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:Autoimmune cytopenias in chronic lymphocytic leukemia in the era of novel drugs.
Autoimmune cytopenias in chronic lymphocytic leukemia in the era of novel drugs.
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尽管自身免疫性血细胞减少症的治疗取得了进展,目前的管理仍主要依赖皮质类固醇治疗。支持在此情况下使用新型靶向药物的明确证据仍然有限。未来的进展取决于专门的临床试验,旨在更好地明确新兴疗法的作用并实现更个性化的治疗策略,尽管与慢性淋巴细胞白血病相关的自身免疫性血细胞减少症的罕见性构成了重大挑战。
自身免疫性血细胞减少是慢性淋巴细胞白血病的常见并发症,导致患者发病率增加和生活质量下降。随着慢性淋巴细胞白血病新型治疗药物的开发,这些并发症的诊断和管理已得到改善。涵盖领域:本综述总结了慢性淋巴细胞白血病患者自身免疫性血细胞减少的诊断和管理方面的关键发现,特别关注新型治疗药物的影响。这些药物包括Bruton酪氨酸激酶抑制剂、B细胞淋巴瘤2蛋白抑制剂、单克隆抗体和双特异性抗体、磷脂酰肌醇3-激酶抑制剂以及CAR-T 细胞疗法。本综述基于PubMed数据库检索截至2026年3月1日发表的文章,涵盖上述主题,并结合作者的临床和研究经验。
INTRODUCTION: Autoimmune cytopenias are common complications of chronic lymphocytic leukemia, leading to increased morbidity and a reduced quality of life for affected patients. The diagnosis and management of these complications have improved with the development of new therapeutic agents for chronic lymphocytic leukemia. AREAS COVERED: This review summarizes the key findings on diagnosing and managing autoimmune cytopenias in patients with chronic lymphocytic leukemia, with a particular focus on the impact of new therapeutic agents. These include Bruton tyrosine kinase inhibitors, B-cell lymphoma 2 protein inhibitors, monoclonal and bispecific antibodies, phosphatidylinositol 3-kinase inhibitors, and chimeric antigen receptor T-cell therapies.
The review is based on a PubMed database search for articles published up to March 1, 2026, covering the abovementioned topics, as well as the authors' clinical and research experience. EXPERT OPINION: Despite advances in the treatment of autoimmune cytopenias, current management still primarily relies on corticosteroid therapy.
Clear evidence supporting the use of novel targeted agents in this setting remains limited. Future progress depends on dedicated clinical trials aimed at better defining the role of emerging therapies and enabling more personalized treatment strategies, although the rarity of autoimmune cytopenias associated with chronic lymphocytic leukemia presents a significant challenge.
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