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:Relapsed/Refractory Multiple Myeloma: A Review of Available Therapies and Clinical Scenarios Encountered in Myeloma Relapse.
Relapsed/Refractory Multiple Myeloma: A Review of Available Therapies and Clinical Scenarios Encountered in Myeloma Relapse.
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多发性骨髓瘤仍是一种无法治愈的疾病,通常需要接受诱导治疗;符合条件者接受自体干细胞移植,并进行长期维持治疗。风险分层工具和细胞遗传学改变有助于制定个体化治疗选择,以期在维持生活质量的同时获得长期缓解。遗憾的是,由于疾病具有生物学异质性,患者可能在病程不同阶段复发。复发后的处理复杂且具有挑战性,需综合考虑治疗相关和患者相关因素。本综述广泛梳理复发/难治性多发性骨髓瘤(RRMM)的现有疗法,介绍免疫调节药物(IMiD)、蛋白酶体抑制剂(PI)、单克隆抗体(mAb)、传统化疗和venetoclax等活性疗法的药理机制。随后根据药物耐药/难治情况及自体干细胞移植(ASCT)的作用,回顾支持使用这些疗法的临床数据。综述也涉及复发期间肾功能受损和髓外病变等特殊情况的治疗方法。
最后,简要回顾支持CAR-T 细胞疗法、双特异性T细胞衔接器(BiTE)及Cereblon E3连接酶调节剂(CELMoD)应用的临床数据,展望未来。
Multiple myeloma remains an incurable disease with the usual disease course requiring induction therapy, autologous stem cell transplantation for eligible patients, and long-term maintenance. Risk stratification tools and cytogenetic alterations help inform individualized therapeutic choices for patients in hopes of achieving long-term remissions with preserved quality of life. Unfortunately, relapses occur at different stages of the course of the disease owing to the biological heterogeneity of the disease.
Addressing relapse can be complex and challenging as there are both therapy- and patient-related factors to consider. In this broad scoping review of available therapies in relapsed/refractory multiple myeloma (RRMM), we cover the pharmacologic mechanisms underlying active therapies such as immunomodulatory agents (IMiDs), proteasome inhibitors (PIs), monoclonal antibodies (mAbs), traditional chemotherapy, and Venetoclax.
We then review the clinical data supporting the use of these therapies, organized based on drug resistance/refractoriness, and the role of autologous stem cell transplant (ASCT). Approaches to special situations during relapse such as renal impairment and extramedullary disease are also covered. Lastly, we look towards the future by briefly reviewing the clinical data supporting the use of chimeric antigen receptor (CAR-T) therapy, bispecific T cell engagers (BITE), and Cereblon E3 Ligase Modulators (CELMoDs).
在 PubMed 查看 → 出版商原文(DOI) 全文 PDF(PMC)· 可下载 治疗专题与资料阅读指南 资料来源与翻译说明 报告译文或资料问题 →
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