Wallington David G, Imber Brandon S, Scordo Michael, Robinson Timothy J
Department of Therapeutic Radiology, Yale Cancer Center, New Haven, CT.
Department of Radiation Oncology, Memorial Sloan Kettering Cancer Center, New York, NY.
Semin Radiat Oncol. 2025 Jan;35(1):99-109. doi: 10.1016/j.semradonc.2024.10.005.
Chimeric antigen receptor (CAR) T-cell receptor therapy has transformed outcomes for patients with relapsed and refractory diffuse large B-cell lymphoma (R/R DLBCL). It is currently approved in the third line for all patients and in the second line for early relapsed or primary refractory disease. Although CAR T cell therapy offers the potential for improved outcomes, its use may also include logistical delays related to referral, medical, social, and financial clearance as well as manufacturing time; more than half of patients experience disease recurrence or progression while awaiting CAR T infusion. Bridging radiotherapy, defined as radiation delivered between the decision to pursue CAR T and infusion of CAR T cells, has become an attractive option for patients who would benefit from local disease control or palliation of symptoms. Additionally, patterns of failure analyses have revealed a dominant role of local disease progression, which has fueled investigations on bridging and early salvage radiation to improve long-term outcomes in patients, particularly those with localized or high-risk disease. Several potential mechanisms by which radiation therapy may improve CAR T efficacy have been proposed that include cytoreduction, tumor debulking, neutralization of immunosuppressive hypoxic and acidic tumor microenvironments, and immunologic and pro-apoptotic synergy between radiation and CAR T. Prospective clinical trials and translational work are ongoing and are needed to inform our conceptual understanding of potential mechanisms by which radiation therapy may improve CAR T efficacy and toxicity, identify which patients may be most likely to benefit, and confirm proposed clinical benefits.
嵌合抗原受体(CAR)T细胞受体疗法已经改变了复发难治性弥漫性大B细胞淋巴瘤(R/R DLBCL)患者的治疗结局。目前,该疗法已被批准用于所有患者的三线治疗以及早期复发或原发性难治性疾病的二线治疗。尽管CAR T细胞疗法有可能改善治疗结局,但其应用可能还会涉及与转诊、医疗、社会和财务审批以及生产时间相关的后勤延迟;超过半数的患者在等待CAR T输注期间会出现疾病复发或进展。桥接放疗,即指在决定采用CAR T疗法至输注CAR T细胞之间进行的放疗,对于那些将从局部疾病控制或症状缓解中获益的患者而言,已成为一种颇具吸引力的选择。此外,失败模式分析显示局部疾病进展起主要作用,这推动了对桥接放疗和早期挽救性放疗的研究,以改善患者的长期结局,尤其是那些患有局限性或高危疾病的患者。已经提出了放疗可能提高CAR T疗效的几种潜在机制,包括细胞减灭、肿瘤减积、中和免疫抑制性缺氧和酸性肿瘤微环境,以及放疗与CAR T之间的免疫和促凋亡协同作用。前瞻性临床试验和转化研究正在进行中,并且需要这些研究来增进我们对放疗可能提高CAR T疗效和毒性的潜在机制的概念性理解,确定哪些患者最有可能从中获益,并确认所提出的临床益处。