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:Management of relapsed refractory multiple myeloma: Evidence-based guide to community oncologists.
Management of relapsed refractory multiple myeloma: Evidence-based guide to community oncologists.
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多发性骨髓瘤(MM)是一种克隆性浆细胞恶性肿瘤,治疗具有挑战性,尤其是复发/难治性MM(RRMM)患者的治疗选择。既往接受1至3线治疗后复发通常被视为早期复发。本综述为临床医生提供早期RRMM个体化、循证治疗策略指南。文章重点介绍影响治疗选择的因素,包括患者因素(如衰弱和合并症)、疾病特征(如高危细胞遗传学)、既往治疗应答及毒性特征。
我们概述现有和新兴的变革性疗法,包括抗CD38和抗SLAMF7单克隆抗体、BCMA靶向免疫疗法(如CAR-T 细胞)以及双特异性抗体。综述总结关键临床试验的疗效(缓解率、无进展生存期、总生存期)及安全性数据(如细胞因子释放综合征、神经毒性和感染)。
重要的是,文章提供临床决策实用框架,指导不同联合方案和免疫疗法平台的选择,并讨论有意义的治疗终点及生存获益。还介绍了BCMA靶向治疗后复发管理及潜在挽救策略。未来方向包括新一代细胞疗法、新型抗体构建体、CELMoD药物以及提高免疫治疗疗效的策略。
Multiple myeloma (MM), a clonal plasma cell malignancy, presents a therapeutic challenge, especially in selecting therapy for patients with relapsed/refractory MM (RRMM). Up to 1-3 prior lines of therapy in this population are considered early relapse.
This review provides clinicians with a guide for personalized, evidence-based strategies for treatment of early RRMM. Factors influencing treatment selection, including patient-related factors (e. g. , frailty and comorbidities), disease characteristics (e. g. , high-risk cytogenetics), prior therapy response, and toxicity profiles, are highlighted.
We outline current and emerging transformative novel therapeutics, including anti-CD38 and anti-SLAMF7 monoclonal antibodies, BCMA-directed immunotherapies, such as CAR T-cells, and bispecific antibodies. The review highlights key clinical trials on efficacy (response rates, progression-free survival, overall survival) and safety profiles (e. g. , cytokine release syndrome, neurotoxicity, and infections).
Crucially, it provides a practical framework for clinical decision-making, including guidance on selecting between different combination regimens, immunotherapy platforms, and considering meaningful therapeutic endpoints and survival. Relapse management following BCMA-directed therapy and potential salvage strategies are outlined. Future directions include next-generation cellular therapies, novel antibody constructs, CELMoDs, and strategies to enhance immunotherapy outcomes.
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