Diseases [C] » Neoplasms [C04] » Neoplasms by Histologic Type » Neoplasms, Germ Cell and Embryonal » Neuroectodermal Tumors » Neuroendocrine Tumors » Carcinoid Tumor
Diseases [C] » Neoplasms [C04] » Neoplasms by Histologic Type » Neoplasms, Glandular and Epithelial » Carcinoma » Adenocarcinoma » Carcinoid Tumor
Diseases [C] » Neoplasms [C04] » Neoplasms by Histologic Type » Neoplasms, Nerve Tissue » Neuroectodermal Tumors » Neuroendocrine Tumors » Carcinoid Tumor
Description
A usually small, slow-growing neoplasm composed of islands of rounded, oxyphilic, or spindle-shaped cells of medium size, with moderately small vesicular nuclei, and covered by intact mucosa with a yellow cut surface. The tumor can occur anywhere in the gastrointestinal tract (and in the lungs and other sites); approximately 90% arise in the appendix. It is now established that these tumors are of neuroendocrine origin and derive from a primitive stem cell. (From Stedman, 25th ed & Holland et al., Cancer Medicine, 3d ed, p1182) MeSH
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Subtype Terms (1)
Malignant Carcinoid Syndrome
11 drugs (8 approved, 3 experimental)
Approved Indicated Drugs (1)
Phase 2 Indicated Drugs (30)
Phase 1 Indicated Drugs (4)
Other Experimental Indicated Drugs (1)
Organization Involved with Phase 4 Indications (2)
Organization Involved with Phase 3 Indications (14)
Organization Involved with Phase 2 Indications (49)
Cancer Biotherapy Research Group
Cancer Therapeutics, Incorporated
Groupe Cooperateur Multidisciplinaire en Oncologie (GERCOR)
Hammersmith Medicines Research
Molecular Insight Pharmaceuticals
National Comprehensive Cancer Network
Organization Involved with Phase 1 Indications (12)
Organization Involved with Other Experimental Indications (3)
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UMLS Data
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