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Time between inhibitor detection and start of immune tolerance induction: Association with outcome in the BrazIT study.
Camelo, Ricardo Mesquita; Dias, Maíse Moreira; Caram-Deelder, Camila; Gouw, Samantha; de Magalhães, Laura Peixoto; Zuccherato, Luciana Werneck; Jardim, Letícia Lemos; de Oliveira, Andrea Gonçalves; de Albuquerque Ribeiro, Rosângela; Franco, Vivian Karla Brognoli; do Rosário Ferraz Roberti, Maria; de Araújo Callado, Fábia Michelle Rodrigues; Etto, Leina Yukari; de Cerqueira, Maria Aline Ferreira; Cerqueira, Mônica Hermida; Lorenzato, Cláudia Santos; de Souza, Ieda Solange; Serafim, Édvis Santos Soares; Garcia, Andrea Aparecida; Anegawa, Tânia Hissa; Neves, Daniele Campos Fontes; Tan, Doralice Marvulle; van der Bom, Johanna; Rezende, Suely Meireles.
Afiliação
  • Camelo RM; Faculty of Medicine, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.
  • Dias MM; Department of Clinical Epidemiology, Leiden University Medical Center, Leiden, the Netherlands.
  • Caram-Deelder C; Faculty of Medicine, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.
  • Gouw S; Department of Clinical Epidemiology, Leiden University Medical Center, Leiden, the Netherlands.
  • de Magalhães LP; Center of Clinical Transfusion Research, Sanquin Research, Leiden, The Netherlands.
  • Zuccherato LW; Amsterdam UMC, University of Amsterdam, Department of Pediatric Hematology, Amsterdam, the Netherlands.
  • Jardim LL; Faculty of Medicine, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.
  • de Oliveira AG; Faculty of Medicine, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.
  • de Albuquerque Ribeiro R; Faculty of Medicine, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.
  • Franco VKB; Department of Clinical Epidemiology, Leiden University Medical Center, Leiden, the Netherlands.
  • do Rosário Ferraz Roberti M; Fundação HEMOMINAS, Belo Horizonte, Brazil.
  • de Araújo Callado FMR; Centro de Hematologia e Hemoterapia do Ceará (HEMOCE), Fortaleza, Brazil.
  • Etto LY; Hospital Universitário Walter Cantídeo, Universidade Federal do Ceará, Fortaleza, Brazil.
  • de Cerqueira MAF; Centro de Hematologia e Hemoterapia de Santa Catarina (HEMOSC), Florianópolis, Brazil.
  • Cerqueira MH; Hemocentro de Goiás (HEMOGO), Goiânia, Brazil.
  • Lorenzato CS; Faculty of Medicine, Universidade Federal de Goiás, Goiânia, Brazil.
  • de Souza IS; Fundação de Hematologia e Hemoterapia de Pernambuco (HEMOPE), Recife, Brazil.
  • Serafim ÉSS; Hemocentro da Paraíba (HEMOÍBA), João Pessoa, Brazil.
  • Garcia AA; Department of Internal Medicine, Center of Medical Sciences, Universidade Federal da Paraíba, João Pessoa, Brazil.
  • Anegawa TH; Centro de Hematologia e Hemoterapia do Piauí (HEMOPI), Teresina, Brazil.
  • Neves DCF; Instituto de Hematologia do Estado do Rio de Janeiro (HEMORIO), Rio de Janeiro, Brazil.
  • Tan DM; Coagulopathy Clinic, Hemocentro do Paraná (HEMEPAR), Curitiba, Brazil.
  • van der Bom J; Department of Clinical Haematology, Centro de Hematologia e Hemoterapia do Pará (HEMOPA), Belém, Brazil.
  • Rezende SM; Universitary Hospital João de Barros Barreto, Universidade Federal do Pará, Belém, Brazil.
J Thromb Haemost ; 20(11): 2526-2537, 2022 11.
Article em En | MEDLINE | ID: mdl-36102352
ABSTRACT

BACKGROUND:

Immune tolerance induction (ITI) is the treatment of choice for eradication of anti-factor VIII (FVIII) neutralizing alloantibodies (inhibitors) in people with inherited hemophilia A and high-responding inhibitor (PwHA-HRi). The association between ITI outcome and time elapsed between inhibitor detection and start of ITI (∆tinhi-ITI ) is debatable.

OBJECTIVE:

The aim of this study was to evaluate this association among a large cohort of severe PwHA-HRi.

METHODS:

Severe (factor VIII activity level <1%) PwHA-HRi on ITI (n = 142) were enrolled in 15 hemophilia treatment centers. PwHA-HRi were treated according to the Brazilian ITI Protocol. ITI outcomes were defined as success (i.e., recovered responsiveness to exogenous FVIII) and failure (i.e., no responsiveness to exogenous FVIII and requirement of bypassing agents to control bleeding).

RESULTS:

Median ages at inhibitor detection and at ITI start were 3.2 years (interquartile range [IQR], 1.6-8.1) and 6.9 years [IQR, 2.6-20.1), respectively. PwHA-HRi were stratified according to ∆tinhi-ITI quartiles first (0.0-0.6 year), second (>0.6-1.7 year), third (>1.7-9.2 years), and fourth quartile (>9.2-24.5 years). The overall success rate was 65.5% (93/142), with no difference among first, second, third, and fourth quartiles (62.9%, 69.4%, 58.3%, and 71.4%, respectively) even after adjusting the analyses for potential confounders.

CONCLUSION:

In conclusion, delayed ITI start is not associated with failure of ITI in PwHA-HRi. Therefore, ITI should be offered for these patients, regardless of the time elapsed between the detection of inhibitor and the ITI start.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Hemostáticos / Hemofilia A Tipo de estudo: Diagnostic_studies / Guideline / Risk_factors_studies Limite: Child / Child, preschool / Humans / Infant Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Hemostáticos / Hemofilia A Tipo de estudo: Diagnostic_studies / Guideline / Risk_factors_studies Limite: Child / Child, preschool / Humans / Infant Idioma: En Ano de publicação: 2022 Tipo de documento: Article