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CAR T 细胞治疗后接受 loncastuximab tesirine 治疗的复发或难治性弥漫性大 B 细胞淋巴瘤患者的结局。

Outcomes with loncastuximab tesirine following CAR T-cell therapy in patients with relapsed or refractory diffuse large B-cell lymphoma.

机构信息

Division of Hematology and Hematologic Malignancies, Huntsman Cancer Institute, University of Utah, Salt Lake City, UT, USA.

ADC Therapeutics, New Providence, NJ, USA.

出版信息

Blood Cancer J. 2024 Nov 28;14(1):210. doi: 10.1038/s41408-024-01195-4.

DOI:10.1038/s41408-024-01195-4
PMID:39609431
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11604956/
Abstract

The efficacy of loncastuximab tesirine (lonca) following chimeric antigen receptor T-cell therapy (CAR-T) progression/failure is unknown. Hence, we sought to examine real-world use and outcomes of lonca following CAR-T in patients with relapsed or refractory (R/R) diffuse large B-cell lymphoma (DLBCL) in the USA. In this retrospective study, we included adults (age ≥ 18 years) with R/R DLBCL who received lonca monotherapy as third- (3 L) or fourth line (4 L) treatment after progressing on second line (2 L) or 3 L CAR-T, respectively. Post-CAR-T lonca outcomes included response rates (overall response rate [ORR] and complete response [CR] rate), duration of response (DOR), progression-free survival (PFS), and overall survival (OS). A total of 118 patients were included in the analysis with 95 receiving lonca following 2 L CAR-T (median age:66 years; 61% male) and 23 following 3 L CAR-T (median age:57 years; 43% male). Patients with 2 L CAR-T/3 L lonca had an ORR of 73% (CR rate of 34%). With a median follow-up of 8.5 months following lonca initiation, median DOR, PFS, and OS were not reached. The DOR, PFS, and OS at 12 months were 68%, 77%, and 84%, respectively. Patients with 3 L CAR-T/4 L lonca had an ORR of 78% (CR rate of 17%). With a median follow-up of 13 months following lonca initiation, the median DOR and PFS were 7.6 and 12.0 months, while median OS was not reached. OS at 12 months was 95%. In this study, we found that lonca monotherapy was an effective treatment option in R/R DLBCL in 3 L and 4 L settings including those who were resistant to or progressed after CAR-T.

摘要

在嵌合抗原受体 T 细胞疗法 (CAR-T) 进展/失败后,loncastuximab tesirine(lonca)的疗效尚不清楚。因此,我们试图在美国研究复发/难治性(R/R)弥漫性大 B 细胞淋巴瘤(DLBCL)患者在接受 CAR-T 治疗后使用 lonca 的真实世界应用和结果。在这项回顾性研究中,我们纳入了接受 lonca 单药治疗的 R/R DLBCL 成年患者(年龄≥18 岁),这些患者在接受二线(2L)或三线(3L)CAR-T 治疗后进展,分别为三线(3L)或四线(4L)治疗。CAR-T 后 lonca 的结果包括缓解率(总缓解率 [ORR] 和完全缓解率 [CR])、缓解持续时间(DOR)、无进展生存期(PFS)和总生存期(OS)。共纳入 118 例患者进行分析,其中 95 例患者在接受 2L CAR-T 后接受 lonca 治疗(中位年龄:66 岁;61%为男性),23 例患者在接受 3L CAR-T 后接受 lonca 治疗(中位年龄:57 岁;43%为男性)。接受 2L CAR-T/3L lonca 的患者 ORR 为 73%(CR 率为 34%)。在 lonca 起始后中位随访 8.5 个月时,中位 DOR、PFS 和 OS 均未达到。12 个月时的 DOR、PFS 和 OS 分别为 68%、77%和 84%。接受 3L CAR-T/4L lonca 的患者 ORR 为 78%(CR 率为 17%)。在 lonca 起始后中位随访 13 个月时,中位 DOR 和 PFS 分别为 7.6 个月和 12.0 个月,中位 OS 未达到。12 个月时的 OS 为 95%。在这项研究中,我们发现 lonca 单药治疗在 3L 和 4L 环境中是 R/R DLBCL 的一种有效治疗选择,包括对 CAR-T 耐药或进展的患者。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d82/11604956/416012fa8133/41408_2024_1195_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d82/11604956/416012fa8133/41408_2024_1195_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d82/11604956/416012fa8133/41408_2024_1195_Fig1_HTML.jpg

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