| Literature DB >> 28550464 |
M Albertelli1, E Nazzari1, S Sciallero2, F Grillo3, S Morbelli4, F De Cian5, G Cittadini6, E Ambrosetti1, A Ciarmiello7, D Ferone8,9.
Abstract
Octreotide and lanreotide, the first-generation somatostatin analogs, successfully control hormone hyperproduction, and related syndromes, in patients with acromegaly and neuroendocrine tumors. However, their anti-tumor effect, rather evident in large number of pituitary adenomas in acromegalic patients, has been hypothesized for a long time in patients with neuroendocrine tumors as well, although a significant tumor shrinkage has rarely been observed. However, the recent publication of the CLARINET study has strengthened the evidence, already emerged with the PROMID trial, that the long-term treatment with the first-generation long-acting somatostatin analogs may exert an anti-tumor activity on G1 and G2 enteropancreatic neuroendocrine tumors, as well. After the publication, majority of international guidelines have updated their algorithms in line with these results and this class of drugs obtained the indication as anti-tumor agents in the majority of patients with neuroendocrine tumors.Entities:
Keywords: Anti-tumor effect; Clinical trial; Lanreotide; Neuroendocrine tumors; Octreotide; Somatostatin analogs
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Year: 2017 PMID: 28550464 DOI: 10.1007/s40618-017-0692-0
Source DB: PubMed Journal: J Endocrinol Invest ISSN: 0391-4097 Impact factor: 4.256