Neuroendocrine Tumors, Version 1.2015 JOURNAL OF THE NATIONAL COMPREHENSIVE CANCER NETWORK Kulke, M. H., Shah, M. H., Benson, A. B., Bergsland, E., Berlin, J. D., Blaszkowsky, L. S., Emerson, L., Engstrom, P. F., Fanta, P., Giordano, T., Goldner, W. S., Halfdanarson, T. R., Heslin, M. J., Kandeel, F., Kunz, P. L., Kuvshinoff, B. W., Lieu, C., Moley, J. F., Munene, G., Pillarisetty, V. G., Saltz, L., Sosa, J. A., Strosberg, J. R., Vauthey, J., Wolfgang, C., Yao, J. C., Burns, J., Freedman-Cass, D. 2015; 13 (1): 78-108


Neuroendocrine tumors (NETs) comprise a broad family of tumors that may or may not be associated with symptoms attributable to hormonal hypersecretion. The NCCN Clinical Practice Guidelines in Oncology for Neuroendocrine Tumors discuss the diagnosis and management of both sporadic and hereditary NETs. This selection from the guidelines focuses on sporadic NETs of the pancreas, gastrointestinal tract, lung, and thymus.

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