Everolimus in the Treatment of Neuroendocrine Tumors of the Respiratory and Gastroenteropancreatic Systems
Author(s) -
Nicola Flaum,
Juan W. Valle,
Wasat Mansoor,
Mairéad G. McNamara
Publication year - 2016
Publication title -
future oncology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.857
H-Index - 72
eISSN - 1744-8301
pISSN - 1479-6694
DOI - 10.2217/fon.16.23
Subject(s) - everolimus , medicine , neuroendocrine tumors , oncology , clinical trial , diarrhea , adverse effect , rash , incidence (geometry) , discovery and development of mtor inhibitors , intensive care medicine , pi3k/akt/mtor pathway , apoptosis , biochemistry , chemistry , physics , optics
Neuroendocrine tumors (NETs) are a rare diverse group of malignancies occurring most commonly in the gastroenteropancreatic system and the lungs. The incidence of NETs is increasing worldwide; median survival for patients with metastatic NETs is 5-65 months. A growing body of evidence shows survival benefit in patients with advanced NETs (gastroenteropancreatic and lung) treated with mTOR inhibitor everolimus, with improvement in survival being demonstrated in the clinical trial and real-world setting. Everolimus has been shown to have a manageable safety profile, with the most common adverse events being stomatitis, rash, diarrhea, fatigue and infections. Due to the rarity of the condition, there are challenges in conducting clinical trials in these patients. Further research is required to clarify the role of adjuvant therapy, treatment sequencing and the use of multimodality treatments.
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