The treatment of aggressive prolactinomas with everolimus.


Journal

Pituitary
ISSN: 1573-7403
Titre abrégé: Pituitary
Pays: United States
ID NLM: 9814578

Informations de publication

Date de publication:
Aug 2023
Historique:
accepted: 03 07 2023
medline: 3 8 2023
pubmed: 10 7 2023
entrez: 10 7 2023
Statut: ppublish

Résumé

Aggressive prolactinomas are life-limiting tumors without a standard of care treatment option after the oral alkylator, temozolomide, fails to provide tumor control. We reviewed an institutional database of pituitary tumors for patients with aggressive prolactinomas who progressed following treatment with a dopamine receptor agonist, radiotherapy and temozolomide. Within this cohort, we identified four patients who were treated with everolimus and we report their response to this therapy. Treatment response was determined by a neuroradiologist, who manually performed volumetric assessment and determined treatment response by Response Assessments in Neuro-Oncology (RANO) criteria. Three of four patients who were treated with everolimus had a biochemical response to therapy and all patients derived a clinically meaningful benefit based upon suppression of tumor growth. While the best overall response as assessed by RANO criteria was stable disease for the four patients, a minor regression in tumor size was appreciated in two of the four patients. Everolimus is an active agent in the treatment of prolactinomas that warrants further investigation.

Identifiants

pubmed: 37428396
doi: 10.1007/s11102-023-01340-5
pii: 10.1007/s11102-023-01340-5
doi:

Substances chimiques

Everolimus 9HW64Q8G6G
Temozolomide YF1K15M17Y
Dopamine Agonists 0

Types de publication

Review Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

474-481

Subventions

Organisme : NIH HHS
ID : P30 CA008748
Pays : United States
Organisme : NIH HHS
ID : P30 CA008748
Pays : United States

Informations de copyright

© 2023. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.

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Auteurs

Andrew L Lin (AL)

Department of Neurosurgery, Memorial Sloan Kettering Cancer Center, New York, NY, USA. lina1@mskcc.org.
Department of Neurology, Memorial Sloan Kettering Cancer Center, 1275 York Avenue, New York, NY, 10065, USA. lina1@mskcc.org.
Multidisciplinary Pituitary and Skull Base Tumor Center, Memorial Sloan Kettering Cancer Center, New York, NY, USA. lina1@mskcc.org.
Department of Neurology, Weill Cornell Medical College, New York, NY, USA. lina1@mskcc.org.

Eliza B Geer (EB)

Department of Neurosurgery, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Multidisciplinary Pituitary and Skull Base Tumor Center, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

Nupur Lala (N)

Department of Neurology, Memorial Sloan Kettering Cancer Center, 1275 York Avenue, New York, NY, 10065, USA.

Gabrielle Page-Wilson (G)

Department of Medicine, Columbia University Medical Center, New York, NY, USA.

Rajiv Magge (R)

Department of Neurology, Weill Cornell Medical College, New York, NY, USA.

Robert J Young (RJ)

Department of Radiology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

Viviane Tabar (V)

Department of Neurosurgery, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Multidisciplinary Pituitary and Skull Base Tumor Center, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

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