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1.
Pediatr Transplant ; 24(1): e13625, 2020 02.
Artículo en Inglés | MEDLINE | ID: mdl-31821668

RESUMEN

X-linked agammaglobulinemia (XLA) is a primary antibody disorder due to a mutation in the Bruton tyrosine kinase gene that requires lifelong immunoglobulin replacement resulting in a significant economic burden and treatment abandonment. Hematopoietic stem cell transplantation (HSCT) offers an alternative option for complete cure. In our series, two children with XLA underwent successful HSCT using a myeloablative conditioning with thiotepa, treosulfan, and fludarabine from a matched sibling donor. The second child had rejected his first graft following a busulfan-based regimen with resultant autologous reconstitution. At 6 months post-HSCT, serum IgG were normal, off IVIG, and had no infections. Both children after a median follow-up of 20 months have 100% chimerism. Treosulfan-based reduced toxicity myeloablative HSCT has encouraging results with a positive impact on the socioeconomics in developing countries.


Asunto(s)
Agammaglobulinemia/terapia , Busulfano/análogos & derivados , Análisis Costo-Beneficio , Países en Desarrollo , Enfermedades Genéticas Ligadas al Cromosoma X/terapia , Trasplante de Células Madre Hematopoyéticas/métodos , Inmunosupresores/uso terapéutico , Acondicionamiento Pretrasplante/métodos , Agammaglobulinemia/economía , Busulfano/uso terapéutico , Quimioterapia Combinada , Enfermedades Genéticas Ligadas al Cromosoma X/economía , Trasplante de Células Madre Hematopoyéticas/economía , Humanos , Inmunoglobulinas Intravenosas/economía , Inmunoglobulinas Intravenosas/uso terapéutico , India , Lactante , Masculino , Acondicionamiento Pretrasplante/efectos adversos , Acondicionamiento Pretrasplante/economía
2.
Clin Drug Investig ; 38(10): 955-965, 2018 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-30191508

RESUMEN

BACKGROUND: In Italy, there is scarce evidence on the epidemiological and economic burden induced by primary antibody deficiencies. OBJECTIVE: The aim of this study was to elaborate the available epidemiological and cost data in order to estimate the annual expenditure induced by the management of patients affected by the common variable immunodeficiency (CVID) and X-linked agammaglobulinemia (XLA) requiring immunoglobulin (Ig) replacement therapy. METHODS: A probabilistic cost-of-illness model was developed to estimate the number of patients with CVID and XLA, and the economic burden associated with their therapy in terms of direct or indirect costs. A systematic literature review was carried out to reveal both epidemiological and economic data. Furthermore, a probabilistic sensitivity analysis with 5000 Monte Carlo simulations was performed. RESULTS: The epidemiological model allowed us to estimate the number of prevalent patients affected by XLA and CVID in Italy in 2017, corresponding to 1885 (95% confidence interval [CI] 944-3145) and 133 (95% CI 115-152) patients, respectively. The estimated total expenditure for the treatment and management of patients with CVID and XLA requiring Ig replacement therapy amounts to €42.68 million (95% CI €14.38-€86.1 million). CONCLUSIONS: This information provides a comprehensive perspective of the economic issues, and facilitates better-informed public health decision making, in the management of CVID and XLA in Italy.


Asunto(s)
Agammaglobulinemia/tratamiento farmacológico , Inmunodeficiencia Variable Común/tratamiento farmacológico , Costo de Enfermedad , Enfermedades Genéticas Ligadas al Cromosoma X/tratamiento farmacológico , Inmunoglobulinas/administración & dosificación , Adolescente , Adulto , Agammaglobulinemia/economía , Agammaglobulinemia/epidemiología , Inmunodeficiencia Variable Común/economía , Inmunodeficiencia Variable Común/epidemiología , Femenino , Enfermedades Genéticas Ligadas al Cromosoma X/economía , Enfermedades Genéticas Ligadas al Cromosoma X/epidemiología , Humanos , Inmunoglobulinas/economía , Italia/epidemiología , Masculino , Persona de Mediana Edad , Método de Montecarlo , Prevalencia , Adulto Joven
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