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

dc.contributor.author Ibrahim, Ismail A.
dc.contributor.author Abdelkader, Rem Ehab
dc.contributor.author Nada, Ahmed Hosney
dc.contributor.author Younes, Siham
dc.contributor.author Hanen, George
dc.contributor.author Shahwan, Ghena
dc.contributor.author Nashwan, Abdulqadir J.
dc.date.accessioned 2025-01-11T13:03:23Z
dc.date.available 2025-01-11T13:03:23Z
dc.date.issued 2024
dc.description Abdelkader, Rem/0009-0000-0900-3978; Hanen, George Magdy Halim/0000-0002-8946-2046; Alhamad, Mohammad/0000-0002-2175-1597; Meshref, Mostafa/0000-0003-0692-6309; Nashwan, Abdulqadir/0000-0003-4845-4119; Ibrahim, Ismail/0000-0002-0805-8181 en_US
dc.description.abstract Purpose: 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. Methods: 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). Findings: 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 (I2 = 0%), and the overall estimate suggested no significant reduction in NF1-associated lesion size with everolimus ( P = 0.069). Implications: 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. Conclusion: 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. Others: There was no funding for this review and no conflicts of interest. en_US
dc.identifier.citation 0
dc.identifier.doi 10.1016/j.clinthera.2024.08.009
dc.identifier.issn 0149-2918
dc.identifier.issn 1879-114X
dc.identifier.scopus 2-s2.0-85203274573
dc.identifier.uri https://doi.org/10.1016/j.clinthera.2024.08.009
dc.identifier.uri https://hdl.handle.net/20.500.14627/267
dc.language.iso en en_US
dc.publisher Elsevier en_US
dc.rights info:eu-repo/semantics/closedAccess en_US
dc.subject Everolimus en_US
dc.subject Lesion Size en_US
dc.subject Mtor Inhibitor en_US
dc.subject Neurofibromatosis Type-1 en_US
dc.subject Nf-1 en_US
dc.title Effect of Everolimus on Prognosis of Neurofibromatosis Type 1 Lesions: a Systematic Review and Meta Analysis en_US
dc.type Review en_US
dspace.entity.type Publication
gdc.author.id Abdelkader, Rem/0009-0000-0900-3978
gdc.author.id Hanen, George Magdy Halim/0000-0002-8946-2046
gdc.author.id Alhamad, Mohammad/0000-0002-2175-1597
gdc.author.id Meshref, Mostafa/0000-0003-0692-6309
gdc.author.id Nashwan, Abdulqadir/0000-0003-4845-4119
gdc.author.id Ibrahim, Ismail/0000-0002-0805-8181
gdc.author.scopusid 59287713600
gdc.author.scopusid 59175615800
gdc.author.scopusid 59298384600
gdc.author.scopusid 59315962800
gdc.author.scopusid 59316670600
gdc.author.scopusid 59316670700
gdc.author.scopusid 57222069701
gdc.author.wosid Ibrahim, Ismail/KLC-4059-2024
gdc.author.wosid Meshref, Mostafa/F-7863-2019
gdc.author.wosid Nashwan, Abdulqadir/J-6241-2019
gdc.description.department Fenerbahçe University en_US
gdc.description.departmenttemp [Ibrahim, Ismail A.] Fenerbahce Univ, Fac Hlth Sci, Istanbul, Turkiye; [Abdelkader, Rem Ehab] Mansoura Univ, Mansoura Manchester Program Med Educ, Mansoura, Egypt; [Nada, Ahmed Hosney] Benha Univ, Fac Med, Banha, Egypt; [Younes, Siham; Hamad, Mohammad] Univ Jordan, Fac Med, Amman, Jordan; [Hanen, George] Minia Univ, Fac Med, Al Minya, Egypt; [Shahwan, Ghena] Hashemite Univ, Fac Med, Amman, Jordan; [Meshref, Mostafa] Al Azhar Univ, Fac Med, Dept Neurol, Cairo, Egypt; [Nashwan, Abdulqadir J.] Hamad Med Corp, POB 3050, Doha, Qatar en_US
gdc.description.endpage 869 en_US
gdc.description.issue 11 en_US
gdc.description.publicationcategory Diğer en_US
gdc.description.scopusquality Q2
gdc.description.startpage 865 en_US
gdc.description.volume 46 en_US
gdc.description.woscitationindex Science Citation Index Expanded
gdc.description.wosquality Q3
gdc.identifier.pmid 39244488
gdc.identifier.wos WOS:001366010400001
gdc.scopus.citedcount 0
gdc.wos.citedcount 0

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