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Cardiovascular events reported in patients with B-cell malignancies treated with zanubrutinib.
Moslehi, Javid J; Furman, Richard R; Tam, Constantine S; Salem, Joe-Elie; Flowers, Christopher R; Cohen, Aileen; Zhang, Meng; Zhang, Jun; Chen, Lipeng; Ma, Han; Brown, Jennifer R.
Afiliación
  • Moslehi JJ; Section of Cardio-Oncology & Immunology, UCSF School of Medicine, San Francisco, CA.
  • Furman RR; Department of Medicine, Weill Cornell Medicine, New York, NY.
  • Tam CS; Alfred Hospital and Monash University, Melbourne, VIC, Australia.
  • Salem JE; AP-HP Sorbonne, Paris, France.
  • Flowers CR; Department of Lymphoma/Myeloma, The University of Texas MD Anderson Cancer Center, Houston, TX.
  • Cohen A; BeiGene Inc, San Mateo, CA.
  • Zhang M; BeiGene Inc, San Mateo, CA.
  • Zhang J; BeiGene Inc, San Mateo, CA.
  • Chen L; BeiGene Co, Ltd, Beijing, China.
  • Ma H; BeiGene Inc, San Mateo, CA.
  • Brown JR; Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA.
Blood Adv ; 8(10): 2478-2490, 2024 May 28.
Article en En | MEDLINE | ID: mdl-38502198
ABSTRACT
ABSTRACT First-generation Bruton tyrosine kinase (BTK) inhibitor, ibrutinib, has been associated with an increased risk of cardiovascular toxicities. Zanubrutinib is a more selective, next-generation BTK inhibitor. In this analysis, incidence rates of atrial fibrillation, symptomatic (grade ≥2) ventricular arrhythmia, and hypertension were evaluated in a pooled analysis of 10 clinical studies with zanubrutinib monotherapy in patients (N = 1550) with B-cell malignancies and a pooled analysis of head-to-head studies comparing zanubrutinib with ibrutinib (ASPEN cohort 1; ALPINE). Among the 10 studies, most patients (median age, 67 years) were male (66.3%) and had CLL/SLL (60.5%). Overall incidence and exposure-adjusted incidence rates (EAIR) for atrial fibrillation, symptomatic ventricular arrhythmia, and hypertension were lower with zanubrutinib than ibrutinib. Despite a similar prevalence of preexisting cardiovascular events in ASPEN and ALPINE, atrial fibrillation/flutter incidence rates (6.1% vs 15.6%) and EAIR (0.2 vs 0.64 persons per 100 person-months; P < .0001) were lower with zanubrutinib than with ibrutinib. Symptomatic ventricular arrhythmia incidence was low for both zanubrutinib (0.7%) and ibrutinib (1.7%) with numerically lower EAIR (0.02 vs 0.06 persons per 100 person-months, respectively) for zanubrutinib. The hypertension EAIR was lower with zanubrutinib than ibrutinib in ASPEN but similar between treatment arms in ALPINE. The higher hypertension EAIR in ALPINE was inconsistent with other zanubrutinib studies. However, fewer discontinuations (1 vs 14) and deaths (0 vs 6) due to cardiac disorders occurred with zanubrutinib versus ibrutinib in ALPINE. These data support zanubrutinib as a treatment option with improved cardiovascular tolerability compared with ibrutinib for patients with B-cell malignancies in need of BTK inhibitors. These trials were registered at www.ClinicalTrials.gov as # NCT03053440, NCT03336333, NCT03734016, NCT04170283, NCT03206918, NCT03206970, NCT03332173, NCT03846427, NCT02343120, and NCT03189524.
Asunto(s)

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Piperidinas / Pirazoles / Pirimidinas Límite: Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Blood Adv Año: 2024 Tipo del documento: Article País de afiliación: Canadá

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Piperidinas / Pirazoles / Pirimidinas Límite: Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Blood Adv Año: 2024 Tipo del documento: Article País de afiliación: Canadá