Invasive fungal infection incidence and risk factors in patients receiving ibrutinib in real-life settings: A nationwide population-based cohort study

被引:4
作者
Allouchery, Marion [1 ,2 ,3 ]
Brunet, Kevin [2 ,4 ,5 ]
Tomowiak, Cecile [6 ,7 ]
Singier, Allison [3 ]
Pambrun, Elodie [3 ]
Pariente, Antoine [3 ]
Bezin, Julien [3 ,8 ]
Perault-Pochat, Marie-Christine [1 ,9 ]
Salvo, Francesco [3 ,8 ]
机构
[1] CHU Poitiers, Pharmacol Clin & Vigilances, 2 Rue Miletrie, F-86021 Poitiers, France
[2] Univ Poitiers, Fac Med & Pharm, Poitiers, France
[3] Univ Bordeaux, INSERM, BPH, Team AHeaD,U1219, Bordeaux, France
[4] Univ Poitiers, Inserm U1070 PHAR2, Poitiers, France
[5] CHU Poitiers, Lab Parasitol & Mycol Med, Poitiers, France
[6] CHU Poitiers, Oncohematol & Therapie Cellulaire, Poitiers, France
[7] CHU Poitiers, INSERM CIC 1402, Poitiers, France
[8] CHU Bordeaux, Serv Informat Med, Pole Sante Publ, Bordeaux, France
[9] Univ Poitiers, Lab Neurosci Expt & Clin, INSERM, UMR1084, Poitiers, France
关键词
ibrutinib; invasive fungal infection; observational study; chronic lymphocytic leukaemia; non-Hodgkin lymphoma; Waldenstrom macroglobulinaemia; BRUTON TYROSINE KINASE; CHRONIC LYMPHOCYTIC-LEUKEMIA; FRANCE; DISEASE; SNIIRAM;
D O I
10.1111/myc.13676
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Background: Data on the risk of invasive fungal infections (IFI) with ibrutinib treatment are scarce.Objectives: This study aimed to determine IFI incidence and risk factors in ibrutinib-treated patients in real-life settings.Methods: We constituted a cohort of ibrutinib incident users in the French National Healthcare Database. All patients >= 18 years with a first dispensing of ibrutinib between 21 November 2014 and 31 December 2019 were included. Patients were followed from the cohort entry date until IFI, ibrutinib discontinuation, death, or 31 December 2020, whichever came first. The cumulative incidence function method was used to estimate the probability of IFI accounting for competing risk of death. A multivariate cause-specific Cox proportional hazards model was used to assess independent IFI risk factors.Results: Among 6937 ibrutinib-treated patients, 1-year IFI cumulative incidence was 1.3%, with invasive aspergillosis being the most frequent. Allogenic or autologous stem cell transplantation (ASCT) (hazard ratio [HR] 3.59, 95% confidence interval [1.74; 7.41]), previous anticancer treatment (HR 2.12, CI 95% [1.34; 3.35]) and chronic respiratory disease (HR 1.66, [1.03; 2.67]) were associated with higher risk of IFI. Besides neutropenia and corticosteroids, use of anti-CD20 agents was significantly more frequent in patients having experienced IFI (HR 3.68, [1.82; 7.45]).Conclusions: In addition to patients with ASCT history, severe neutropenia or treated with corticosteroids, our findings support active surveillance of IFIs in those with chronic respiratory disease, previously treated, or treated with anti-CD20 agents in combination with ibrutinib. Further studies are needed to optimise IFI prophylaxis in these patient subgroups.
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页数:8
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