Effect of Everolimus on Prognosis of Neurofibromatosis Type 1 Lesions: A Systematic Review and Meta Analysis.

Everolimus Lesion size NF-1 Neurofibromatosis Type-1 mTOR inhibitor

Journal

Clinical therapeutics
ISSN: 1879-114X
Titre abrégé: Clin Ther
Pays: United States
ID NLM: 7706726

Informations de publication

Date de publication:
06 Sep 2024
Historique:
received: 04 02 2024
accepted: 12 08 2024
medline: 8 9 2024
pubmed: 8 9 2024
entrez: 7 9 2024
Statut: aheadofprint

Résumé

This study addresses the effectiveness of oral everolimus in treating various malignancies associated with Neurofibromatosis Type 1 (NF1). The purpose is to determine whether everolimus reduces lesion size in NF1 patients, considering the controversial findings from previous clinical trials. The scientific hypotheses and questions involve evaluating the impact of everolimus on NF1-associated lesions and understanding the variability in treatment outcomes. A systematic review and meta-analysis were conducted following PRISMA and Cochrane Collaboration guidelines. The study included four-phase II, single-arm, nonrandomized trials investigating the effect of oral everolimus on NF1-associated lesion size. The search covered multiple databases, and data extraction involved evaluating studies for inclusion criteria and assessing quality using the Cochrane Collaboration's Risk of Bias in Nonrandomized Studies tool. Statistical analysis utilized Open Meta(Analyst). The search yielded 388 studies, with 10 selected for full-text review and four included in the final analysis. The quality of the studies ranged from low to moderate. The meta-analysis indicated no observed heterogeneity (I^2 = 0%), and the overall estimate suggested no significant reduction in NF1-associated lesion size with everolimus (P = 0.069). The findings reveal a varied and inconsistent picture of everolimus efficacy in NF1 treatment. The study highlights the need for personalized approaches, considering individual genetic and clinical differences. The limitations, including small sample sizes and nonrandomized trials, call for larger, more standardized research efforts. The study emphasizes ongoing trials and the importance of future research in understanding predictors of everolimus response and optimizing treatment strategies for NF1 patients. While everolimus shows promise in reducing lesion size in a subset of NF1 patients, the study cannot draw conclusive results due to limitations in the included studies. Ongoing, adequately powered trials are crucial for advancing the evidence base and informing the potential role of everolimus in NF1 treatment. There was no funding for this review and no conflicts of interest.

Identifiants

pubmed: 39244488
pii: S0149-2918(24)00220-0
doi: 10.1016/j.clinthera.2024.08.009
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2024 Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Ismail A Ibrahim (IA)

Faculty of Health Sciences, Fenerbahce University, Istanbul, Turkey.

Rem Ehab Abdelkader (RE)

Mansoura Manchester Program for Medical Education, Mansoura University, Mansoura, Egypt.

Ahmed Hosney Nada (AH)

Faculty of Medicine, Benha University, Benha, Egypt.

Siham Younes (S)

Faculty of Medicine, University of Jordan, Amman, Jordan.

George Hanen (G)

Faculty of Medicine, Minia University, Minia, Egypt.

Ghena Shahwan (G)

Faculty of Medicine, The Hashemite University, Amman, Jordan.

Mohammad Hamad (M)

Faculty of Medicine, University of Jordan, Amman, Jordan.

Mostafa Meshref (M)

Department of Neurology, Faculty of Medicine, Al-Azhar university, Cairo, Egypt.

Abdulqadir J Nashwan (AJ)

Hamad Medical Corporation, Doha, Qatar. Electronic address: anashwan@hamad.qa.

Classifications MeSH