TY - JOUR
T1 - High Incidence of Invasive Fungal Diseases in Patients with FLT3-Mutated AML Treated with Midostaurin: Results of a Multicenter Observational SEIFEM Study
AU - Cattaneo, Chiara
AU - Marchesi, Francesco
AU - Terrenato, Irene
AU - Bonuomo, Valentina
AU - Fracchiolla, Nicola Stefano
AU - Delia, Mario
AU - Criscuolo, Marianna
AU - Candoni, Anna
AU - Prezioso, Lucia
AU - Facchinelli, Davide
AU - Pasciolla, Crescenza
AU - Del Principe, Maria Ilaria
AU - Dargenio, Michelina
AU - Buquicchio, Caterina
AU - Mitra, Maria Enza
AU - Farina, Francesca
AU - Borlenghi, Erika
AU - Nadali, Gianpaolo
AU - Gagliardi, Vito Pier
AU - Fianchi, Luana
AU - Sciumè, Mariarita
AU - Menna, Pierantonio
AU - Busca, Alessandro
AU - Rossi, Giuseppe
AU - Pagano, Livio
PY - 2022
Y1 - 2022
N2 - The potential drug-drug interactions of midostaurin may impact the choice of antifungal (AF) prophylaxis in FLT3-positive acute myeloid leukemia (AML) patients. To evaluate the incidence of invasive fungal diseases (IFD) during the treatment of FLT3-mutated AML patients and to correlate it to the different AF prophylaxis strategies, we planned a multicenter observational study involving 15 SEIFEM centers. One hundred fourteen patients treated with chemotherapy + midostaurin as induction/reinduction, consolidation or both were enrolled. During induction, the incidence of probable/proven and possible IFD was 10.5% and 9.7%, respectively; no statistically significant difference was observed according to the different AF strategy adopted. The median duration of neutropenia was similar in patients with or without IFD. Proven/probable and possible IFD incidence was 2.4% and 1.8%, respectively, during consolidation. Age was the only risk factor for IFD (OR, 95% CI, 1.10 [1.03–1.19]) and complete remission achievement after first induction the only one for survival (OR, 95% CI, 5.12 [1.93–13.60]). The rate of midostaurin discontinuation was similar across different AF strategies. The IFD attributable mortality during induction was 8.3%. In conclusion, the 20.2% overall incidence of IFD occurring in FLT3-mutated AML during induction with chemotherapy + midostaurin, regardless of AF strategy type, was noteworthy, and merits further study, particularly in elderly patients.
AB - The potential drug-drug interactions of midostaurin may impact the choice of antifungal (AF) prophylaxis in FLT3-positive acute myeloid leukemia (AML) patients. To evaluate the incidence of invasive fungal diseases (IFD) during the treatment of FLT3-mutated AML patients and to correlate it to the different AF prophylaxis strategies, we planned a multicenter observational study involving 15 SEIFEM centers. One hundred fourteen patients treated with chemotherapy + midostaurin as induction/reinduction, consolidation or both were enrolled. During induction, the incidence of probable/proven and possible IFD was 10.5% and 9.7%, respectively; no statistically significant difference was observed according to the different AF strategy adopted. The median duration of neutropenia was similar in patients with or without IFD. Proven/probable and possible IFD incidence was 2.4% and 1.8%, respectively, during consolidation. Age was the only risk factor for IFD (OR, 95% CI, 1.10 [1.03–1.19]) and complete remission achievement after first induction the only one for survival (OR, 95% CI, 5.12 [1.93–13.60]). The rate of midostaurin discontinuation was similar across different AF strategies. The IFD attributable mortality during induction was 8.3%. In conclusion, the 20.2% overall incidence of IFD occurring in FLT3-mutated AML during induction with chemotherapy + midostaurin, regardless of AF strategy type, was noteworthy, and merits further study, particularly in elderly patients.
KW - acute myeloid leukemia
KW - antifungal prophylaxis
KW - invasive fungal disease
KW - midostaurin
KW - acute myeloid leukemia
KW - antifungal prophylaxis
KW - invasive fungal disease
KW - midostaurin
UR - http://hdl.handle.net/10807/223789
U2 - 10.3390/jof8060583
DO - 10.3390/jof8060583
M3 - Article
SN - 2309-608X
VL - 8
SP - 583
EP - 590
JO - Journal of Fungi
JF - Journal of Fungi
ER -