【滤泡性淋巴瘤的分子发病机制及治疗】。

Momoko Nishikori
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引用次数: 0

摘要

滤泡性淋巴瘤(FL)具有广泛的临床表现,从很少或不需要治疗的病例到任何治疗都难治的病例。近年来,DNA和RNA谱分析以及肿瘤微环境分析的进展,逐渐增加了对FL潜在分子发病机制的理解。免疫化疗后疾病的早期进展包括组织学转变为更具侵袭性的表型,这与较差的生存结果相关。除了传统的免疫化疗之外,包括小分子化合物、双特异性抗体和CAR-T细胞治疗在内的最新进展扩大了FL患者的治疗选择并改善了预后。研究表明,与治疗效果和预后相关的因素可能在不同的治疗药物中不一致。更深入地了解FL的分子生物学应该为优化、个性化的治疗序列铺平道路。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Molecular pathogenesis and treatment of follicular lymphoma].

Follicular lymphoma (FL) has a wide spectrum of clinical manifestations, ranging from cases that require little or no treatment to cases that are refractory to any treatment. In recent years, advances in DNA and RNA profiling, as well as analysis of the tumor microenvironment, have progressively increased understanding of the underlying molecular pathogenesis of FL. Early progression of disease following immunochemotherapy includes histologic transformation to a more aggressive phenotype, which is associated with poor survival outcomes. Recent advances beyond conventional immunochemotherapy, including small molecular compounds, bispecific antibodies, and CAR-T cell therapy, have expanded therapeutic options and improved prognosis for FL patients. Research suggests that factors associated with treatment efficacy and prognosis may not be consistent across therapeutic agents. A deeper understanding of the molecular biology of FL should pave the way for optimized, individualized treatment sequences.

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