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:Future Directions in Allogeneic Stem Cell Transplantation in Acute Lymphoblastic Leukemia.
Future Directions in Allogeneic Stem Cell Transplantation in Acute Lymphoblastic Leukemia.
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ASCT 仍是高危 ALL 的关键治疗手段,在预处理方案、移植物工程和移植后策略方面取得了进展。未来的重点将放在优化患者选择、用于 CAR-T 后巩固治疗以及改进移植物处理,旨在实现 ASCT 的个性化,并提高 ALL 患者的生存率和生活质量。
异基因干细胞移植(ASCT)数十年来一直是急性淋巴细胞白血病(ALL)治疗的基石,患者生存率显著改善。这些进步与更好的疗法、精细化的预处理方案以及微小残留病监测相关。尽管取得了进展,在减少复发、治疗相关死亡率和毒性方面仍存在挑战。概述:本文探讨了ASCT治疗ALL的最新进展,重点关注预处理方案、移植物工程和移植后治疗。关键进展包括识别出哪些患者可从减低强度预处理而非清髓性预处理或降低全身照射(TBI)剂量中获益,从而改善结局并降低毒性。创新的移植物处理策略,如Orca-T和Orca-Q,旨在增强移植物抗白血病效应,同时尽量减少移植物抗宿主病(GVHD)。此外,移植后治疗,包括靶向治疗、免疫治疗和CAR-T 细胞,在预防复发方面显示出前景。错配供者使用和GVHD预防方面的进展正在拓宽供者选择并减少不良反应,提高ASCT在ALL中的安全性和有效性。
BACKGROUND: Allogeneic stem cell transplantation (ASCT) has been a cornerstone of acute lymphoblastic leukemia (ALL) treatment for decades, with significant improvements in patient survival. These advancements are linked to better therapies, refined conditioning regimens, and minimal residual disease monitoring. Despite progress, challenges remain in reducing relapse, treatment-related mortality, and toxicity. SUMMARY: This article explores recent advancements in ASCT for ALL, focusing on conditioning regimens, graft engineering, and post-transplant therapies. Key developments include identifying patients who benefit from reduced-intensity conditioning over myeloablative conditioning or reduction in dose of total body irradiation (TBI), leading to improved outcomes and lower toxicity. Innovative graft manipulation strategies, such as Orca-T and Orca-Q, aim to enhance graft-versus-leukemia effects while minimizing graft-versus-host disease (GVHD). Additionally, post-transplant therapies, including targeted treatments, immunotherapies, and CAR-T cells, are showing promise in preventing relapse. Advances in mismatched donor use and GVHD prophylaxis are broadening donor options and reducing adverse effects, improving ASCT's safety and effectiveness in ALL. KEY MESSAGES: ASCT remains a critical treatment for high-risk ALL, with advancements in conditioning, graft engineering, and post-transplant strategies. Future focus will be on optimizing patient selection, use in post-CAR-T consolidation, and refining graft manipulation, aiming to personalize ASCT and enhance survival and quality of life for ALL patients.
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