使用 18F-FDG PET/CT 对 R/R DLBCL 患者的 CAR-T 细胞疗法反应进行早期评估。

IF 0.9 4区 医学 Q4 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING
Kazuhiro Kitajima, Hiroyuki Yokoyama, Reona Wada, Yukihisa Tamaki, K. Yoshihara, K. Kaida, Satoshi Yoshihara, K. Yamakado
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The role of fluorine-18-fluorodeoxyglucose (18F-FDG) positron emission tomography/computed tomography (PET/CT) for early evaluation of responsein patients with that immunotherapy was evaluated.\n\n\nSUBJECTS AND METHODS\nThree separate 18F-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.\n\n\nRESULTS\nAmong 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. 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引用次数: 0

摘要

目的ECD19靶向嵌合抗原受体T(CAR-T)细胞疗法可为复发/难治性弥漫大B细胞淋巴瘤(R/R DLBCL)患者提供持久的应答。研究评估了氟-18-氟脱氧葡萄糖(18F-FDG)正电子发射断层扫描/计算机断层扫描(PET/CT)在早期评估该免疫疗法患者反应方面的作用。受试者和方法对 53 名 R/R DLBCL 患者(29 名男性,24 名女性;中位年龄 62 岁)分别进行了三次 18F-FDG PET/CT 检查;桥接治疗前[决定时间(TD)]、CAR-T(tisagenlecleucel,n=37;lisocabtagenemaraleucel,n=16)输注前[CAR-T 输注时间(IT)]和 CAR-T 输注后一个月(M1)。结果21名患者(39.6%)在IT-PET时获得完全代谢反应(CMR),20名患者能够继续CMR,1名患者在M1-PET时出现进展。在 32 名在 IT-PET 中未出现 CMR 的患者(60.4%)中,与 IT-PET 相比,在 M1-PET 中分别有 12 人、8 人、4 人和 8 人出现 CMR、部分代谢反应(PMR)、非代谢反应(NMR)和进展性代谢疾病(PMD)。与基线 TD-PET 相比,M1-PET 的评估结果显示,CMR、PMR、NMR 和 PMD 患者分别为 32 人、7 人、5 人和 9 人。在中位 10.1 个月后,26 名患者的病情出现进展,13 名患者死于 DLBCL。结论CAR-T细胞治疗一个月后获得的氟-18-FDG PET/CT结果显示,对R/R DLBCL患者的早期反应评估和进展预测具有准确性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Early evaluation of CAR-T cell therapy response in R/R DLBCL patients using 18F-FDG PET/CT.
OBJECTIVE 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 (18F-FDG) positron emission tomography/computed tomography (PET/CT) for early evaluation of responsein patients with that immunotherapy was evaluated. SUBJECTS AND METHODS Three separate 18F-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. RESULTS 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. CONCLUSION 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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来源期刊
CiteScore
1.40
自引率
6.70%
发文量
34
审稿时长
>12 weeks
期刊介绍: The Hellenic Journal of Nuclear Medicine published by the Hellenic Society of Nuclear Medicine in Thessaloniki, aims to contribute to research, to education and cover the scientific and professional interests of physicians, in the field of nuclear medicine and in medicine in general. The journal may publish papers of nuclear medicine and also papers that refer to related subjects as dosimetry, computer science, targeting of gene expression, radioimmunoassay, radiation protection, biology, cell trafficking, related historical brief reviews and other related subjects. Original papers are preferred. The journal may after special agreement publish supplements covering important subjects, dully reviewed and subscripted separately.
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