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.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Management of Primary Refractory Diffuse Large B-Cell Lymphoma in Patients Unsuitable for CAR T-Cell Therapy.
Management of Primary Refractory Diffuse Large B-Cell Lymphoma in Patients Unsuitable for CAR T-Cell Therapy.
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原发性难治性弥漫大B细胞淋巴瘤与不良结局及对常规挽救治疗反应有限相关。尽管CAR-T 细胞疗法是该情况下的标准治疗,但相当比例的患者尽管符合疾病相关标准却无法接受该治疗。在本综述中,“不适合”是指因可逆的临床状况、需要立即减瘤的快速进展性疾病或后勤和社会障碍而暂时或功能上无法接受CAR-T 细胞疗法的患者,而非永久性禁忌症。对于这些患者,需要及时的替代策略。传统的以铂类为基础或含吉西他滨和苯达莫司汀的方案在短期疾病控制中仍有一定作用,但持久性有限。相比之下,新型抗体-based疗法,包括含polatuzumab的联合方案、loncastuximab tesirine以及tafasitamab联合来那度胺,扩大了治疗选择并改善了耐受性。最值得注意的是,CD20 CD3双特异性抗体代表了一项重大治疗进展,提供了即用型免疫衔接,且主要以门诊给药为主。从实践角度来看,早期识别CAR-T 细胞疗法的可逆障碍并及时使用双特异性抗体或其他抗体-based方案,对于实现快速疾病控制、保护器官功能以及在可行时恢复细胞治疗资格至关重要。
Primary refractory Diffuse Large B-Cell Lymphoma is associated with poor outcomes and limited responsiveness to conventional salvage therapies. Although CAR T-cell therapy represents the standard of care in this setting, a substantial proportion of patients cannot receive it despite meeting disease-related criteria. In this review, "unsuitable" refers to patients who are temporarily or functionally unable to undergo CAR T-cell therapy because of reversible clinical conditions, rapidly progressive disease requiring immediate cytoreduction, or logistical and social barriers, rather than permanent contraindications. For these patients, prompt alternative strategies are required. Conventional platinum-based or gemcitabine- and bendamustine-containing regimens retain a role for short-term disease control but offer limited durability.
In contrast, novel antibody-based therapies, including polatuzumab-containing combinations, loncastuximab tesirine, and tafasitamab plus lenalidomide, have expanded treatment options with improved tolerability. Most notably, CD20 CD3 bispecific antibodies represent a major therapeutic advance, providing off-the-shelf immune engagement with predominantly outpatient administration.
From a practical perspective, early identification of reversible barriers to CAR T-cell therapy and timely use of bispecific antibodies or other antibody-based regimens are critical to achieve rapid disease control, preserve organ function, and, when feasible, restore eligibility for cellular therapy.
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