不适合移植的大 B 细胞淋巴瘤二线使用 axicabtagene ciloleucel:ALYCANTE 最终分析
Second-line axicabtagene ciloleucel in large B-cell lymphoma ineligible for transplantation: ALYCANTE final analysis.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Disease-specific outcomes after chimeric antigen receptor T-cell therapy.
Disease-specific outcomes after chimeric antigen receptor T-cell therapy.
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我们比较了在临床试验中接受相同CD19嵌合抗原受体(CAR)T细胞治疗的不同适应症B细胞恶性肿瘤患者的结局,包括B细胞急性淋巴细胞白血病(B-ALL)、弥漫性大B细胞淋巴瘤(DLBCL)、套细胞淋巴瘤(MCL)和滤泡性淋巴瘤(FL)。我们发现,对于同一种CAR-T 细胞,疗效和毒性因疾病而异。总体而言,我们发现与DLBCL相比,FL、MCL和B-ALL中的原发性耐药率较低。与更具侵袭性的疾病(如B-ALL、DLBCL和MCL)相比,FL中的急性毒性(细胞因子释放综合征和ICANS)似乎显著较轻。这些观察结果表明,每种B细胞恶性肿瘤都具有特定的生物学特征,其与CAR-T 细胞治疗的相互作用可能不同。因此,CAR-T 细胞可能需要根据B细胞恶性肿瘤的类型进行不同的定制,以优化其疗效和安全性。
We compared outcomes of patients with B-cell malignancies treated in clinical trials with the same CD19 chimeric antigen receptor (CAR) T-cells across different indications, including B-cell acute lymphoblastic leukaemia (B-ALL), diffuse large B-cell lymphoma (DLBCL), mantle cell lymphoma (MCL) and follicular lymphoma (FL).
We found that for a given CAR T-cell, efficacy and toxicity varied depending on the disease.
Overall, we found a low rate of primary resistance in FL, MCL and B-ALL compared with DLBCL. Acute toxicities (cytokine release syndrome and ICANS) appeared to be significantly less severe in FL compared with more aggressive diseases, such as B-ALL, DLBCL and MCL. These observations suggest that each B-cell malignancy harbours specific biology, which may interact differently with CAR T-cell therapy.
Thus, CAR T-cells may be tailored differently depending on the type of B-cell malignancy to optimise their efficacy and safety.
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