Author: Mariotti, Jacopo; De Philippis, Chiara; Bramanti, Stefania; Sarina, Barbara; Tordato, Federica; Pocaterra, Daria; Casari, Erminia; Carloâ€Stella, Carmelo; Santoro, Armando; Castagna, Luca
Title: Caspofungin for primary antifungal prophylaxis after Tâ€cell–replete haploidentical stem cell transplantation with postâ€transplant cyclophosphamide Cord-id: saav639i Document date: 2019_2_13
ID: saav639i
Snippet: OBJECTIVES: Tâ€cell–replete haploidentical stem cell transplantation (Haploâ€SCT) with postâ€transplant cyclophosphamide (PTâ€Cy) is at high risk of invasive fungal infections (IFI), and antiâ€mold–active drug is required for primary antifungal prophylaxis (PAP) according to international guidelines. No data are available on the efficacy of caspofungin as PAP in this setting. METHODS: Here, we report our retrospective experience with 103 consecutive patients treated with caspofungin as
Document: OBJECTIVES: Tâ€cell–replete haploidentical stem cell transplantation (Haploâ€SCT) with postâ€transplant cyclophosphamide (PTâ€Cy) is at high risk of invasive fungal infections (IFI), and antiâ€mold–active drug is required for primary antifungal prophylaxis (PAP) according to international guidelines. No data are available on the efficacy of caspofungin as PAP in this setting. METHODS: Here, we report our retrospective experience with 103 consecutive patients treated with caspofungin as PAP after Haploâ€SCT. Caspofungin was administered only during the preâ€engraftment phase. RESULTS: Hundredâ€day cumulative incidence of provenâ€probable IFI (PPâ€IFI) was 8.7% and median day of onset was 19 postâ€SCT. No patient died of PPâ€IFI, and overall survival (OS) and nonâ€relapse mortality (NRM) hazard ratio (HR) for patients experiencing IFI were 1.02 (P = 0.9) and 0.7 (P = 0.7), respectively. Threeâ€year overall survival (OS) and 1â€year nonâ€relapse mortality (NRM) were 55% and 19%, respectively. By univariate analysis, duration of neutropenic phase and partial remission preâ€transplant disease status were associated with increased incidence of IFI, but were not confirmed by multivariate analysis. CONCLUSION: In summary, PAP with caspofungin is an effective strategy for preventing IFI in the context of Haploâ€SCT with PTâ€Cy. Further efforts are required in order to identify more potent strategies able to avoid the occurrence of breakthrough infections.
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