| Literature DB >> 24631738 |
Corrado Girmenia1, Anna Maria Raiola2, Alfonso Piciocchi3, Alessandra Algarotti4, Marta Stanzani5, Laura Cudillo6, Clara Pecoraro7, Stefano Guidi8, Anna Paola Iori9, Barbara Montante10, Patrizia Chiusolo11, Edoardo Lanino12, Angelo Michele Carella13, Elisa Zucchetti14, Benedetto Bruno15, Giuseppe Irrera16, Francesca Patriarca17, Donatella Baronciani18, Maurizio Musso19, Arcangelo Prete20, Antonio Maria Risitano21, Domenico Russo22, Nicola Mordini23, Domenico Pastore24, Adriana Vacca25, Francesco Onida26, Sadia Falcioni27, Giovanni Pisapia28, Giuseppe Milone29, Daniele Vallisa30, Attilio Olivieri31, Alessandro Bonini32, Elio Castagnola12, Simona Sica11, Ignazio Majolino10, Alberto Bosi8, Alessandro Busca7, William Arcese6, Giuseppe Bandini5, Andrea Bacigalupo2, Alessandro Rambaldi4, Anna Locasciulli33.
Abstract
Epidemiologic investigation of invasive fungal diseases (IFDs) in allogeneic hematopoietic stem cell transplantation (allo-HSCT) may be useful to identify subpopulations who might benefit from targeted treatment strategies. The Gruppo Italiano Trapianto Midollo Osseo (GITMO) prospectively registered data on 1858 consecutive patients undergoing allo-HSCT between 2008 and 2010. Logistic regression analysis was performed to identify risk factors for proven/probable IFD (PP-IFD) during the early (days 0 to 40), late (days 41 to 100), and very late (days 101 to 365) phases after allo-HSCT and to evaluate the impact of PP-IFDs on 1-year overall survival. The cumulative incidence of PP-IFDs was 5.1% at 40 days, 6.7% at 100 days, and 8.8% at 12 months post-transplantation. Multivariate analysis identified the following variables as associated with PP-IFDs: transplant from an unrelated volunteer donor or cord blood, active acute leukemia at the time of transplantation, and an IFD before transplantation in the early phase; transplant from an unrelated volunteer donor or cord blood and grade II-IV acute graft-versus-host disease (GVHD) in the late phase; and grade II-IV acute GVHD and extensive chronic GVHD in the very late phase. The risk for PP-IFD was significantly higher when acute GVHD was followed by chronic GVHD and when acute GVHD occurred in patients undergoing transplantation with grafts from other than matched related donors. The presence of PP-IFD was an independent factor in long-term survival (hazard ratio, 2.90; 95% confidence interval, 2.32 to 3.62; P < .0001). Our findings indicate that tailored prevention strategies may be useful in subpopulations at differing levels of risk for PP-IFDs.Entities:
Keywords: Allogeneic HSCT; Epidemiology; Invasive fungal disease
Mesh:
Year: 2014 PMID: 24631738 DOI: 10.1016/j.bbmt.2014.03.004
Source DB: PubMed Journal: Biol Blood Marrow Transplant ISSN: 1083-8791 Impact factor: 5.742