Journal of Pediatric Neurology 2024; 22(04): 277-286
DOI: 10.1055/s-0043-1778099
Original Article

The Impact of Pabinafusp Alfa on the Disease Burden in Hunter's Syndrome: Patient-Reported Outcomes

Ana Maria Martins
1   Centro de Referências em Erros Inatos do Metabolismo (CREIM), Universidade Federal de São Paulo (UNIFESP), São Paulo, Brazil
,
Marco Antônio Curiati
1   Centro de Referências em Erros Inatos do Metabolismo (CREIM), Universidade Federal de São Paulo (UNIFESP), São Paulo, Brazil
,
Carmen Curiati Mendes
1   Centro de Referências em Erros Inatos do Metabolismo (CREIM), Universidade Federal de São Paulo (UNIFESP), São Paulo, Brazil
,
Edna Tiemi Sakata
1   Centro de Referências em Erros Inatos do Metabolismo (CREIM), Universidade Federal de São Paulo (UNIFESP), São Paulo, Brazil
,
Carolina Fischinger Moura de Souza
2   Serviço de Genética Médica, Hospital de Clínicas de Porto Alegre, Rio Grande do Sul, Brazil
3   Casa dos Raros, Porto Alegre, Rio Grande do Sul, Brazil
,
Roberto Giugliani
2   Serviço de Genética Médica, Hospital de Clínicas de Porto Alegre, Rio Grande do Sul, Brazil
3   Casa dos Raros, Porto Alegre, Rio Grande do Sul, Brazil
4   Programa de Pós-graduação em Genética e Biologia Molecular da Universidade Federal do Rio Grande do Sul, Rio Grande do Sul, Brazil
5   Dasa Genômica, São Paulo, Brazil
6   Instituto Nacional de Genética Populacional NAGEMP, Porto Alegre, Rio Grande do Sul, Brazil
› Institutsangaben

Funding Financial support has been provided to support medical writing of the manuscript by JCR Pharmaceuticals, but the publication was developed independently by the authors who are entirely responsible for the scientific content of the manuscript. Camilla Patti provided medical writer services for the elaboration of this manuscript.
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Abstract

Severe mucopolysaccharidosis type II (MPS-II) patients present with progressive mental impairment and reduced life expectancy. While current available treatment cannot cross the blood–brain barrier, the enzyme replacement therapy with pabinafusp alfa (a recombinant iduronate-2-sulfatase fused to an antihuman transferrin receptor antibody) was designed to penetrate it using transferrin receptor-mediated transcytosis. In this cross-sectional retrospective study, we aimed to report the impact of this new therapy using patient-reported outcomes. Data were collected using standardized questionnaire replied by patients or their caregivers (as proxies). Nine patients received intravenous administration of pabinafusp alfa for at least 104 weeks. All patient showed improvements in behavior (mainly aggressiveness), speech, motor ability, muscle strength, facial expression, breathing, and cognitive skills. Gait improvement was also found in 78% of participants. Caregivers also reported improvements in emotion demonstration as ability to smile, establish eye contact, and give hugs. Collectively, our results indicate a positive impact of pabinafusp alfa on quality of life of individuals with MPS-II and their relatives/caregivers. Future studies are warranted to elucidate the mechanisms underlying these beneficial effects.

Informed Consent

All procedures followed were in accordance with the ethical standards of the responsible committee on human experimentation (institutional and national) and with the Declaration of Helsinki 2013, as revised in 2000. The Ethics Committee from the Universidade Federal de São Paulo approved the study under the #0613/2018 protocol. Written informed consent for publication were obtained from the patients or the legal responsible of the patients.


Animal Rights

This article does not contain any studies with animal subjects performed by any of the authors.


Authors' Contributions

A.M.M., M.A.C., C.C.M., and E.T.S. conceived and designed the manuscript and conducted data collection and analysis. All authors revised the text critically and approved the final manuscript.




Publikationsverlauf

Eingereicht: 16. April 2023

Angenommen: 04. Dezember 2023

Artikel online veröffentlicht:
01. März 2024

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