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:Early evaluation of CAR-T cell therapy response in R/R DLBCL patients using (18)F-FDG PET/CT.
Early evaluation of CAR-T cell therapy response in R/R DLBCL patients using (18)F-FDG PET/CT.
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CAR-T 细胞治疗后 1 个月获得的氟-18-FDG PET/CT 结果在 R/R DLBCL 患者的早期疗效评估和进展预测中显示出准确性。
靶向CD19的CAR-T(CAR-T)细胞疗法可使复发/难治性弥漫大B细胞淋巴瘤(R/R DLBCL)患者获得持久应答。本研究评估¹⁸F-氟脱氧葡萄糖(FDG)正电子发射断层显像/计算机断层扫描(PET/CT)在接受该免疫疗法患者中的早期疗效评估价值。 对象和方法:对53例R/R DLBCL患者(男性29例、女性24例,中位年龄62岁)进行了3次独立¹⁸F-FDG PET/CT检查:桥接治疗前,即决策时点(TD);CAR-T 输注前,即输注时点(IT;tisagenlecleucel,n=37;lisocabtagene maraleucel,n=16);以及输注后1个月(M1)。基于Deauville五分量表和Lugano标准评估疗效。
IT-PET显示21例患者(39.6%)达到完全代谢缓解(CMR),其中20例维持CMR,1例在M1-PET显示进展。32例(60.4%)IT-PET未达CMR;与IT-PET相比,M1-PET分别显示12例CMR、8例部分代谢缓解(PMR)、4例无代谢缓解(NMR)和8例代谢性疾病进展(PMD)。与基线TD-PET相比,M1-PET显示32例CMR、7例PMR、5例NMR和9例PMD。中位随访10.1个月后,26例患者出现疾病进展,13例死于DLBCL。达到CMR的32例患者无进展生存期(P<0.0001)和总生存期(P<0.0001)均显著长于未达CMR的21例患者。
CAR-T 治疗后1个月进行¹⁸F-FDG PET/CT,可准确评估早期应答并预测R/R DLBCL患者疾病进展。
CD19-targeted chimeric antigen receptor T (CAR-T) cell therapy provides a durable response in patients with relapsed/refractory diffuse large B-cell lymphoma (R/R DLBCL). The role of fluorine-18-fluorodeoxyglucose ( 18 F-FDG) positron emission tomography/computed tomography (PET/CT) for early evaluation of response in patients with that immunotherapy was evaluated. SUBJECTS AND METHODS: Three separate 18 F-FDG PET/CT examinations of 53 patients (29 males, 24 females; median 62 years old) with R/R DLBCL were conducted; before bridging therapy [time of decision (TD)], before CAR-T (tisagenlecleucel, n=37; lisocabtagenemaraleucel, n=16) infusion [time of CAR-T infusion (IT)], and one month (M1) after CAR-T infusion. Response was evaluated based on the Deauville 5-point scale and Lugano criteria.
Among 21 patients (39.6%) with complete metabolic response (CMR) at IT-PET, 20 were able to continue CMR, while one showed progression at M1-PET. Among 32 patients (60.4%) with non-CMR at IT-PET, 12, 8, 4, and 8 showed CMR, partial metabolic response (PMR), (non-metabolic response (NMR), and progressive metabolic disease (PMD), respectively, at M1-PET as compared with IT-PET. Evaluations of M1-PET as compared with baseline TD-PET indicated 32, 7, 5, and 9 patients with CMR, PMR, NMR, and PMD, respectively. After a median 10.1 months, 26 patients showed progression and 13 had died from DLBCL. The 32 who achieved CMR showed significantly longer progression-free (P<0.0001) and overall survival (P<0.0001) periods as compared to the 21 non-CMR patients.
Fluorine-18-FDG PET/CT findings obtained one month after CAR-T cell therapy showed accuracy for early response evaluation and prediction of progression in patients with R/R DLBCL.
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