Jean-Louis Gaston, Cherng Hua-Jay J
Division of Hematology/Oncology, Columbia University Irving Medical Center, New York, NY 10032, USA.
Cancers (Basel). 2025 Mar 29;17(7):1153. doi: 10.3390/cancers17071153.
The introduction of bispecific antibodies (BsAbs) has led to significant improvements in survival for patients with relapsed and refractory B-cell lymphomas. Despite these advances, there remains a significant number of patients who experience disease progression after these novel therapies. Predicting which patients may respond to certain treatments and the durability of their responses remains challenging. Measurable residual disease (MRD) has become easier to detect and quantify through the use of genomic next-generation sequencing tools and has been studied as a possible biomarker to predict long-term outcomes and risk-stratify patients after BsAb therapy in several lymphoma subtypes. Here, we review recent data demonstrating that MRD negativity is associated with radiographic response and improved progression-free survival. Because of heterogeneity in assay choice, assessment timing, and technical parameters, further work is needed before MRD testing is ready to be incorporated into clinical practice in the context of BsAb treatment for B-cell lymphomas.
双特异性抗体(BsAbs)的引入显著提高了复发和难治性B细胞淋巴瘤患者的生存率。尽管取得了这些进展,但仍有相当数量的患者在接受这些新型治疗后出现疾病进展。预测哪些患者可能对特定治疗有反应以及反应的持久性仍然具有挑战性。通过使用基因组下一代测序工具,可测量残留疾病(MRD)变得更容易检测和量化,并且在几种淋巴瘤亚型中,MRD已被作为一种可能的生物标志物进行研究,以预测BsAb治疗后患者的长期预后并进行风险分层。在此,我们回顾了近期数据,这些数据表明MRD阴性与影像学反应及无进展生存期改善相关。由于检测方法选择、评估时间和技术参数存在异质性,在MRD检测准备好纳入B细胞淋巴瘤BsAb治疗的临床实践之前,还需要进一步的研究。