Krug Adrien, Tari Gamze, Saidane Aymen, Gaulard Philippe, Ricci Jean-Ehrland, Lemonnier François, Verhoeyen Els
Université Côte d'Azur, INSERM, C3M, 06204 Nice, France.
Univ Paris Est Créteil, INSERM, IMRB, 94010 Créteil, France.
Cancers (Basel). 2022 May 12;14(10):2392. doi: 10.3390/cancers14102392.
The classification of peripheral T-cell lymphomas (PTCL) is constantly changing and contains multiple subtypes. Here, we focus on Tfh-like PTCL, to which angioimmunoblastic T-cell lymphoma (AITL) belongs, according to the last WHO classification. The first-line treatment of these malignancies still relies on chemotherapy but gives very unsatisfying results for these patients. Enormous progress in the last decade in terms of understanding the implicated genetic mutations leading to signaling and epigenetic pathway deregulation in Tfh PTCL allowed the research community to propose new therapeutic approaches. These findings point towards new biomarkers and new therapies, including hypomethylating agents, such as azacytidine, and inhibitors of the TCR-hyperactivating molecules in Tfh PTCL. Additionally, metabolic interference, inhibitors of the NF-κB and PI3K-mTOR pathways and possibly novel immunotherapies, such as antibodies and chimeric antigen receptors (CAR) directed against Tfh malignant T-cell surface markers, are discussed in this review among other new treatment options.
外周T细胞淋巴瘤(PTCL)的分类一直在变化,包含多种亚型。在此,我们聚焦于滤泡辅助性T细胞样PTCL,根据世界卫生组织的最新分类,血管免疫母细胞性T细胞淋巴瘤(AITL)属于此类。这些恶性肿瘤的一线治疗仍依赖化疗,但对这些患者而言效果非常不理想。在过去十年中,在理解导致Tfh PTCL中信号传导和表观遗传途径失调的相关基因突变方面取得了巨大进展,这使得研究界能够提出新的治疗方法。这些发现指向了新的生物标志物和新的疗法,包括低甲基化剂,如阿扎胞苷,以及Tfh PTCL中TCR过度激活分子的抑制剂。此外,本综述还讨论了代谢干扰、NF-κB和PI3K-mTOR途径的抑制剂以及可能的新型免疫疗法,如针对Tfh恶性T细胞表面标志物的抗体和嵌合抗原受体(CAR)等其他新的治疗选择。