Talbot Alexis, Debureaux Pierre-Edouard, Lillo-Le Louet Agnès, Derri Yasmine, Aroux-Pavard Marine, Jantzem Hélène, Smadja David M, Touzeau Cyrille, Le Beller Christine, Gendron Nicolas
Immuno-Hematology Department, Saint-Louis Hospital, Assistance Publique Hôpitaux de Paris, Université Paris Cité, 1 Avenue Claude Vellefaux, Paris 75010, France.
Immuno-Hematology Department, Saint-Louis Hospital, Assistance Publique Hôpitaux de Paris, Université Paris Cité, Paris, France.
Ther Adv Hematol. 2025 Jul 29;16:20406207251343116. doi: 10.1177/20406207251343116. eCollection 2025.
Venetoclax is the first representative of a new class of targeted therapy, that inhibits selectively B-cell lymphoma-2 (BCL-2), an anti-apoptotic protein, frequently overexpressed in hematological malignancies. Venetoclax was approved by the Food and Drug Administration for chronic lymphocytic leukemia and for acute myeloid leukemia in 2016 and 2021, respectively. Because of its promising role in many hematological malignancies, several clinical trials are in progress and other extensions of indication are expected. An analysis of its long-term safety profile in real life is necessary.
The aim of our study was to evaluate all adverse events (AEs) reported to the French national pharmacovigilance database since its approval in France.
We performed a retrospective study of all cases of AEs occurring under venetoclax recorded in the French national pharmacovigilance database since its market approval until March 2022 in France.
During the period study, a total of 209 AEs were spontaneously reported in 123 patients, of which 173 (82%) were serious. We confirmed that the most frequent toxicities described by the summary of product characteristic (SPC) and literature data on it, including hematological (21%), gastrointestinal (11%), dermatological (9%), infectious (8%) AEs, and tumor lysis syndrome (3%). Seventy-six (36%) AEs were not listed in the SPC for which the causal relationship of venetoclax could not be excluded including autoimmune hemolytic anemias (2%) or cardiac AEs (7%).
These data especially in cardiac events provide important information on the safety of the venetoclax in a real-world setting.
维奈克拉是一类新型靶向治疗药物的首个代表药物,它可选择性抑制B细胞淋巴瘤-2(BCL-2),这是一种抗凋亡蛋白,在血液系统恶性肿瘤中经常过度表达。维奈克拉分别于2016年和2021年被美国食品药品监督管理局批准用于治疗慢性淋巴细胞白血病和急性髓系白血病。由于其在许多血液系统恶性肿瘤中具有良好前景,多项临床试验正在进行中,且有望扩大其他适应症。有必要分析其在现实生活中的长期安全性概况。
我们研究的目的是评估自维奈克拉在法国获批以来向法国国家药物警戒数据库报告的所有不良事件(AE)。
我们对法国国家药物警戒数据库中自维奈克拉在法国上市批准至2022年3月记录的所有使用维奈克拉后发生的AE病例进行了回顾性研究。
在研究期间,123例患者共自发报告了209例AE,其中173例(82%)为严重AE。我们证实,产品特性摘要(SPC)及相关文献数据中描述的最常见毒性包括血液学(21%)、胃肠道(11%)、皮肤(9%)、感染性(8%)AE以及肿瘤溶解综合征(3%)。76例(36%)AE未在SPC中列出,维奈克拉与这些AE的因果关系无法排除,包括自身免疫性溶血性贫血(2%)或心脏AE(7%)。
这些数据,尤其是心脏事件的数据,为维奈克拉在现实环境中的安全性提供了重要信息。