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Novel therapy for Hodgkin lymphoma

机译:霍奇金淋巴瘤的新疗法

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摘要

The treatment of Hodgkin lymphoma (HL) relies on multimodality treatment with standard chemotherapy, radiation therapy, and autologous or allogeneic stem cell transplantation in cases of relapsed disease. Genomic advances in HL provided insights into deregulation of key nodal signaling pathways, including the PI3K, NF-κB, and JAK/STAT pathways, which are amenable to small-molecule targeting. Understanding how HL cells interact and depend on their microenvironment for survival signals and immune protection may uncover other such pathways. Small-molecule targeting has the potential to dramatically improve treatment outcomes, especially in patients with highly refractory disease and those with poor tolerance to existing chemotherapies. As novel therapies continue to be developed for HL, the challenge will be to address the needs of high-risk groups, reduce long-term therapy-related morbidity, position current established treatments with novel therapies, and concurrently develop biomarkers to aid in patient selection. Brentuximab vedotin, which was approved in 2011, is already shifting the treatment paradigm of HL. Undoubtedly, other novel therapeutics in the pipeline will affect positively the landscape of treatment in HL.
机译:霍奇金淋巴瘤(HL)的治疗依赖于标准疗法,放射疗法和自体或异体干细胞移植的多模式治疗,以预防复发性疾病。 HL基因组学的进步提供了对关键节点信号转导通路放松调控的见识,这些通路包括适合小分子靶向的PI3K,NF-κB和JAK / STAT通路。了解HL细胞如何相互作用并依赖其微环境获取生存信号和免疫保护,可能会发现其他此类途径。小分子靶向治疗有可能显着改善治疗效果,特别是在高难治性疾病患者和对现有化学疗法耐受性差的患者中。随着针对HL的新疗法的不断开发,挑战将是解决高风险人群的需求,减少与长期疗法相关的发病率,使用新疗法定位当前已建立的疗法以及同时开发生物标记物以帮助患者选择。于2011年获准使用的Brentuximab vedotin已经改变了HL的治疗方式。毫无疑问,其他正在开发中的新疗法将对HL的治疗前景产生积极影响。

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