Emerging and Novel Treatments for Pituitary Tumors

A subset of pituitary neuroendocrine tumors (PitNETs) have an aggressive behavior, showing resistance to treatment and/or multiple recurrences in spite of the optimal use of standard therapies (surgery, conventional medical treatments, and radiotherapy). To date, for aggressive PitNETs, temozolomide...

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Main Authors: Mirela Diana Ilie, Hélène Lasolle, Gérald Raverot
Format: Article
Language:English
Published: MDPI AG 2019-07-01
Series:Journal of Clinical Medicine
Subjects:
Online Access:https://www.mdpi.com/2077-0383/8/8/1107
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spelling doaj-fe42316952c7427ba88935614987c6702020-11-24T21:34:31ZengMDPI AGJournal of Clinical Medicine2077-03832019-07-0188110710.3390/jcm8081107jcm8081107Emerging and Novel Treatments for Pituitary TumorsMirela Diana Ilie0Hélène Lasolle1Gérald Raverot2INSERM U1052, CNRS UMR5286, Cancer Research Center of Lyon, 28 Laennec Street, 69008 Lyon, FranceINSERM U1052, CNRS UMR5286, Cancer Research Center of Lyon, 28 Laennec Street, 69008 Lyon, FranceINSERM U1052, CNRS UMR5286, Cancer Research Center of Lyon, 28 Laennec Street, 69008 Lyon, FranceA subset of pituitary neuroendocrine tumors (PitNETs) have an aggressive behavior, showing resistance to treatment and/or multiple recurrences in spite of the optimal use of standard therapies (surgery, conventional medical treatments, and radiotherapy). To date, for aggressive PitNETs, temozolomide (TMZ) has been the most used therapeutic option, and has resulted in an improvement in the five-year survival rate in responders. However, given the fact that roughly only one third of patients showed a partial or complete radiological response on the first course of TMZ, and even fewer patients responded to a second course of TMZ, other treatment options are urgently needed. Emerging therapies consist predominantly of peptide receptor radionuclide therapy (20 cases), vascular endothelial growth factor receptor-targeted therapy (12 cases), tyrosine kinase inhibitors (10 cases), mammalian target of rapamycin (mTOR) inhibitors (six cases), and more recently, immune checkpoint inhibitors (one case). Here, we present the available clinical cases published in the literature for each of these treatments. The therapies that currently show the most promise (based on the achievement of partial radiological response in a certain number of cases) are immune checkpoint inhibitors, peptide receptor radionuclide therapy, and vascular endothelial growth factor receptor-targeted therapy. In the future, further improvement of these therapies and the development of other novel therapies, their use in personalized medicine, and a better understanding of combination therapies, will hopefully result in better outcomes for patients bearing aggressive PitNETs.https://www.mdpi.com/2077-0383/8/8/1107pituitary neuroendocrine tumors (PitNETs)pituitary adenomaaggressive pituitary tumorstreatmenttemozolomidepeptide receptor radionuclide therapybevacizumabtyrosine kinase inhibitorseverolimusimmunotherapy
collection DOAJ
language English
format Article
sources DOAJ
author Mirela Diana Ilie
Hélène Lasolle
Gérald Raverot
spellingShingle Mirela Diana Ilie
Hélène Lasolle
Gérald Raverot
Emerging and Novel Treatments for Pituitary Tumors
Journal of Clinical Medicine
pituitary neuroendocrine tumors (PitNETs)
pituitary adenoma
aggressive pituitary tumors
treatment
temozolomide
peptide receptor radionuclide therapy
bevacizumab
tyrosine kinase inhibitors
everolimus
immunotherapy
author_facet Mirela Diana Ilie
Hélène Lasolle
Gérald Raverot
author_sort Mirela Diana Ilie
title Emerging and Novel Treatments for Pituitary Tumors
title_short Emerging and Novel Treatments for Pituitary Tumors
title_full Emerging and Novel Treatments for Pituitary Tumors
title_fullStr Emerging and Novel Treatments for Pituitary Tumors
title_full_unstemmed Emerging and Novel Treatments for Pituitary Tumors
title_sort emerging and novel treatments for pituitary tumors
publisher MDPI AG
series Journal of Clinical Medicine
issn 2077-0383
publishDate 2019-07-01
description A subset of pituitary neuroendocrine tumors (PitNETs) have an aggressive behavior, showing resistance to treatment and/or multiple recurrences in spite of the optimal use of standard therapies (surgery, conventional medical treatments, and radiotherapy). To date, for aggressive PitNETs, temozolomide (TMZ) has been the most used therapeutic option, and has resulted in an improvement in the five-year survival rate in responders. However, given the fact that roughly only one third of patients showed a partial or complete radiological response on the first course of TMZ, and even fewer patients responded to a second course of TMZ, other treatment options are urgently needed. Emerging therapies consist predominantly of peptide receptor radionuclide therapy (20 cases), vascular endothelial growth factor receptor-targeted therapy (12 cases), tyrosine kinase inhibitors (10 cases), mammalian target of rapamycin (mTOR) inhibitors (six cases), and more recently, immune checkpoint inhibitors (one case). Here, we present the available clinical cases published in the literature for each of these treatments. The therapies that currently show the most promise (based on the achievement of partial radiological response in a certain number of cases) are immune checkpoint inhibitors, peptide receptor radionuclide therapy, and vascular endothelial growth factor receptor-targeted therapy. In the future, further improvement of these therapies and the development of other novel therapies, their use in personalized medicine, and a better understanding of combination therapies, will hopefully result in better outcomes for patients bearing aggressive PitNETs.
topic pituitary neuroendocrine tumors (PitNETs)
pituitary adenoma
aggressive pituitary tumors
treatment
temozolomide
peptide receptor radionuclide therapy
bevacizumab
tyrosine kinase inhibitors
everolimus
immunotherapy
url https://www.mdpi.com/2077-0383/8/8/1107
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