Voriconazole for secondary prophylaxis of invasive fungal infections in allogeneic stem cell transplant recipients: results of the VOSIFI study
Autor: | Catherine, Cordonnier, Montserrat, Rovira, Johan, Maertens, Eduardo, Olavarria, Catherine, Faucher, Karin, Bilger, Arnaud, Pigneux, Oliver A, Cornely, Andrew J, Ullmann, Rodrigo Martino, Bofarull, Rafael, de la Cámara, Maja, Weisser, Effie, Liakopoulou, Manuel, Abecasis, Claus Peter, Heussel, Marc, Pineau, Per, Ljungman, Hermann, Einsele |
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Rok vydání: | 2010 |
Předmět: |
Adult
Male medicine.medical_specialty Antifungal Agents medicine.medical_treatment Hematopoietic stem cell transplantation Biology Aspergillosis Young Adult Internal medicine voriconazole medicine Humans Transplantation Homologous transplant Cumulative incidence Mycosis Aged allogeneic Voriconazole Leukemia Incidence Hematopoietic Stem Cell Transplantation Hematology Middle Aged Triazoles medicine.disease Surgery Transplantation Pyrimidines Treatment Outcome Mycoses fungal Chemoprophylaxis Female prophylaxis Zygomycosis medicine.drug |
Zdroj: | HAEMATOLOGICA r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau instname |
ISSN: | 1592-8721 0390-6078 |
Popis: | Background Recurrence of prior invasive fungal infection (relapse rate of 30-50%) limits the success of stem cell transplantation. Secondary prophylaxis could reduce disease burden and improve survival. Design and Methods A prospective, open-label, multicenter trial was conducted evaluating voriconazole (4 mg/kg/12 h intravenously or 200 mg/12 h orally) as secondary antifungal prophylaxis in allogeneic stem cell transplant recipients with previous proven or probable invasive fungal infection. Voriconazole was started 48 h or more after completion of conditioning chemotherapy and was planned to be continued for 100-150 days. Patients were followed for 12 months. The primary end-point of the study was the incidence of proven or probable invasive fungal infection. Results Forty-five patients were enrolled, 41 of whom had acute leukemia. Previous invasive fungal infections were proven or probable aspergillosis (n=31), proven candidiasis (n=5) and other proven or probable infections (n=6); prior infection could not be confirmed in three patients. The median duration of voriconazole prophylaxis was 94 days. Eleven patients (24%) died within 12 months of transplantation, but only one due to systemic fungal disease. Three invasive fungal infections occurred post-transplant: two relapses (one candidemia and one fatal scedosporiosis) and one new zygomycosis in a patient with previous aspergillosis. The 1-year cumulative incidence of invasive fungal disease was 6.7 3.6%. Two patients were withdrawn from the study due to treatment-related adverse events (i.e. liver toxicity). Conclusions Voriconazole appears to be safe and effective for secondary prophylaxis of systemic fungal infection after allogeneic stem cell transplantation. The observed incidence of 6.7% (with one attributable death) is considerably lower than the relapse rate reported in historical controls, thus suggesting that voriconazole is a promising prophylactic agent in this population. |
Databáze: | OpenAIRE |
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