CAR-T(CAR-T)细胞疗法在非肿瘤性疾病中的应用
Chimeric antigen receptor T (CAR-T) cell therapy in non-oncological diseases.
CAR-T(CAR-T)细胞在血液系统恶性肿瘤中的应用推动了这种免疫治疗形式的显著进展。
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Update on Thrombosis Risk in Patients with Cancer: Focus on Novel Anticancer Immunotherapies.
Update on Thrombosis Risk in Patients with Cancer: Focus on Novel Anticancer Immunotherapies.
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血栓栓塞并发症,包括静脉血栓栓塞症(VTE)和动脉血栓栓塞症(ATE),会增加癌症患者的死亡率和发病率,并延误治疗。因此,需要更深入地了解潜在的風險特征,识别风险因素和预测性生物标志物,并最终为癌症患者制定特定的心血管预防策略。近年来,随着靶向治疗和免疫治疗选择(包括免疫检查点抑制剂(ICI)、嵌合抗原受体(CAR)T细胞疗法和双特异性T细胞衔接器(BiTEs))的出现,医学抗癌治疗取得了显著进展。这些进展对癌症患者伴随的血栓栓塞事件风险具有重要影响。首先,这些高效疗法的使用增加,使得尽管处于晚期癌症阶段但患者生存期延长,从而导致越来越大比例的癌症患者面临长期血栓栓塞事件风险。其次,新型抗癌免疫疗法潜在的直接心血管毒性和促血栓形成效应是持续争论的话题,新出现的报告提示与ICI相关的VTE和ATE风险,以及与BiTEs和CAR-T 细胞疗法相关的常见细胞因子释放综合征中出现的相关止血功能失调。本叙述性综述旨在总结抗癌免疫疗法的兴起对癌症患者血栓栓塞事件的影响,并概述与ICI、CAR-T 细胞疗法和BiTEs相关的VTE和ATE发生率及风险因素的现有数据。
Thromboembolic complications, including venous thromboembolism (VTE) and arterial thromboembolism (ATE), increase mortality and morbidity, and delay treatment in patients with cancer.
Therefore, an increased understanding of underlying risk profiles, the identification of risk factors and predictive biomarkers, and ultimately the development of specific cardiovascular prevention strategies in patients with cancer is needed. Medical anticancer therapies have undergone a remarkable development in recent years with the advent of targeted and immunotherapeutic treatment options, including immune checkpoint inhibitors (ICI), chimeric antigen receptor (CAR) T-cell therapies and bispecific T-cell engagers (BiTEs). These developments have important implications for the accompanied risk of thromboembolic events in patients with cancer. First, the increased use of these highly effective therapies renders a growing proportion of patients with cancer at risk of thromboembolic events for a prolonged risk period due to an increase in patient survival despite advanced cancer stages.
Second, potential direct cardiovascular toxicity and prothrombotic effect of novel anticancer immunotherapies are a matter of ongoing debate, with emerging reports suggesting a relevant risk of VTE and ATE associated with ICI, and relevant dysregulations of hemostasis in the frequently observed cytokine-release syndrome associated with BiTEs and CAR T-cell therapy.
The aim of the present narrative review is to summarize the implications of the emerging use of anticancer immunotherapy for thromboembolic events in patients with cancer, and to provide an overview of available data on the rates and risk factors for VTE and ATE associated with ICI, CAR T-cell therapy, and BiTEs.
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