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Treatment of neuroendocrine tumors with somatostatin analogs
Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Medical Sciences. (Onkologisk endokrinologi)
2006 (English)In: Pituitary, ISSN 1386-341X, E-ISSN 1573-7403, Vol. 9, no 3, 249-256 p.Article, review/survey (Other (popular science, discussion, etc.)) Published
Abstract [en]

Neuroendocrine tumors constitute a group of hormone producing tumors originating from neuroendocrine cells in different organs. Most tumors have a low proliferation index measured by Ki67 and the progression of the tumor is slow. However, many patients suffer from endocrine symptoms induced by the hormones produced and released by the tumor cells. For some patients these symptoms can be life- threatening as in midgut carcinoid patients suffering from carcinoid crises with extensive flushes and hypotension or in patients with severe diarrhea induced by tumors producing vasointestinal polypeptide. In many other patients the hormone-induced symptoms interfere with the ability to carry out ordinary daily activities. The introduction of somatostatin analogs in the treatment of these hormone related symptoms has made it possible to control most of them and has added significantly to the quality of life for this group of patients. Unfortunately, the clinical inhibitory effect on tumor growth has not been very good with only 5-10% of the patients showing an objective response. However, stabilization of tumor growth may be achieved in a significant number of patients. In the future, the hope is that development of new somatostatin analogs with broader receptor-binding profiles will give us new analogs which are more efficient with regard to their antiproliferative effect. This possibility will be studied in future trials.

Place, publisher, year, edition, pages
2006. Vol. 9, no 3, 249-256 p.
National Category
Medical and Health Sciences
URN: urn:nbn:se:uu:diva-21432DOI: 10.1007/s11102-006-0271-4PubMedID: 17001461OAI: oai:DiVA.org:uu-21432DiVA: diva2:49205
Available from: 2006-12-28 Created: 2006-12-28 Last updated: 2010-07-23Bibliographically approved

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Publisher's full textPubMedhttp://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Retrieve&list_uids=17001461&dopt=Citation

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Janson, Eva Tiensuu
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