Innovative solutions? Belzutifan therapy for hemangioblastomas in Von Hippel-Lindau disease: A systematic review and single-arm meta-analysis.

Belzutifan Hemangioblastoma Von Hippel-Lindau disease

Journal

Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia
ISSN: 1532-2653
Titre abrégé: J Clin Neurosci
Pays: Scotland
ID NLM: 9433352

Informations de publication

Date de publication:
10 Aug 2024
Historique:
received: 08 07 2024
revised: 31 07 2024
accepted: 03 08 2024
medline: 12 8 2024
pubmed: 12 8 2024
entrez: 11 8 2024
Statut: aheadofprint

Résumé

Von Hippel-Lindau (VHL) disease is a rare autosomal dominant disorder that predisposes patients to develop multiple cysts and tumors, such as hemangioblastomas (HBs) and clear cell renal cell carcinoma (ccRCC), due to mutations in the VHL tumor suppressor gene. While treatment of HBs varies based on their characteristics and has improved patient survival, it still involves high morbidity and mortality, leading to ongoing debates and studies to refine therapy strategies. Recent developments include the emergence of Belzutifan, a novel inhibitor targeting hypoxia-inducible factor 2α (HIF-2α), which has shown promising results in ongoing trials, particularly for patients not immediately requiring surgery. This systematic review and meta-analysis aimed to comprehensively evaluate the efficacy and safety of Belzutifan for treating HBs associated with VHL disease. Search was conducted across Medline, Embase, Cochrane, and Web of Science databases. Statistical Analysis was performed, with proportions and 95 % confidence intervals. Statistical analyses were carried out using R Studio. Ten studies were selected, comprising 553 patients. The population mean age was 40 (24-65), and 50 % of the population was formed by males. In terms of proportion, 6 analyses were performed: Disease Stability of 31 % [95 %CI:14 %-47 %; I2 = 2 %]; Disease Progression of 2 %[95 %CI:0 %-9 %; I2 = 0 %]; Partial Response of 75 % [95 %CI:54 %-96 %; I2 = 58 %]. Complete response of 1 % [95 %CI:0 %-7 %; I2 = 0 %];and Side effects, anemia 81 % rate [95 % CI:54 %-100 %; I2 = 94 %], and fatigue rate of 79 % [95 % CI:54 %-100 %;I2 = 94 %]. Results indicate that Belzutifan effectively stabilizes disease, reduces tumor progression, and achieves significant therapeutic responses, although side effects like anemia and fatigue were noted.

Sections du résumé

BACKGROUND BACKGROUND
Von Hippel-Lindau (VHL) disease is a rare autosomal dominant disorder that predisposes patients to develop multiple cysts and tumors, such as hemangioblastomas (HBs) and clear cell renal cell carcinoma (ccRCC), due to mutations in the VHL tumor suppressor gene. While treatment of HBs varies based on their characteristics and has improved patient survival, it still involves high morbidity and mortality, leading to ongoing debates and studies to refine therapy strategies. Recent developments include the emergence of Belzutifan, a novel inhibitor targeting hypoxia-inducible factor 2α (HIF-2α), which has shown promising results in ongoing trials, particularly for patients not immediately requiring surgery.
METHODS METHODS
This systematic review and meta-analysis aimed to comprehensively evaluate the efficacy and safety of Belzutifan for treating HBs associated with VHL disease. Search was conducted across Medline, Embase, Cochrane, and Web of Science databases. Statistical Analysis was performed, with proportions and 95 % confidence intervals. Statistical analyses were carried out using R Studio.
RESULTS RESULTS
Ten studies were selected, comprising 553 patients. The population mean age was 40 (24-65), and 50 % of the population was formed by males. In terms of proportion, 6 analyses were performed: Disease Stability of 31 % [95 %CI:14 %-47 %; I2 = 2 %]; Disease Progression of 2 %[95 %CI:0 %-9 %; I2 = 0 %]; Partial Response of 75 % [95 %CI:54 %-96 %; I2 = 58 %]. Complete response of 1 % [95 %CI:0 %-7 %; I2 = 0 %];and Side effects, anemia 81 % rate [95 % CI:54 %-100 %; I2 = 94 %], and fatigue rate of 79 % [95 % CI:54 %-100 %;I2 = 94 %].
CONCLUSION CONCLUSIONS
Results indicate that Belzutifan effectively stabilizes disease, reduces tumor progression, and achieves significant therapeutic responses, although side effects like anemia and fatigue were noted.

Identifiants

pubmed: 39128437
pii: S0967-5868(24)00313-8
doi: 10.1016/j.jocn.2024.110774
pii:
doi:

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

110774

Informations de copyright

Copyright © 2024. Published by Elsevier Ltd.

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

Lucca B Palavani (LB)

Max Planck University Center, Indaiatuba, São Paulo, SP, Brazil.

Raphael Camerotte (R)

Federal University of Rio de Janeiro, Rio de Janeiro, RJ, Brazil.

Bernardo Vieira Nogueira (B)

Serra dos Órgãos University Center, Teresópolis, RJ, Brazil. Electronic address: bevnogueira@gmail.com.

Márcio Yuri Ferreira (MY)

Department of Neurosurgery, Lenox Hill Hospital/Northwell Health, New York, NY, USA.

Leonardo B Oliveira (LB)

Department of Neurosurgery, State University of Ponta Grossa, Ponta Grossa, PR, Brazil.

Lucas Pari Mitre (L)

Santa Casa de São Paulo School of Medical Sciences, São Paulo, SP, Brazil.

Wilson Coelho Nogueira de Castro (W)

State University of Piauí, Teresina, PI, Brazil.

Gisele Lúcia Canto Gomes (GL)

Federal University of Amazonas, Manaus, AM, Brazil.

Luis F Fabrini Paleare (LF)

School of Medicine, Pontifical Catholic University of Paraná, Curitiba, PR, Brazil.

Sávio Batista (S)

Federal University of Rio de Janeiro, Rio de Janeiro, RJ, Brazil.

Filipi Fim Andreão (F)

Federal University of Rio de Janeiro, Rio de Janeiro, RJ, Brazil.

Raphael Bertani (R)

Department of Neurosurgery, University of São Paulo, São Paulo, SP, Brazil.

Allan Dias Polverini (A)

Neurosurgical Oncology Division, Barretos Cancer Hospital, Barretos, SP, Brazil.

Classifications MeSH