Role of bridging RT in relapsed/refractory diffuse large B-cell lymphoma undergoing CAR-T therapy: a multicenter study

桥接(联网) 医学 内科学 淋巴瘤 养生 耐火材料(行星科学) 化疗 放射治疗 胃肠病学 外科 肿瘤科 计算机网络 物理 天体生物学 计算机科学
作者
Daniele Mannina,Stéfania Bramanti,Annalisa Chiappella,Beatrice Casadei,Chiara De Philippis,Laura Giordano,Pierina Navarria,Pietro Mancosu,Daniela Taurino,Marta Scorsetti,Carmelo Carlo‐Stella,Pier Luigi Zinzani,Armando Santoro,Paolo Corradini
出处
期刊:Research Square - Research Square
标识
DOI:10.21203/rs.3.rs-3573162/v1
摘要

Abstract The optimization of bridging regimen before chimeric antigen receptor (CAR)-T cell therapy in diffuse large B-cell lymphoma (DLBCL) may impact CAR-T efficacy and outcome. This retrospective study evaluates CAR-T outcome after bridging with radiotherapy (RT) and other bridging strategies. Among 148 patients with relapsed/refractory DLBCL who underwent leukapheresis for CAR-T manufacturing, 31 received RT-bridging, 84 chemotherapy (CT), 33 no-bridging or steroid-only. CAR-T cell were infused in 96.8% of RT-group. 89.2% of CT-group and 78.8% of no-bridge group (p = 0.079). Response to bridging was generally poor, but patients receiving RT had a significant reduction in LDH levels between pre- and post-bridging (p = 0.05). The one-year PFS was 51.2% in the RT group, 28.2% in the CT group, and 47.6% in the no-bridge group (p = 0.044); 1-year OS was 86.7% in the RT group, 52.7% in the CT group and 69% in the no-bridge group (p = 0.025). We observed a higher incidence of ICANS in patients who received CT than in others (20.0% CT group, 3.3% RT group, 7.7% no-bridge group; p = 0.05). In conclusion, RT-bridging is associated with lower drop-out rate and CAR-T toxicity, and it might be preferred to other bridging strategies for patients with localized disease or for those with one prevalent symptomatic site.
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