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胸腺瘤和胸腺癌:分子病理学与靶向治疗。

Thymoma and thymic carcinoma: molecular pathology and targeted therapy.

机构信息

Institute of Pathology, University Medical Center Mannheim, University of Heidelberg, Mannheim, Germany.

出版信息

J Thorac Oncol. 2010 Oct;5(10 Suppl 4):S286-90. doi: 10.1097/JTO.0b013e3181f209a8.

Abstract

Thymomas and thymic carcinomas (TC) are rare epithelial tumors of the thymus. Although most thymomas have organotypic features (i.e., resemble the normal thymus), TC are morphologically undistinguishable from carcinomas in other organs. Apart from their different morphology, TC and thymomas differ also in functional terms (TC, in contrast to thymomas, have lost the capacity to promote the maturation of intratumorous lymphocytes), have different genetic features (discussed in this review), a different immunoprofile (most TC overexpress c-KIT, whereas thymomas are consistently negative), and different clinical features (TC, in contrast to thymomas, are not associated with paraneoplastic myasthenia gravis). Thus, although all the data suggest that the biology of thymomas and TC is different, in clinical practice, their therapeutic management up to now is identical. In the age of personalized medicine, the time may have come to think this over. We will briefly review the molecular genetics of malignant thymic tumors, summarize the current status of targeted therapies with an emphasis on the multitargeted kinase inhibitors sunitinib and sorafenib, and try to outline some future directions.

摘要

胸腺瘤和胸腺癌(TC)是胸腺罕见的上皮性肿瘤。虽然大多数胸腺瘤具有器官样特征(即类似于正常胸腺),但 TC 在形态上与其他器官的癌无法区分。除了形态不同外,TC 和胸腺瘤在功能上也不同(TC 与胸腺瘤相反,丧失了促进肿瘤内淋巴细胞成熟的能力),具有不同的遗传特征(本文将讨论)、免疫表型(大多数 TC 过度表达 c-KIT,而胸腺瘤始终为阴性)和不同的临床特征(TC 与胸腺瘤相反,与副肿瘤性重症肌无力无关)。因此,尽管所有数据表明胸腺瘤和 TC 的生物学特性不同,但在临床实践中,它们的治疗管理迄今为止是相同的。在个性化医疗时代,现在可能是重新思考这个问题的时候了。我们将简要回顾恶性胸腺瘤的分子遗传学,总结靶向治疗的现状,重点介绍多靶点激酶抑制剂舒尼替尼和索拉非尼,并尝试概述一些未来的方向。

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