Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Observational Study
. 2021 Apr;193(2):316-324.
doi: 10.1111/bjh.17145. Epub 2020 Oct 15.

Infections in patients with lymphoproliferative diseases treated with targeted agents: SEIFEM multicentric retrospective study

Affiliations
Observational Study

Infections in patients with lymphoproliferative diseases treated with targeted agents: SEIFEM multicentric retrospective study

Gessica Marchesini et al. Br J Haematol. 2021 Apr.

Abstract

We describe the opportunistic infections occurring in 362 patients with lymphoproliferative disorders treated with ibrutinib and idelalisib in clinical practice. Overall, 108 of 362 patients (29·8%) developed infections, for a total of 152 events. Clinically defined infections (CDI) were 49·3% (75/152) and microbiologically defined infections (MDI) were 50·7% (77/152). Among 250 patients treated with ibrutinib, 28·8% (72/250) experienced one or more infections, for a total of 104 episodes. MDI were 49% (51/104). Bacterial infections were 66·7% (34/51), viral 19·6% (10/51) and invasive fungal diseases (IFD) 13·7% (7/51). Among the 112 patients treated with idelalisib, 32·1% (36/112) experienced one or more infections, for a total of 48 episodes. MDI were 54·2% (26/48). Bacterial infections were 34·6% (9/26), viral 61·5% (16/26) and IFD 3·8% (1/26). With ibrutinib, the rate of bacterial infections was significantly higher compared to idelalisib (66·7% vs. 34·6%; P = 0·007), while viral infections were most frequent in idelalisib (61·5% vs. 19·6%; P < 0·001). Although a higher rate of IFD was observed in patients treated with ibrutinib, the difference was not statistically significant (13·7% vs. 3·8% respectively; P = 0·18). Bacteria are the most frequent infections with ibrutinib, while viruses are most frequently involved with idelalisib.

Keywords: infections; lymphoproliferative diseases; targeted therapy.

PubMed Disclaimer

Conflict of interest statement

All other authors report no potential conflict.

Figures

Fig 1
Fig 1
Cumulative incidence of infections. (A) 250 patients treated with ibrutinib of which 72 experienced infections (104 events). Median time to first infection: 148·2 days (range 3–830); (B) 112 patients treated with idelalisib of which 36 experienced infections (48 events). Median time to first infection: 175 days (range 9–690). [Colour figure can be viewed at wileyonlinelibrary.com]
Fig 2
Fig 2
Rates and etiology of infections. (A) 104 infective episodes in 72 patients treated with ibrutinib; (B) 48 infective episodes in 36 patients treated with idelalisib. n indicates the number of infective episodes.

References

    1. Morrison VA, Rai KR, Peterson BL, Kolitz JE, Elias L, Appelbaum FR, et al. Impact of therapy With chlorambucil, fludarabine, or fludarabine plus chlorambucil on infections in patients with chronic lymphocytic leukemia: Intergroup Study Cancer and Leukemia Group B 9011. J Clin Oncol. 2001;19(16):3611–21. - PubMed
    1. Hensel M, Kornacker M, Yammeni S, Egerer G, Ho AD. Disease activity and pretreatment, rather than hypogammaglobulinaemia, are major risk factors for infectious complications in patients with chronic lymphocytic leukaemia. Br J Haematol. 2003;122(4):600–6. - PubMed
    1. Moreira J, Rabe KG, Cerhan JR, Kay NE, Wilson JW, Call TG, et al. Infectious complications among individuals with clinical monoclonal B‐cell lymphocytosis (MBL): a cohort study of newly diagnosed cases compared to controls. Leukemia. 2013;27(1):136–41. - PubMed
    1. Rogers KA, Mousa L, Zhao Q, Bhat SA, Byrd JC, El Boghdadly Z, et al. Incidence of opportunistic infections during ibrutinib treatment for B‐cell malignancies. Leukemia. 2019;33(10):2527–30. - PMC - PubMed
    1. Varughese T, Taur Y, Cohen N, Palomba ML, Seo SK, Hohl TM, et al. Serious infections in patients receiving ibrutinib for treatment of lymphoid cancer. Clin Infect Dis. 2018;67(5):687–92. - PMC - PubMed

Publication types

MeSH terms