Clinical Evaluation of Everolimus in the Treatment of Neuroendocrine Tumors of the Lung: Patient Selection and Special Considerations. A Systematic and Critical Review of the Literature.
atypical carcinoid
everolimus
lung NET
mammalian target of rapamycin (mTOR) inhibitor
targeted agents
typical carcinoid
Journal
Lung Cancer (Auckland, N.Z.)
ISSN: 1179-2728
Titre abrégé: Lung Cancer (Auckl)
Pays: New Zealand
ID NLM: 101632521
Informations de publication
Date de publication:
2020
2020
Historique:
received:
15
02
2020
accepted:
12
06
2020
entrez:
6
8
2020
pubmed:
6
8
2020
medline:
6
8
2020
Statut:
epublish
Résumé
Neuroendocrine tumors (NETs) of the lung are well-differentiated neuroendocrine neoplasms (NENs) with a heterogeneous clinical behaviour. Unlike gastroenteropancreatic NENs where therapeutic armamentarium clearly increased over the last decade, everolimus represented the only clinical practical innovation for lung NET patients over the last years. Therefore, for lung NETs, a multidisciplinary discussion within a dedicated team remains critical for an adequate decision-making. Although the main regulatory authorities considered the everolimus-related evidence is enough to approve the drug in advanced lung NETs, several clinical features deserve to be discussed. In this review, we systemically and critically analysed the main clinical studies including patients with advanced lung NETs receiving everolimus. Furthermore, we reported the biological and clinical background of everolimus in lung NET setting. The purpose of this review is to help clinical community to contextualize evidence and experience for a personalised use of this drug in clinical practice in the context of advanced lung NET patients.
Identifiants
pubmed: 32753993
doi: 10.2147/LCTT.S249928
pii: 249928
pmc: PMC7355078
doi:
Types de publication
Journal Article
Review
Langues
eng
Pagination
41-52Informations de copyright
© 2020 Peri and Fazio.
Déclaration de conflit d'intérêts
Dr Nicola Fazio reports personal fees and research funds to the institution from Novartis, AAA and Ipsen, and personal fees from Pfizer. The authors report no other conflicts of interest in this work.
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