是疾病长期稳定。最成功的药物靶向血管内皮生长因子受体,潜在靶点包括与乳头状和髓样肿瘤发生相关的突变激酶。两种已被批准用于其他恶性肿瘤的药物,索拉非尼和舒尼替尼,已报告有令人鼓舞的初步结果,并且正在有选择地用于不符合临床试验条件的患者。几种药物的随机试验正在进行中,可能最终导致甲状腺癌药物获批。

结论

转移性或晚期甲状腺癌患者的治疗现在强调有很大前景的新型药物的临床试验机会。现在存在酪氨酸激酶抑制剂的替代选择,这些抑制剂耐受性良好,可能值得监管机构批准用于这种疾病。

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