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在输注 tisagenlecleucel 之前采取有效的桥接策略可使复发/难治性大 B 细胞淋巴瘤获得高反应率和长期缓解:来自德国单中心研究的结果。

Effective bridging strategies prior to infusion with tisagenlecleucel results in high response rates and long-term remission in relapsed/refractory large B-cell lymphoma: findings from a German monocentric study.

机构信息

Klinik Für Innere Medizin II, Abteilung für Hämatologie und Internistische Onkologie, Universitätsklinikum Jena, Am Klinikum 1, 07747, Jena, Germany.

Comprehensive Cancer Center Central Germany (CCCG) Jena/Leipzig, Campus Jena, Jena, Germany.

出版信息

J Cancer Res Clin Oncol. 2024 May 1;150(5):224. doi: 10.1007/s00432-024-05765-8.

Abstract

BACKGROUND

Incorporating chimeric antigen receptor (CAR)-T cell therapy into relapsed or refractory large B-cell lymphoma (rr LBCL) treatment algorithms has yielded remarkable response rates and durable remissions, yet a substantial portion of patients experience progression or relapse. Variations in outcomes across treatment centers may be attributed to different bridging strategies and remission statuses preceding CAR-T cell therapy.

PATIENTS

Twenty-nine consecutive adult patients receiving tisagenlecleucel (tisa-cel) for rr LBCL from December 2019 to February 2023 at Jena University Hospital were analyzed.

RESULTS

The median age was 63, with a median of 3 prior treatments. Twenty patients (69%) were refractory to any systemic therapy before CAR-T cell treatment. Following leukapheresis, 25 patients (86%) received bridging therapy with the majority undergoing chemotherapy (52%) or combined modality therapy (32%). Radiotherapy (RT) was part of the bridging strategy in 44%, with moderately hypofractionated involved site RT (30.0 Gy/2.5 Gy) being applied most frequently (64%). Post-CAR-T infusion, the objective response rate at 30 days was 83%, with 55% achieving complete response. Twelve-month progression-free (PFS) and overall survival (OS) were 60% and 74%, respectively, with a median follow up of 11.1 months for PFS and 17.9 months for OS. Factors significantly associated with PFS were chemotherapy sensitivity pre-leukapheresis and response to bridging.

CONCLUSION

The study underscores the importance of minimal tumor burden at CAR-T initiation, emphasizing the need for suitable bridging regimens. The findings advocate for clinical trials and further real-world analyses to optimize CAR-T cell therapy outcomes by identifying the most effective bridging strategies.

摘要

背景

嵌合抗原受体 (CAR)-T 细胞疗法被纳入复发或难治性大 B 细胞淋巴瘤 (rr LBCL) 的治疗方案中,取得了显著的缓解率和持久的缓解,但仍有相当一部分患者出现进展或复发。治疗中心之间的结果差异可能归因于不同的桥接策略和 CAR-T 细胞治疗前的缓解状态。

患者

2019 年 12 月至 2023 年 2 月,在耶拿大学医院接受 tisagenlecleucel (tisa-cel) 治疗的 29 例连续成年 rr LBCL 患者进行了分析。

结果

中位年龄为 63 岁,中位治疗次数为 3 次。20 例患者(69%)在接受 CAR-T 细胞治疗前对任何系统性治疗均有耐药性。在外周血干细胞采集后,25 例患者(86%)接受了桥接治疗,大多数接受了化疗(52%)或联合治疗(32%)。44%的桥接策略中包含放疗(RT),最常采用中度分割局部 RT(30.0Gy/2.5Gy)(64%)。CAR-T 输注后 30 天的客观缓解率为 83%,55%达到完全缓解。12 个月无进展生存率(PFS)和总生存率(OS)分别为 60%和 74%,中位随访时间分别为 PFS 为 11.1 个月和 OS 为 17.9 个月。与 PFS 显著相关的因素是外周血干细胞采集前的化疗敏感性和桥接治疗的反应。

结论

该研究强调了 CAR-T 起始时肿瘤负荷最小的重要性,强调了需要合适的桥接方案。这些发现支持进行临床试验和进一步的真实世界分析,通过确定最有效的桥接策略来优化 CAR-T 细胞治疗的结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/554d/11793443/6d94a770fa36/432_2024_5765_Fig1_HTML.jpg

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