Phase II Trial of Hypofractionated Radiotherapy and Immunochemotherapy in Primary Refractory Diffuse Large B-Cell Lymphoma: Preliminary Results and Insights from Digital Spatial Profiling

IF 10.7 Q1 MEDICINE, RESEARCH & EXPERIMENTAL
MedComm Pub Date : 2025-05-25 DOI:10.1002/mco2.70225
Yong Yang, Jing Yu, Xiao-Mei Hu, Si-Lin Chen, Rui-Zhi Zhao, Cheng Huang, Jiang-Rui Guo, Tian-Lan Tang, Cheng Chen, Yu-Ping Lin, Ying Wang, Tian-Xiu Liu, Hao Zheng, Si-Qin Liao, Jin-Hua Chen, Hai-Ying Fu, Ting-Bo Liu
{"title":"Phase II Trial of Hypofractionated Radiotherapy and Immunochemotherapy in Primary Refractory Diffuse Large B-Cell Lymphoma: Preliminary Results and Insights from Digital Spatial Profiling","authors":"Yong Yang,&nbsp;Jing Yu,&nbsp;Xiao-Mei Hu,&nbsp;Si-Lin Chen,&nbsp;Rui-Zhi Zhao,&nbsp;Cheng Huang,&nbsp;Jiang-Rui Guo,&nbsp;Tian-Lan Tang,&nbsp;Cheng Chen,&nbsp;Yu-Ping Lin,&nbsp;Ying Wang,&nbsp;Tian-Xiu Liu,&nbsp;Hao Zheng,&nbsp;Si-Qin Liao,&nbsp;Jin-Hua Chen,&nbsp;Hai-Ying Fu,&nbsp;Ting-Bo Liu","doi":"10.1002/mco2.70225","DOIUrl":null,"url":null,"abstract":"<p>This open-label, single-arm phase II study assessed the safety and efficacy of sequential hypofractionated radiotherapy (RT) followed by zimberelimab and R-GemOx (rituximab, gemcitabine, oxaliplatin) in patients with primary refractory diffuse large B-cell lymphoma (DLBCL). Fourteen patients were enrolled between June 2022 and December 2023, with 13 included in the analysis. RT doses of 36 and 24 Gy were delivered to the gross and target volumes in 12 fractions, followed by zimberelimab and R-GemOx. The overall response rate within the irradiated field was 92.3%, and a complete response (CR) was achieved by 61.5% of patients; however, 38.5% experienced disease progression. Treatment-related toxicities were manageable, primarily comprising mild leukocytopenia. Digital spatial profiling revealed 53 differentially expressed genes in CD20-rich lymphoma regions and 93 in CD3-rich T cell regions in non-CR patients. Reactome analysis identified key immune system pathways. T cell infiltration correlated with treatment efficacy, and multiplex immunohistochemistry validated immune pathways as potential therapeutic targets. This study demonstrated the promising role of RT combined with immunochemotherapy in refractory DLBCL and suggests immune pathways as critical targets to improve treatment outcomes.</p>","PeriodicalId":94133,"journal":{"name":"MedComm","volume":"6 6","pages":""},"PeriodicalIF":10.7000,"publicationDate":"2025-05-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/mco2.70225","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"MedComm","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/mco2.70225","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MEDICINE, RESEARCH & EXPERIMENTAL","Score":null,"Total":0}
引用次数: 0

Abstract

This open-label, single-arm phase II study assessed the safety and efficacy of sequential hypofractionated radiotherapy (RT) followed by zimberelimab and R-GemOx (rituximab, gemcitabine, oxaliplatin) in patients with primary refractory diffuse large B-cell lymphoma (DLBCL). Fourteen patients were enrolled between June 2022 and December 2023, with 13 included in the analysis. RT doses of 36 and 24 Gy were delivered to the gross and target volumes in 12 fractions, followed by zimberelimab and R-GemOx. The overall response rate within the irradiated field was 92.3%, and a complete response (CR) was achieved by 61.5% of patients; however, 38.5% experienced disease progression. Treatment-related toxicities were manageable, primarily comprising mild leukocytopenia. Digital spatial profiling revealed 53 differentially expressed genes in CD20-rich lymphoma regions and 93 in CD3-rich T cell regions in non-CR patients. Reactome analysis identified key immune system pathways. T cell infiltration correlated with treatment efficacy, and multiplex immunohistochemistry validated immune pathways as potential therapeutic targets. This study demonstrated the promising role of RT combined with immunochemotherapy in refractory DLBCL and suggests immune pathways as critical targets to improve treatment outcomes.

低分割放疗和免疫化疗治疗原发性难治性弥漫性大b细胞淋巴瘤的II期试验:初步结果和数字空间分析的见解
这项开放标签、单组II期研究评估了顺序低分割放疗(RT)后使用zimberelimab和R-GemOx(利妥昔单抗、吉西他滨、奥沙利铂)治疗原发性难治性弥漫性大b细胞淋巴瘤(DLBCL)患者的安全性和有效性。在2022年6月至2023年12月期间,14名患者入组,其中13名纳入分析。36和24 Gy的RT剂量分12份递送至总体积和靶体积,随后递送zimberelimab和R-GemOx。辐照场内总有效率为92.3%,完全缓解(CR)率为61.5%;然而,38.5%的患者出现了疾病进展。治疗相关的毒性是可控的,主要包括轻度白细胞减少。数字空间分析显示,非cr患者在富含cd20的淋巴瘤区有53个差异表达基因,在富含cd3的T细胞区有93个差异表达基因。反应组分析确定了关键的免疫系统途径。T细胞浸润与治疗效果相关,多重免疫组织化学证实免疫途径是潜在的治疗靶点。这项研究表明,RT联合免疫化疗在难治性DLBCL中有很好的作用,并表明免疫途径是改善治疗结果的关键靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
CiteScore
6.70
自引率
0.00%
发文量
0
审稿时长
10 weeks
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信