BRAF and MEK inhibitor targeted therapy in papillary craniopharyngiomas: a cohort study.
Humans
Female
Male
Middle Aged
Proto-Oncogene Proteins B-raf
/ antagonists & inhibitors
Adult
Retrospective Studies
Craniopharyngioma
/ drug therapy
Pyridones
/ therapeutic use
Aged
Pituitary Neoplasms
/ drug therapy
Pyrimidinones
/ therapeutic use
Oximes
/ therapeutic use
Cohort Studies
Protein Kinase Inhibitors
/ therapeutic use
Molecular Targeted Therapy
/ methods
Imidazoles
/ therapeutic use
Treatment Outcome
Antineoplastic Combined Chemotherapy Protocols
/ therapeutic use
BRAF and MEK inhibitors
medical treatment
neoadjuvant
papillary craniopharyngiomas
targeted therapy
Journal
European journal of endocrinology
ISSN: 1479-683X
Titre abrégé: Eur J Endocrinol
Pays: England
ID NLM: 9423848
Informations de publication
Date de publication:
05 Aug 2024
05 Aug 2024
Historique:
received:
17
04
2024
revised:
05
06
2024
medline:
19
8
2024
pubmed:
19
8
2024
entrez:
19
8
2024
Statut:
ppublish
Résumé
Targeted therapy (TT) with BRAF/MEK inhibitors has emerged as a potential treatment in papillary craniopharyngiomas (PCPs). However, standardized data on large cohorts are lacking. Our study aimed to assess real-life efficacy and safety of BRAF/MEK inhibition in patients with PCPs. Retrospective French multicenter study involving BRAF V600E-mutated PCP patients, treated with BRAF/MEK inhibitor combination dabrafenib and trametinib, from April 2019 to July 2023. Objective response and clinical and safety outcomes were assessed after 3 months and at the last available follow-up during TT. Sixteen patients (8 females, mean age 50.5 ± 15.75 years), receiving either neoadjuvant therapy (NEO) for non-resectable tumors (n = 6), post-surgical adjuvant therapy (ADJ; n = 8), or palliative therapy (PAL) following failure of multimodal treatment (n = 2), were included.At the last follow-up (mean 7.6 ± 5.3 months), 12 patients showed subtotal response, 3 exhibited partial response, and 1 maintained stable disease. Mean volume reduction was 88.9 ± 4.4%, 73.3 ± 23.4%, and 91.8 ± 4.3% in the NEO, ADJ, and PAL groups, respectively.Targeted therapy resolved headaches in 5/5 patients and visual impairment in 6/9; 2/3 patients had improved neurological symptoms, 1/4 presented weight loss, and 2/14 recovered endocrine function.Targeted therapy was well-tolerated in 62.5% of cases; adverse events led to treatment discontinuation in 5 patients and definitive discontinuation in 3 cases. In this study, 94% of patients showed partial response or better to TT. Adverse events were acceptable. Further research is needed to establish standardized protocols; however, these results advocate for a NEO approach in invasive PCPs.
Identifiants
pubmed: 39158090
pii: 7735740
doi: 10.1093/ejendo/lvae091
doi:
Substances chimiques
Proto-Oncogene Proteins B-raf
EC 2.7.11.1
Pyridones
0
trametinib
33E86K87QN
BRAF protein, human
EC 2.7.11.1
Pyrimidinones
0
dabrafenib
QGP4HA4G1B
Oximes
0
Protein Kinase Inhibitors
0
Imidazoles
0
Types de publication
Journal Article
Multicenter Study
Langues
eng
Sous-ensembles de citation
IM
Pagination
251-261Informations de copyright
© The Author(s) 2024. Published by Oxford University Press on behalf of European Society of Endocrinology. All rights reserved. For commercial re-use, please contact reprints@oup.com for reprints and translation rights for reprints. All other permissions can be obtained through our RightsLink service via the Permissions link on the article page on our site—for further information please contact journals.permissions@oup.com.
Déclaration de conflit d'intérêts
Conflict of interest: The authors have no relevant financial or nonfinancial interests to disclose. Co-author G.R. is on the editorial board of EJE. He was not involved in the review or editorial process for this paper, on which they are listed as authors.