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Targeted therapies in CLL/SLL and the cumulative incidence of infection: A systematic review and meta-analysis.
Vassilopoulos, Stephanos; Shehadeh, Fadi; Kalligeros, Markos; Tran, Quynh-Lam; Schiffman, Fred; Mylonakis, Eleftherios.
Afiliação
  • Vassilopoulos S; Infectious Diseases Division, Rhode Island Hospital, Providence, RI, United States.
  • Shehadeh F; Warren Alpert Medical School of Brown University, Providence, RI, United States.
  • Kalligeros M; Infectious Diseases Division, Rhode Island Hospital, Providence, RI, United States.
  • Tran QL; Warren Alpert Medical School of Brown University, Providence, RI, United States.
  • Schiffman F; School of Electrical and Computer Engineering, National Technical University of Athens, Athens, Greece.
  • Mylonakis E; Infectious Diseases Division, Rhode Island Hospital, Providence, RI, United States.
Front Pharmacol ; 13: 989830, 2022.
Article em En | MEDLINE | ID: mdl-36188587
Background: Patients with chronic lymphocytic leukemia (CLL)/small lymphocytic lymphoma (SLL) are prone to infections. Aims: Provide a pooled estimate of the cumulative incidence for infections that fulfilled the criteria associated with severe infectious adverse events for grade 3 or higher (including pneumonia, febrile neutropenia and sepsis) in patients who receive targeted therapies. Methods: We searched PubMed and EMBASE for randomized controlled trials (RCT) that included patients with CLL/SLL who received targeted therapies and performed a random-effects meta-analysis to estimate the cumulative incidence of infections. Results: Of 2,914 studies screened, we retrieved 31 which evaluated 11,660 patients. The pooled cumulative incidence of infections for patients who received treatment regimens based on a BTK inhibitors was 19.86%. For patients who received treatment based on rituximab and second generation anti-CD20 monoclonal antibodies, the pooled cumulative incidence of infections was 19.85 and 13.46%, respectively. Regarding PI3K inhibitor-based regimens the cumulative incidence of severe infections was 30.89%. BCL-2 inhibitors had a cumulative incidence of infections of 17.49% while lenalidomide and alemtuzumab had an incidence of 13.33 and 45.09%, respectively. The cumulative incidence of pneumonia ranged from 3.01 to 8.45% while febrile neutropenia ranged from 2.68 to 10.80%. Regarding sepsis, the cumulative incidence ranged from 0.9 to 4.48%. Conclusion: Patients with CLL/SLL who receive targeted therapies may develop severe infections at significant rates that, in addition to disease stage and other complications, depend on the mechanism of action of the used drug. Surveillance for infections and development of effective prophylactic strategies are critical for patients with CLL/SLL who receive targeted therapies. Systematic Review Registration: [https://systematicreview.gov/], identifier [registration number].
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Clinical_trials / Incidence_studies / Prognostic_studies / Risk_factors_studies / Systematic_reviews Idioma: En Revista: Front Pharmacol Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Estados Unidos País de publicação: Suíça

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Clinical_trials / Incidence_studies / Prognostic_studies / Risk_factors_studies / Systematic_reviews Idioma: En Revista: Front Pharmacol Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Estados Unidos País de publicação: Suíça