Long-term follow-up of HCV-infected hematopoietic SCT patients and effects of antiviral therapy

This prospective study was initiated in 1993 with the aim to study late effects and responses to antiviral therapy in a cohort of hepatitis C virus (HCV)-infected patients. A total of 195 patients were included from 12 centers. In all, 134 patients had undergone allogeneic and 61 autologous hematopo...

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Veröffentlicht in:Bone marrow transplantation (Basingstoke) 2012-09, Vol.47 (9), p.1217-1221
Hauptverfasser: Ljungman, P, Locasciulli, A, de Soria, V G, Békássy, A N, Brinch, L, Espigado, I, Ferrant, A, Franklin, I M, O'Riordan, J, Rovira, M, Shaw, P, Einsele, H
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Sprache:eng
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Zusammenfassung:This prospective study was initiated in 1993 with the aim to study late effects and responses to antiviral therapy in a cohort of hepatitis C virus (HCV)-infected patients. A total of 195 patients were included from 12 centers. In all, 134 patients had undergone allogeneic and 61 autologous hematopoietic SCT (HSCT). The median follow-up from HSCT is currently 16.8 years and the maximum 27.2 years. Overall 33 of 195 patients have died of which 6 died from liver complications. The survival probability was 81.6% and the cumulative incidence for death in liver complications was 6.1% at 20 years after HSCT. The cumulative incidence of severe liver complications (death from liver failure, cirrhosis and liver transplantation) was 11.7% at 20 years after HSCT. In all, 85 patients have been treated with IFN; 42 in combination with ribavirin. The sustained response rate was 40%. The rates of severe side effects were comparable to other patient populations and no patient developed significant exacerbations of GVHD. Patients receiving antiviral therapy had a trend toward a decreased risk of severe liver complications (odds ratio=0.33; P =0.058). HCV infection is associated with morbidity and mortality in long-term survivors after HSCT. Antiviral therapy can be given safely and might reduce the risk for severe complications.
ISSN:0268-3369
1476-5365
1476-5365
DOI:10.1038/bmt.2011.238