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:B-Cell Maturation Antigen-Directed Immunotherapies for the Treatment of Relapsed/Refractory Multiple Myeloma: A Review of the Literature and Implications for Clinical Practice.
B-Cell Maturation Antigen-Directed Immunotherapies for the Treatment of Relapsed/Refractory Multiple Myeloma: A Review of the Literature and Implications for Clinical Practice.
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靶向 BCMA 的免疫疗法是复发/难治性多发性骨髓瘤管理中的一项重要进展,并显著增加了该疾病的可用治疗选择。
综述靶向 B 细胞成熟抗原(BCMA)的免疫疗法在复发/难治性多发性骨髓瘤(RRMM)管理中的药理学、疗效、安全性、给药方案及其与患者照护和临床实践的相关性,包括CAR-T 细胞治疗和双特异性抗体(BsAb)。数据来源:检索 PubMed 1966 年至 2024 年 7 月的文献,关键词包括 idecabtagene vicleucel、ciltacabtagene autoleucel、teclistamab、elranatamab 和 multiple myeloma。另收集未发表的会议摘要和处方资料。研究筛选与数据提取:回顾所有关于抗 BCMA 免疫疗法治疗 RRMM 的相关已发表文章、未发表摘要和处方信息。数据综合:在 KarMMa-3 和 CARTITUDE-4 III 期试验中,idecabtagene vicleucel 和 ciltacabtagene autoleucel 这两种 BCMA 靶向 CAR-T 疗法分别与 MM 早期复发时的标准治疗(SOC)方案进行了比较。两项研究均显示,与 SOC 相比,缓解率、缓解深度和无进展生存期显著改善。双特异性抗体 teclistamab 和 elranatamab 分别在 MajesTEC-1 和 MagnetisMM-3 II 期试验中接受评估;在经过多线治疗的 RRMM 患者群体中,teclistamab 和 elranatamab 的总缓解率分别为 63% 和 61%。患者照护与临床实践相关性及与现有药物的比较:BCMA 靶向免疫疗法治疗 RRMM 已显示疗效。相关安全性问题包括细胞因子释放综合征、神经毒性、感染和血细胞减少。此类治疗还存在操作层面挑战及医疗可及性问题,因为它们可能仅能在具备安全给药和监测毒性基础设施的医疗机构开展。
BCMA 靶向免疫疗法是 RRMM 管理的重要进展,显著增加了该疾病的可用治疗选择。
To review the pharmacology, efficacy, safety, dosing and administration, and relevance to patient care and clinical practice of B-cell maturation antigen (BCMA) directed immunotherapies, including chimeric antigen receptor T-cell (CAR-T) therapy and bispecific antibodies (BsAb), for the management of relapsed/refractory multiple myeloma (RRMM). DATA SOURCES: A literature review of PubMed (1966 to July 2024) was conducted using the keywords idecabtagene vicleucel , ciltacabtagene autoleucel, teclistamab, elranatamab , and multiple myeloma . Data was also obtained from unpublished meeting abstracts and prescribing information. STUDY SELECTION AND DATA EXTRACTION: All relevant published articles, unpublished abstracts, and prescribing information on anti-BCMA immunotherapies for the treatment of RRMM were reviewed. DATA SYNTHESIS: Idecabtagene vicleucel and ciltacabtagene autoleucel are BCMA-directed CAR-T cell therapies that have been compared to standard of care (SOC) regimens for MM in early relapse in the phase III trials KarMMa-3 and CARTITUDE-4, respectively. Both studies demonstrated a significantly improved in response rates, depth of response, and progression-free survival compared to SOC. BsAbs teclistamab and elranatamab have been evaluated in the phase II trials MajesTEC-1 and MagnetisMM-3, respectively. Overall response rates of 63 and 61% were observed with teclistamab and elranatamab, respectively, in a population of patients with heavily pretreated RRMM.Relevance to Patient Care and Clinical Practice in Comparison with Existing Drugs:BCMA-directed immunotherapies have demonstrated efficacy in the treatment of RRMM. Safety issues with BCMA-directed immunotherapies include cytokine release syndrome, neurotoxicity, infections, and cytopenias. Operational challenges and issues with access to care exist with these therapies as they may be limited to institutions with the infrastructure to safely administer and monitor patients for toxicities.
BCMA-directed immunotherapies represent an important advancement in the management of RRMM and have significantly added to the available treatment options for this disease.
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