Doig Christopher, Yannakou Costas Kleanthes
Department of Molecular Oncology and Cancer Immunology, Epworth HealthCare, Melbourne, VIC, Australia.
Department of Clinical Pathology, The University of Melbourne, Parkville, VIC, Australia.
Front Med (Lausanne). 2025 Jul 2;12:1582975. doi: 10.3389/fmed.2025.1582975. eCollection 2025.
Bispecific antibodies (bsAbs) are an emerging class of directed immunotherapies with established uses in certain hematological malignancies as well as an emerging role in the treatment of solid organ malignancy. These molecules are able to juxtapose T cells (in most cases) with target tumor cells, forming an immunological synapse. bsAbs are under extensive investigation in the treatment of B-cell non-Hodgkin lymphomas, with encouraging results in both the monotherapy and combination therapy settings. In this review we summarize the key toxicities associated with the use of lymphoma-targeting bsAbs: cytokine release syndrome, immune effector cell associated neurotoxicity syndrome, cytopenias, infections and immunosuppression as well as tumor lysis syndrome. While the toxicities are not insignificant, they are typically manageable and justifiable given the unmet medical need, especially in the case of relapsed or refractory disease.
双特异性抗体(bsAbs)是一类新兴的定向免疫疗法,在某些血液系统恶性肿瘤中已确立其用途,并且在实体器官恶性肿瘤的治疗中也发挥着越来越重要的作用。这些分子能够(在大多数情况下)使T细胞与靶肿瘤细胞并列,形成免疫突触。bsAbs在B细胞非霍奇金淋巴瘤的治疗中正在进行广泛研究,在单药治疗和联合治疗中均取得了令人鼓舞的结果。在本综述中,我们总结了与使用靶向淋巴瘤的bsAbs相关的主要毒性:细胞因子释放综合征、免疫效应细胞相关神经毒性综合征、血细胞减少、感染和免疫抑制以及肿瘤溶解综合征。虽然这些毒性并非微不足道,但鉴于未满足的医疗需求,它们通常是可控的且合理的,尤其是在复发或难治性疾病的情况下。