Cancer Genetics Branch (S.A.W.), National Cancer Institute, Bethesda, Maryland 20892; and Dipartimento di Medicina Molecolare e Biotecnologie Mediche (M.S.), Universita' di Napoli "Federico II," 80131 Napoli, Italy.
J Clin Endocrinol Metab. 2014 May;99(5):1543-55. doi: 10.1210/jc.2013-2622. Epub 2014 Jan 13.
Thyroid cancer is usually cured by timely thyroidectomy; however, the treatment of patients with advanced disease is challenging because their tumors are mostly unresponsive to conventional therapies. Recently, the malignancy has attracted much interest for two reasons: the dramatic increase in its incidence over the last three decades, and the discovery of the genetic mutations or chromosomal rearrangements causing most histological types of thyroid cancer.
This update reviews the molecular genetics of thyroid cancer and the clinical trials evaluating kinase inhibitors (KIs) in patients with locally advanced or metastatic disease. The update also reviews studies in other malignancies, which have identified mechanisms of efficacy, and also resistance, to specific KIs. This information has been critical both to the development of effective second-generation drugs and to the design of combinatorial therapeutic regimens. Finally, the update addresses the major challenges facing clinicians who seek to develop more effective therapy for patients with thyroid cancer.
PubMed was searched from January 2000 to November 2013 using the following terms: thyroid cancer, treatment of thyroid cancer, clinical trials in thyroid cancer, small molecule therapeutics, kinase inhibitors, and next generation sequencing.
A new era in cancer therapy has emerged based on the introduction of KIs for the treatment of patients with liquid and solid organ malignancies. Patients with thyroid cancer have benefited from this advance and will continue to do so with the development of drugs having greater specificity and with the implementation of clinical trials of combined therapeutics to overcome drug resistance.
甲状腺癌通常通过及时的甲状腺切除术治愈;然而,晚期疾病患者的治疗具有挑战性,因为他们的肿瘤对常规疗法大多没有反应。最近,由于两个原因,这种恶性肿瘤引起了广泛关注:过去三十年中发病率的急剧上升,以及发现导致大多数甲状腺癌组织学类型的基因突变或染色体重排。
本综述回顾了甲状腺癌的分子遗传学,以及评估局部晚期或转移性疾病患者中激酶抑制剂(KIs)的临床试验。本综述还回顾了其他恶性肿瘤的研究,这些研究确定了特定 KIs 的疗效和耐药机制。这些信息对于开发有效的第二代药物和设计组合治疗方案都至关重要。最后,本综述还探讨了寻求为甲状腺癌患者开发更有效疗法的临床医生所面临的主要挑战。
从 2000 年 1 月至 2013 年 11 月,使用以下术语在 PubMed 上进行了搜索:甲状腺癌、甲状腺癌治疗、甲状腺癌临床试验、小分子治疗、激酶抑制剂和下一代测序。
基于 KIs 治疗液体和实体器官恶性肿瘤患者的应用,癌症治疗已经进入了一个新时代。甲状腺癌患者已经从这一进展中受益,并且随着开发具有更高特异性的药物和实施联合治疗临床试验以克服耐药性,他们将继续受益。