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:Next-generation immunotherapy in relapsed/refractory multiple myeloma: Strategies to achieve sustained MRD negativity.
Next-generation immunotherapy in relapsed/refractory multiple myeloma: Strategies to achieve sustained MRD negativity.
分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。
本研究批判性审视多发性骨髓瘤(MM)治疗格局的演变,重点关注转向免疫治疗策略以对抗这一复杂血液系统恶性肿瘤。尽管 MM 面临复发率和进展率高等临床挑战,近期治疗创新已开启新的治疗可能。蛋白酶体抑制剂和免疫调节药物的出现,以及近年 BCMA 靶向免疫疗法(如 CAR-T 和双特异性抗体)的发展,拓宽了 MM 治疗选择。这些疗法有望实现持续微小残留病(MRD)阴性并改善患者结局。为应对传统疗法的局限,本综述强调迫切需要能够带来持久应答并克服疾病固有治疗耐药的新型治疗模式。分析进一步探讨免疫疗法,尤其是复发/难治性 MM 患者的治疗作用,同时承认治疗耐药、副作用和治疗可及性方面仍存在挑战。此外,作者倡导将免疫疗法纳入更早期治疗方案,并强调先进疗法全球可及的重要性。通过这一探讨,综述旨在促进血液病学领域持续讨论和研究,优化 MM 治疗策略、改善患者结局,并推进最终治愈 MM 的目标。
This study critically examines the evolving landscape of Multiple Myeloma (MM) treatment, spotlighting the shift towards immunotherapeutic strategies in combating this complex hematological malignancy. Despite the clinical challenges posed by MM, including its high relapse and progression rates, recent therapeutic innovations have ushered in a new era of treatment possibilities. The advent of proteasome inhibitors and immunomodulatory drugs, and more recently BCMA targeted immunotherapies such as CAR T cells and bispecific antibodies, has broadened therapeutic options in multiple myeloma.
These modalities show significant potential to achieve sustained minimal residual disease (MRD) negativity and improve patient outcomes. Addressing the limitations of conventional therapies, this review highlights the critical need for novel treatment modalities that can provide durable responses and overcome the disease's inherent resistance to treatment.
The analysis further explores the impact of immunotherapeutic approaches, particularly for patients with relapsed or refractory MM, while acknowledging the ongoing challenges related to treatment resistance, side effects, and therapy accessibility.
Additionally, it advocates for the integration of immunotherapy into earlier treatment protocols and emphasizes the importance of global accessibility to these advanced treatments. Through this exploration, the review aims to contribute to the hematological community's ongoing dialogue and research efforts, striving to refine MM treatment strategies, enhance patient outcomes, and advance towards the ultimate goal of finding a cure for MM.
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