[分子靶向治疗外周t细胞淋巴瘤]。

Kazuyuki Shimada
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引用次数: 0

摘要

外周t细胞淋巴瘤(PTCL)是一种高度异质性的疾病,占恶性淋巴瘤的10%至15%。它包括广泛的疾病类型,包括淋巴结、结外和白血病形式。最近关于PTCL的分子遗传学发现大大加深了我们对这种疾病的认识,导致以前不同的亚型在一个统一的实体下重新分类(例如,t滤泡辅助淋巴瘤)。在治疗方面,CHOP或CHOP样疗法已被广泛采用为一线方案。然而,即使在alk阳性间变性大细胞淋巴瘤(通常预后良好)中,PTCL的预后仍然令人不满意。复发和难治性疾病的极差预后突出了对突破性治疗的迫切需要。近年来,新的治疗方法,包括抗体-药物偶联物、表观遗传修饰剂和免疫细胞疗法,已经改善了一些PTCL患者的临床结果。然而,新方法的最佳使用仍不清楚,基于分子遗传学发现的分层对于实现更有效和更精确的靶向治疗至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Molecular targeted therapy for peripheral T-cell lymphoma].

Peripheral T-cell lymphoma (PTCL) is a highly heterogenous disease that accounts for 10 to 15% of malignant lymphomas. It encompasses a wide range of disease types, including nodal, extranodal, and leukemic forms. Recent molecular genetic findings about PTCL have significantly deepened our understanding of the disease, leading to the reclassification of previously distinct subtypes under a unified entity (e.g., T-follicular helper lymphoma). In terms of treatment, CHOP or CHOP-like therapy have been widely adopted as a first-line regimen. However, even in ALK-positive anaplastic large cell lymphoma, which generally has favorable outcomes, the prognosis of PTCL remains unsatisfactory. The extremely poor outcomes of relapsed and refractory disease have highlighted an urgent need for breakthrough therapies. In recent years, novel therapeutic approaches, including antibody-drug conjugates, epigenetic modifiers, and immune cell therapies, have improved clinical outcomes for some patients with PTCL. However, the optimal use of novel approaches remains unclear, and stratification based on molecular genetic findings is crucial to achieve more effective and precisely targeted treatment.

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