Acquired hemophilia A (AHA) is an autoimmune disease caused by an autoantibody to factor VIII. Patients are at risk of severe and fatal hemorrhage until the inhibitor is eradicated, and guidelines recommend immunosuppression as soon as the diagnosis has been made. The optimal immunosuppressive regimen is unclear; therefore, data from 331 patients entered into the prospective EACH2 registry were analyzed. Steroids combined with cyclophosphamide resulted in more stable complete remission (70%), defined as inhibitor undetectable, factor VIII more than 70 IU/dL and immunosuppression stopped, than steroids alone (48%) or rituximab-based regimens (59%). Propensity score-matched analysis controlling for age, sex, factor VIII level, inhibitor titer, and underlying etiology confirmed that stable remission was more likely with steroids and cyclophosphamide than steroids alone (odds ratio = 3.25; 95% CI, 1.51-6.96; P < .003). The median time to complete remission was approximately 5 weeks for steroids with or without cyclophosphamide; rituximab-based regimens required approximately twice as long. Immunoglobulin administration did not improve outcome. Second-line therapy was successful in approximately 60% of cases that failed first-line therapy. Outcome was not affected by the choice of first-line therapy. The likelihood of achieving stable remission was not affected by underlying etiology but was influenced by the presenting inhibitor titer and FVIII level.

Immunosuppression for acquired hemophilia A: results from the European Acquired Haemophilia Registry (EACH2) / Collins, P; Baudo, F; Knoebl, P; Lévesque, H; Nemes, L; Pellegrini, F; Marco, P; Tengborn, L; Huth Kühne, A; EACH2 registry, Collaborators; Mazzucconi, Maria Gabriella; Santoro, Cristina. - In: BLOOD. - ISSN 0006-4971. - ELETTRONICO. - 120:1(2012), pp. 47-55. [10.1182/blood-2012-02-409185]

Immunosuppression for acquired hemophilia A: results from the European Acquired Haemophilia Registry (EACH2).

MAZZUCCONI, Maria Gabriella;SANTORO, Cristina
2012

Abstract

Acquired hemophilia A (AHA) is an autoimmune disease caused by an autoantibody to factor VIII. Patients are at risk of severe and fatal hemorrhage until the inhibitor is eradicated, and guidelines recommend immunosuppression as soon as the diagnosis has been made. The optimal immunosuppressive regimen is unclear; therefore, data from 331 patients entered into the prospective EACH2 registry were analyzed. Steroids combined with cyclophosphamide resulted in more stable complete remission (70%), defined as inhibitor undetectable, factor VIII more than 70 IU/dL and immunosuppression stopped, than steroids alone (48%) or rituximab-based regimens (59%). Propensity score-matched analysis controlling for age, sex, factor VIII level, inhibitor titer, and underlying etiology confirmed that stable remission was more likely with steroids and cyclophosphamide than steroids alone (odds ratio = 3.25; 95% CI, 1.51-6.96; P < .003). The median time to complete remission was approximately 5 weeks for steroids with or without cyclophosphamide; rituximab-based regimens required approximately twice as long. Immunoglobulin administration did not improve outcome. Second-line therapy was successful in approximately 60% of cases that failed first-line therapy. Outcome was not affected by the choice of first-line therapy. The likelihood of achieving stable remission was not affected by underlying etiology but was influenced by the presenting inhibitor titer and FVIII level.
2012
01 Pubblicazione su rivista::01a Articolo in rivista
Immunosuppression for acquired hemophilia A: results from the European Acquired Haemophilia Registry (EACH2) / Collins, P; Baudo, F; Knoebl, P; Lévesque, H; Nemes, L; Pellegrini, F; Marco, P; Tengborn, L; Huth Kühne, A; EACH2 registry, Collaborators; Mazzucconi, Maria Gabriella; Santoro, Cristina. - In: BLOOD. - ISSN 0006-4971. - ELETTRONICO. - 120:1(2012), pp. 47-55. [10.1182/blood-2012-02-409185]
File allegati a questo prodotto
Non ci sono file associati a questo prodotto.

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/498104
 Attenzione

Attenzione! I dati visualizzati non sono stati sottoposti a validazione da parte dell'ateneo

Citazioni
  • ???jsp.display-item.citation.pmc??? 80
  • Scopus 250
  • ???jsp.display-item.citation.isi??? 226
social impact