伊布替尼
威尼斯人
医学
止血
内科学
不利影响
肿瘤科
耐受性
慢性淋巴细胞白血病
药理学
白血病
作者
Rebecca Svanberg Teglgaard,Sisse Rye Ostrowski,Kazem Nasserinejad,Sabina Kersting,Johan A. Dobber,Mattias Mattson,Hoa Tran,Mark‐David Levin,Rogier Mous,Arnon P. Kater,Carsten U. Niemann
标识
DOI:10.1080/10428194.2020.1811270
摘要
Bleeding is a common adverse event following ibrutinib monotherapy. However, it remains unclear how hemostasis is affected by venetoclax in combination with ibrutinib. Here we investigated hemostasis in patients with chronic lymphocytic leukemia (CLL) at baseline, during ibrutinib monotherapy, and during venetoclax and ibrutinib combination therapy or venetoclax monotherapy. Primary hemostasis, assessed by Multiplate using adenosine diphosphate (ADP), arachidonic acid (AA), and thrombin receptor agonist peptide (TRAP-6), was impaired in all CLL patients at baseline, remained unchanged upon ibrutinib monotherapy, and improved significantly following venetoclax added to ibrutinib or as monotherapy. Secondary hemostasis assessed by thromboelastography (TEG) was normal and unchanged throughout treatment. The frequency of clinical bleeding events was the highest during ibrutinib monotherapy, in line with the demonstrated improved primary hemostasis upon addition of venetoclax, thus pointing toward a treatment option for CLL patients with increased bleeding risk.
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