Scholarlink

<p>Angioimmunoblastic T-cell lymphoma (AITL) is a subtype of peripheral T-cell lymphoma originating from follicular helper T cells and characterized by profound clinical, pathological, and molecular heterogeneity. Despite advances in classification and diagnosis, therapeutic outcomes remain suboptimal, particularly in relapsed or refractory settings. In recent years, the evolution of risk stratification models and a deeper understanding of AITL’s molecular pathogenesis, including its unique pattern of clonal evolution, have paved the way for precision medicine. Notably, targeted treatment approaches, such as immunomodulatory agents, epigenetic therapies, kinase inhibitors, and immune checkpoint blockade, are demonstrating promising clinical efficacy, especially in patients harboring specific molecular aberrations. This review comprehensively summarizes the multilayered heterogeneity of AITL, emphasizes the role of immune and molecular profiling in informing therapeutic decisions, and outlines future directions for personalized, multi-agent treatment strategies aimed at overcoming resistance and improving survival.</p>

错误：搜索内容不能为空，请输入英文关键词
错误：关键词超出字数限制，请精简
高级检索

Unraveling the many faces of angioimmunoblastic T-cell lymphoma: clinical, pathological, and molecular heterogeneity

  • 期刊论文

  • 出版模式：

    开放获取

  • 发表日期：

    2026年1月15日

查看全文
  • Jia-Ping Chen,
  • Peng Ke,
  • Xiao Qiu,
  • Qiu-Yuan Xian,
  • Jing-Song Wu,
  • Chun Feng,
  • Hui-Jun Li,
  • Yang Wang,
  • Ji-Hao Zhou

摘要

Angioimmunoblastic T-cell lymphoma (AITL) is a subtype of peripheral T-cell lymphoma originating from follicular helper T cells and characterized by profound clinical, pathological, and molecular heterogeneity. Despite advances in classification and diagnosis, therapeutic outcomes remain suboptimal, particularly in relapsed or refractory settings. In recent years, the evolution of risk stratification models and a deeper understanding of AITL’s molecular pathogenesis, including its unique pattern of clonal evolution, have paved the way for precision medicine. Notably, targeted treatment approaches, such as immunomodulatory agents, epigenetic therapies, kinase inhibitors, and immune checkpoint blockade, are demonstrating promising clinical efficacy, especially in patients harboring specific molecular aberrations. This review comprehensively summarizes the multilayered heterogeneity of AITL, emphasizes the role of immune and molecular profiling in informing therapeutic decisions, and outlines future directions for personalized, multi-agent treatment strategies aimed at overcoming resistance and improving survival.