دورية أكاديمية

Bruton's tyrosine kinase inhibitor-related cardiotoxicity: The quest for predictive biomarkers and improved risk stratification.

التفاصيل البيبلوغرافية
العنوان: Bruton's tyrosine kinase inhibitor-related cardiotoxicity: The quest for predictive biomarkers and improved risk stratification.
المؤلفون: Patel JN; Department of Cancer Pharmacology and Pharmacogenomics, Atrium Health Levine Cancer Institute, Charlotte, NC 28204, USA.; Atrium Health Wake Forest Baptist Comprehensive Cancer Center, Winston-Salem, NC 27157, USA., Singh J; Sanger Heart and Vascular Institute, Atrium Health, Charlotte, NC 28204, USA., Ghosh N; Atrium Health Wake Forest Baptist Comprehensive Cancer Center, Winston-Salem, NC 27157, USA.; Department of Hematologic Malignancies and Blood Disorders, Atrium Health Levine Cancer Institute, Charlotte, NC 28204, USA.
المصدر: Oncotarget [Oncotarget] 2024 Jun 03; Vol. 15, pp. 355-359. Date of Electronic Publication: 2024 Jun 03.
نوع المنشور: Journal Article; Review
اللغة: English
بيانات الدورية: Publisher: Impact Journals Country of Publication: United States NLM ID: 101532965 Publication Model: Electronic Cited Medium: Internet ISSN: 1949-2553 (Electronic) Linking ISSN: 19492553 NLM ISO Abbreviation: Oncotarget Subsets: MEDLINE
أسماء مطبوعة: Original Publication: Albany, N.Y. : Impact Journals
مواضيع طبية MeSH: Agammaglobulinaemia Tyrosine Kinase*/antagonists & inhibitors , Agammaglobulinaemia Tyrosine Kinase*/genetics , Protein Kinase Inhibitors*/adverse effects , Cardiotoxicity*/etiology , Leukemia, Lymphocytic, Chronic, B-Cell*/drug therapy , Leukemia, Lymphocytic, Chronic, B-Cell*/genetics , Piperidines*/adverse effects , Piperidines*/therapeutic use, Humans ; Adenine/analogs & derivatives ; Adenine/adverse effects ; Risk Assessment ; Pyrimidines/adverse effects ; Pyrazoles/adverse effects ; Biomarkers ; Polymorphism, Single Nucleotide ; KCNQ1 Potassium Channel/genetics ; Tyrosine Kinase Inhibitors
مستخلص: Ibrutinib was the first Bruton's tyrosine kinase (BTK) inhibitor approved for the treatment of patients with chronic lymphocytic leukemia (CLL). While producing durable responses and prolonging survival, roughly 20-25% of patients experience dose limiting side effects, mostly consisting of cardiovascular toxicities like severe hypertension and atrial fibrillation. While clinical predictors of BTK inhibitor-related cardiotoxicity have been proposed and may aid in risk stratification, there is no routine risk model used in clinical practice today to identify patients at highest risk. A recent study investigating genetic predictors of ibrutinib-related cardiotoxicity found that single nucleotide polymorphisms in KCNQ1 and GATA4 were significantly associated with cardiotoxic events. If replicated in larger studies, these biomarkers may improve risk stratification in combination with clinical factors. A clinicogenomic risk model may aid in identifying patients at highest risk of developing BTK inhibitor-related cardiotoxicity in which further risk mitigation strategies may be explored.
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فهرسة مساهمة: Keywords: BTK inhibitor; biomarkers; cardiotoxicity; genetics; risk
المشرفين على المادة: EC 2.7.10.2 (Agammaglobulinaemia Tyrosine Kinase)
0 (Protein Kinase Inhibitors)
1X70OSD4VX (ibrutinib)
0 (Piperidines)
JAC85A2161 (Adenine)
0 (Pyrimidines)
0 (Pyrazoles)
EC 2.7.10.2 (BTK protein, human)
0 (Biomarkers)
0 (KCNQ1 Potassium Channel)
0 (Tyrosine Kinase Inhibitors)
تواريخ الأحداث: Date Created: 20240603 Date Completed: 20240603 Latest Revision: 20240605
رمز التحديث: 20240605
مُعرف محوري في PubMed: PMC11146632
DOI: 10.18632/oncotarget.28589
PMID: 38829647
قاعدة البيانات: MEDLINE
الوصف
تدمد:1949-2553
DOI:10.18632/oncotarget.28589