Department of Lymphoma and Myeloma, the University of Texas MD Anderson Cancer Center, 1515 Holcombe Boulevard Unit 0429, Houston, TX 77030-4009, USA.
Sci Signal. 2019 Feb 5;12(567):eaat4105. doi: 10.1126/scisignal.aat4105.
Mantle cell lymphoma (MCL) is an aggressive B cell lymphoma that is largely chemoresistant. Ibrutinib, a drug that inhibits Bruton's tyrosine kinase (BTK), has improved the overall survival of patients with MCL; however, resistance to ibrutinib has emerged as a decisive, negative factor in the prognosis of MCL. Adopting a more patient-centric therapeutic approach that incorporates applied genomics and interrogation of B cell signaling pathways may offer an alternative route to reach durable remission in patients with MCL. Although targeting genetic variants in MCL is not yet feasible in the clinical setting, the identification and targeting of increasingly active B cell signaling pathways may be a viable therapeutic strategy that may improve patient outcomes. Genome-editing tools and sequencing platforms could play dominant roles in patient-centric approaches of treatment in the future, potentially improving clinical outcomes for patients with MCL.
套细胞淋巴瘤(MCL)是一种侵袭性 B 细胞淋巴瘤,对化疗有很大的耐药性。伊布替尼是一种抑制布鲁顿酪氨酸激酶(BTK)的药物,它改善了 MCL 患者的总生存率;然而,对伊布替尼的耐药性已成为影响 MCL 预后的决定性负面因素。采用更加以患者为中心的治疗方法,结合应用基因组学和 B 细胞信号通路的检测,可能为 MCL 患者获得持久缓解提供另一种途径。尽管在临床环境中针对 MCL 的遗传变异进行靶向治疗尚不可行,但识别和靶向越来越活跃的 B 细胞信号通路可能是一种可行的治疗策略,可能改善患者的预后。基因组编辑工具和测序平台在未来的以患者为中心的治疗方法中可能发挥主导作用,有可能改善 MCL 患者的临床结局。