TY - JOUR
T1 - Prognostic impact and risk factors of infections in patients with chronic lymphocytic leukemia treated with ibrutinib
AU - Mauro, Francesca Romana
AU - Giannarelli, Diana
AU - Visentin, Andrea
AU - Reda, Gianluigi
AU - Sportoletti, Paolo
AU - Frustaci, Anna Maria
AU - Chiarenza, Annalisa
AU - Ciolli, Stefania
AU - Vitale, Candida
AU - Laurenti, Luca
AU - De Paoli, Lorenzo
AU - Murru, Roberta
AU - Gentile, Massimo
AU - Gentile, Marino
AU - Rigolin, Gian Matteo
AU - Levato, Luciano
AU - Giordano, Annamaria
AU - Giordano, Alessandro
AU - Del Poeta, Giovanni
AU - Stelitano, Caterina
AU - Ielo, Claudia
AU - Noto, Alessandro
AU - Guarente, Valerio
AU - Molica, Stefano
AU - Molica, Serena
AU - Coscia, Marta
AU - Tedeschi, Alessandra
AU - Gaidano, Gianluca
AU - Cuneo, Antonio
AU - Foà, Robin
AU - Foa, Robin
AU - Martelli, Maurizio
AU - Martelli, Maddalena
AU - Girmenia, Corrado
AU - Gentile, Giuseppe
AU - Trentin, Livio
PY - 2021
Y1 - 2021
N2 - Ibrutinib represents extraordinary progress in the treatment of chronic lymphocytic leukemia (CLL). However, treatment-related adverse events limit the benefit of this agent. This obser-vational, multicenter study focused on the incidence, risk factors, and prognostic impact of infections in 494 patients with CLL treated with an ibrutinib-based treatment. Ibrutinib was given to 89 (18%) previously untreated patients (combined with rituximab, 24) and 405 (82%) relapsed/refractory patients. Pneumonia (PN), grade ≥3 non-opportunistic infections (NOI), and opportunistic infections (OI) were recorded in 32% of patients with an overall incidence rate per 100 person-year of 15.3% (PN, 10%; NOI, 3.3%; OI, 2%). Infections were the reason for the permanent discontinuation of ibrutinib in 9% of patients. Patients who experienced pneumonia or a severe infection showed a significantly inferior survival than those who were infection-free (p < 0.0001). A scoring system based on the three factors associated with a significant and independent impact on infections—PN or severe infection in the year before starting ibrutinib, chronic obstructive pulmonary disease, ≥2 prior treatments—identified patients with a two-to threefold increase in the rate of infections. In conclusion, the results of this study highlight the adverse impact of infectious events on the outcomes of CLL patients treated with ibrutinib.
AB - Ibrutinib represents extraordinary progress in the treatment of chronic lymphocytic leukemia (CLL). However, treatment-related adverse events limit the benefit of this agent. This obser-vational, multicenter study focused on the incidence, risk factors, and prognostic impact of infections in 494 patients with CLL treated with an ibrutinib-based treatment. Ibrutinib was given to 89 (18%) previously untreated patients (combined with rituximab, 24) and 405 (82%) relapsed/refractory patients. Pneumonia (PN), grade ≥3 non-opportunistic infections (NOI), and opportunistic infections (OI) were recorded in 32% of patients with an overall incidence rate per 100 person-year of 15.3% (PN, 10%; NOI, 3.3%; OI, 2%). Infections were the reason for the permanent discontinuation of ibrutinib in 9% of patients. Patients who experienced pneumonia or a severe infection showed a significantly inferior survival than those who were infection-free (p < 0.0001). A scoring system based on the three factors associated with a significant and independent impact on infections—PN or severe infection in the year before starting ibrutinib, chronic obstructive pulmonary disease, ≥2 prior treatments—identified patients with a two-to threefold increase in the rate of infections. In conclusion, the results of this study highlight the adverse impact of infectious events on the outcomes of CLL patients treated with ibrutinib.
KW - Chronic lymphocytic leukemia
KW - Ibrutinib
KW - Infection
KW - Prognosis
KW - Chronic lymphocytic leukemia
KW - Ibrutinib
KW - Infection
KW - Prognosis
UR - http://hdl.handle.net/10807/184842
U2 - 10.3390/cancers13133240
DO - 10.3390/cancers13133240
M3 - Article
SN - 2072-6694
VL - 13
SP - 3240-N/A
JO - Cancers
JF - Cancers
ER -