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:Efficacy and side effects of anti-CD19 CAR T-cell therapy in patients with relapsed/refractory gastrointestinal lymphoma.
Efficacy and side effects of anti-CD19 CAR T-cell therapy in patients with relapsed/refractory gastrointestinal lymphoma.
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高肿瘤负荷、胃肠道受累、肿块或结节型及胃肠道出血组的 ORR 和 CR 较低。胃肠道病变组和胃肠道出血组的 CRS 分级较高。仅胃肠道受累的患者发生胃肠道出血的风险较高。
尽管抗CD19嵌合抗原受体(CAR)T细胞疗法已被批准作为复发/难治性(R/R)B细胞淋巴瘤非常有效的挽救策略,但在R/R胃肠道(GI)淋巴瘤中的经验仍然不足。
我们总结了抗CD19 CAR-T 细胞疗法在12例R/R GI淋巴瘤患者中的疗效和副作用。基于文献,将R/R GI淋巴瘤患者按不同特征分为亚组:大包块/无大包块疾病、胃/胃肠道受累、胃肠道/合并胃肠道外病变、溃疡/肿块或结节型、有/无胃肠道出血。
这12例患者的客观缓解率(ORR)为66.67%。无大包块病组ORR为83.33%,胃受累组为80.00%,溃疡型组为100.00%,无消化道出血组为80.00%。这12例患者的CR率为33.33%。无大包块病组CR为50.0%,胃受累组为60.00%,溃疡型组为80.00%。这12例患者输注后6个月的PFS和OS率分别为54.55%和58.33%。无大包块病组6个月的总生存期(OS)更高。其他各组之间6个月的OS或无进展生存期(PFS)无差异。消化道病变组CAR-T 细胞平均峰值和细胞因子释放综合征(CRS)分级更高。消化道出血组IFN-平均峰值和CRS分级更高。消化道病变组6例患者中有4例为高肿瘤负荷患者。仅消化道受累的患者发生消化道出血的风险更高。
We summarized the efficacy and side effects of anti-CD19 CAR T-cell therapy in 12 patients with R/R GI lymphoma. Based on literature, the R/R GI lymphoma patients were divided into subgroups with different characteristics: Bulky/No bulky disease, Gastric/Gastrointestinal involvement, Gastrointestinal/Combined extra-gastrointestinal lesions, Ulcer/Lumps or nodules type, With/without gastrointestinal bleeding.
The objective response rate (ORR) was 66.67% in these 12 patients. The ORR was 83.33% in no bulky disease group, 80.00% in gastric involvement group, 100.00% in ulcer type group, and 80.00% in no gastrointestinal bleeding group. The CR rate was 33.33% in these 12 patients. The CR was 50.0% in no bulky disease group, 60.00% in gastric involvement group, and 80.00% in ulcer type group. The PFS and OS rate of the 12 patients at 6 months after infusion were 54.55% and 58.33%, respectively. The overall survival (OS) at 6 months was higher in no bulky disease group. There was no difference of the OS or the progression free survival (PFS) at 6 months between the other groups. The mean peak of CAR-T cells and Cytokine Release Syndrome (CRS) grade were higher in gastrointestinal lesions group. The mean peak of IFN- and CRS grade were higher in gastrointestinal bleeding group. Four out of six patients in group of gastrointestinal lesions group were patient with high tumor burden. Patients with gastrointestinal involvement only were at higher risk for gastrointestinal bleeding.
The ORR and CR of high tumor load, gastrointestinal involvement, lumps or nodules type and gastrointestinal bleeding group were lower. The CRS grade was higher in gastrointestinal lesions group and in gastrointestinal bleeding group. Patients with gastrointestinal involvement only were at higher risk for gastrointestinal bleeding.
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