Gómez Karen, Varghese Jeena, Jiménez Camilo
Department of Endocrinology, Hospital San Juan de Dios, Avenida 14, Calles 6 Y 7 Paseo Colon, 1475-1000 San José, Costa Rica.
J Thyroid Res. 2011;2011:815826. doi: 10.4061/2011/815826. Epub 2011 May 16.
Research on medullary thyroid carcinoma (MTC) over the last 55 years has led to a good understanding of the genetic defects and altered molecular pathways associated with its development. Currently, with the use of genetic testing, patients at high risk for MTC can be identified before the disease develops and offered prophylactic treatment. In cases of localized neck disease, surgery can be curative. However, once MTC has spread beyond the neck, systemic therapy may be necessary. Conventional chemotherapy has been shown to be ineffective; however, multikinase inhibitors have shown promise in stabilizing disease, and this year will probably see the approval of a drug (Vandetanib) for advanced unresectable or metastatic disease, which represents a new chapter in the history of MTC. In this paper, we explore newly understood molecular pathways and the most promising emerging therapies that may change the management of MTC.
过去55年中对甲状腺髓样癌(MTC)的研究,使人们对与其发生相关的基因缺陷和分子途径改变有了很好的了解。目前,通过基因检测,可以在疾病发生前识别出MTC高危患者,并为其提供预防性治疗。对于局限性颈部疾病,手术可以治愈。然而,一旦MTC扩散到颈部以外,可能需要进行全身治疗。传统化疗已被证明无效;然而,多激酶抑制剂已显示出稳定病情的前景,今年可能会批准一种用于晚期不可切除或转移性疾病的药物(凡德他尼),这代表了MTC治疗史上的新篇章。在本文中,我们探讨了新认识的分子途径以及可能改变MTC治疗方式的最有前景的新兴疗法。