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Treatment of gastroenteropancreatic neuroendocrine tumors

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VIRCHOWS ARCHIV
卷 451, 期 -, 页码 S71-S80

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SPRINGER
DOI: 10.1007/s00428-007-0446-z

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gastroenteropancreatic neuroendocrine tumors; biotherapy; somatostatin analogue; interferon; chemotherapy; streptozotocin; tyrosine kinase inhibitor; anti-angiogenic therapy

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Neuroendocrine tumors are rare; thus, individual experience with the diagnosis and treatment of these tumors is mostly low, except in specialized centers. For histological diagnosis, standards have been described recently. Pathological classification and clinical staging influence diagnostic and therapeutic decisions. This chapter aims at demonstrating the importance of pathological and clinical classification of neuroendocrine tumors on therapeutic decisions, indicating the appropriate therapy for different stages of the disease. Surgical therapy will be discussed shortly, including palliative surgical strategies. However, the focus of the manuscript is medical therapy. Biotherapy, its effects, and remaining uncertainties are presented as well as different chemotherapeutic schemes. Finally, new options of palliative medical therapies like kinase inhibitors and anti-angiogenetic drugs will be discussed.

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