Abstract
Introduction: Thymic tumors including thymomas, thymic carcinomas, and thymic carcinoid tumors are rare tumors with an incidence of 0.13/100,000. Materials and methods: A literature search was performed to identify recent findings on epidemiology, classification, and various therapeutic approaches. Results: These tumors with a wide spectrum of histologic and biologic features may be clinically unapparent for a long time or show a very aggressive behavior with local invasion and distant metastases. Surgical resection is the mainstay in stage I and II thymomas, whereas in stage III thymomas and in thymomas with pleural dissemination surgery in context of a multimodal treatment should be discussed. Thymic tumors are chemoreactive. Targeted therapies show poor results and should only be considered in the palliative situation after failure of chemotherapy. Conclusion: The new TNM (T: tumor, N: node, M: metastasis) classification of thymic tumors will help to identify the best treatment options.
Translated title of the contribution | Thymus cancers |
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Original language | German |
Pages (from-to) | 859-874 |
Number of pages | 16 |
Journal | Onkologe |
Volume | 21 |
Issue number | 9 |
DOIs | |
State | Published - 1 Oct 2015 |
Externally published | Yes |