Pulmonary infections (PIs) are a major complication of patients with myelodysplastic syndromes (MDS). We retrospectively evaluated 234 MDS patients treated with azacytidine (AZA). The total number of AZA cycles was 2886 (median 8 cycles per patient). There were 111 episodes of PI (3.8% of AZA cycles) in 81 patients (34.6%). PIs were considered of fungal origin in 27 cases (24.3%), associated to bacteremia in 11 cases (9.9%), to influenza infection in 2 cases (1.8%) and of unknown origin in the remaining 71 cases (64.0%). Forty-five PI episodes were documented in cycles 1-4 of AZA (5.1% of 875 cycles) and the remaining 66 episodes beyond the 4th cycle (3.2% of 2011 cycles) (p=0.017). Overall, a fungal PI was documented in 13/875 (1.5%) cycles 1-4 and in 13/2011 (0.6%) cycles beyond the 4th cycle (p=0.001). A baseline chronic pulmonary disease was significantly associated to a higher risk of severe PIs. In the survival analysis, cases of PI in patients who progressed to acute leukemia (PAL) were excluded, in view of the predominant influence of PAL on the outcome of the patients. A PI unrelated to PAL documented during the first 4 AZA cycles was an independent factor predicting lower survival (OR 2.13, 95% CI 1.37-3.33; p=0.001). In conclusion, PIs are common in MDS patients receiving AZA, in particular during the first cycles of treatment, and are associated with an unfavorable outcome. The results of our study raise the issue of the need of a tailored infection prevention strategy. This article is protected by copyright. All rights reserved.

Latagliata, R., Niscola, P., Fianchi, L., Aloe Spiriti, M.a., Maurillo, L., Carmosino, I., et al. (2019). Pulmonary Infections in Patients with Myelodysplastic Syndromes Receiving Frontline Azacytidine Treatment. HEMATOLOGICAL ONCOLOGY [10.1002/hon.2710].

Pulmonary Infections in Patients with Myelodysplastic Syndromes Receiving Frontline Azacytidine Treatment

Campagna, Alessia;Buccisano, Francesco;Voso, Maria Teresa;De Fabritiis, Paolo;
2019-01-01

Abstract

Pulmonary infections (PIs) are a major complication of patients with myelodysplastic syndromes (MDS). We retrospectively evaluated 234 MDS patients treated with azacytidine (AZA). The total number of AZA cycles was 2886 (median 8 cycles per patient). There were 111 episodes of PI (3.8% of AZA cycles) in 81 patients (34.6%). PIs were considered of fungal origin in 27 cases (24.3%), associated to bacteremia in 11 cases (9.9%), to influenza infection in 2 cases (1.8%) and of unknown origin in the remaining 71 cases (64.0%). Forty-five PI episodes were documented in cycles 1-4 of AZA (5.1% of 875 cycles) and the remaining 66 episodes beyond the 4th cycle (3.2% of 2011 cycles) (p=0.017). Overall, a fungal PI was documented in 13/875 (1.5%) cycles 1-4 and in 13/2011 (0.6%) cycles beyond the 4th cycle (p=0.001). A baseline chronic pulmonary disease was significantly associated to a higher risk of severe PIs. In the survival analysis, cases of PI in patients who progressed to acute leukemia (PAL) were excluded, in view of the predominant influence of PAL on the outcome of the patients. A PI unrelated to PAL documented during the first 4 AZA cycles was an independent factor predicting lower survival (OR 2.13, 95% CI 1.37-3.33; p=0.001). In conclusion, PIs are common in MDS patients receiving AZA, in particular during the first cycles of treatment, and are associated with an unfavorable outcome. The results of our study raise the issue of the need of a tailored infection prevention strategy. This article is protected by copyright. All rights reserved.
2019
Online ahead of print
Rilevanza internazionale
Articolo
Esperti anonimi
Settore MED/15 - MALATTIE DEL SANGUE
English
Myelodysplastic Syndromes; azacytidine; prognosis; pulmonary infections
Latagliata, R., Niscola, P., Fianchi, L., Aloe Spiriti, M.a., Maurillo, L., Carmosino, I., et al. (2019). Pulmonary Infections in Patients with Myelodysplastic Syndromes Receiving Frontline Azacytidine Treatment. HEMATOLOGICAL ONCOLOGY [10.1002/hon.2710].
Latagliata, R; Niscola, P; Fianchi, L; Aloe Spiriti, Ma; Maurillo, L; Carmosino, I; Cesini, L; Sarlo, C; Piccioni, A; Campagna, A; De Luca, Ml; De Benedittis, D; Mancini, M; Breccia, M; Criscuolo, M; Buccisano, F; Voso, Mt; Avvisati, G; Tafuri, A; De Fabritiis, P; Foà, R; Girmenia, C
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2108/226581
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