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:The treatment landscape for Relapsed Refractory B Acute Lymphoblastic Leukaemia (ALL).
The treatment landscape for Relapsed Refractory B Acute Lymphoblastic Leukaemia (ALL).
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。
过去八年,复发难治性(RR)急性淋巴细胞白血病(ALL)患者的挽救治疗选择迅速扩展。blinatumomab 和 Inotuzumab ozogamicin(InO)等靶向方法的疗效优于传统化疗方案,且毒性降低也转化为更高的移植实现率。影响这两种抗体序贯使用的因素包括:对于高疾病负荷患者优先选择 InO,而 blinatumomab 是在低疾病负荷组中获得 MRD 缓解的更优药物。对于有明显肝病的患者,不应首先使用 InO。最令人瞩目的是嵌合抗原受体细胞疗法(CAR-T)的出现,它使相当一部分年轻 RR-ALL 患者获得治愈性治疗。目前在选择复发治疗时需要仔细考虑;本综述总结了当前可用的策略以及如何 navigate RR ALL 的治疗格局。
The last eight years have seen a rapid expansion of salvage options for patients with relapsed refractory (RR) acute lymphoblastic leukemia (ALL). The efficacy of targeted approaches with blinatumomab and Inotuzumab ozogamicin (InO), outweigh that of conventional chemotherapeutic regimens, and the reduced toxicity profile has also translated into higher transplant realization rates. Factors influencing the sequential use of these two antibodies include the preference for InO in those with high disease burden, while blinatumomab is a superior agent for attaining MRD responses in low disease burden groups.
InO should not be used first in those with significant liver disease. Most impressive is the advent of chimeric antigen receptor cell therapy (CAR-T), a curative therapy in a significant proportion of younger patients with RR-ALL. Careful consideration is now required in the selection of relapse therapies; this review summarizes current available strategies and how to navigate the treatment landscape for RR ALL.
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