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大 B 细胞淋巴瘤的治疗:社区与学术机构中的当前策略和未满足需求

英文原题:Treating large B-cell lymphoma: Current strategies and unmet needs across community and academic settings.

查看英文原题

Treating large B-cell lymphoma: Current strategies and unmet needs across community and academic settings.

PubMed 2026/06/26(内容时间) Blood Rev Q1 · IF 7.2(JCR 2025)

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中文摘要

大B细胞淋巴瘤(LBCL)的治疗进展迅速,但新疗法的开发和可及性主要集中于学术医疗中心。多数患者在社区医疗系统接受治疗,而资源、基础设施和新疗法可及性较有限,可能影响患者结局。本叙述性综述总结复发/难治性(R/R)LBCL患者的现行治疗策略和真实世界结局。基于polatuzumab的方案仍是前线治疗中高危疾病的标准治疗,并可带来持久应答;然而,约30%–40%的患者会出现复发/难治性疾病。CAR-T 细胞疗法具有治愈潜力,但其应用受物流、社会经济和地理因素限制。双特异性抗体和抗体药物偶联物等新型疗法可能改善社区医疗环境中的治疗可及性。我们还讨论影响治疗策略的患者层面和诊疗实践因素、未满足的临床需求,以及社区医疗中心与学术中心合作以优化R/R LBCL患者结局的必要性。

展开英文摘要原文

Therapeutic advances in large B-cell lymphoma (LBCL) are rapidly emerging, but their development and availability are largely concentrated in academic centers. Most patients receive care within community health systems where more limited resources, infrastructure, and access to novel treatments may influence outcomes. This narrative review summarizes current treatment strategies and real-world outcomes for patients with relapsed or refractory (R/R) LBCL.

Polatuzumab-based regimens remain standard for high-risk disease in the frontline setting and achieve durable responses; however, approximately 30-40% of patients experience R/R disease. While chimeric antigen receptor T-cell therapy offers curative potential, its use is constrained by logistical, socioeconomic, and geographic barriers. Novel therapies, including bispecific antibodies and antibody-drug conjugates, may improve treatment access in community settings.

We also discuss patient- and practice-level factors affecting treatment strategies, unmet clinical needs, and the need for collaboration between community and academic centers in optimizing outcomes for patients with R/R LBCL.

论文信息

作者
Graff T、Pearson E、Ahmed S、Patel K、Lunning M
单位
Mission Cancer and Blood/UIHSMG, Waukee, IA, USA. Electronic address: tgraff@missioncancer.com.United States
文献类型
综述
期刊
Blood reviews2026 Jul
原文标识
PubMed 42379984 · DOI 10.1016/j.blre.2026.101415