Mina Alain, Pro Barbara
Robert H. Lurie Comprehensive Cancer Center, Northwestern University, Chicago, IL, USA; Division of Hematology-Oncology, Department of Medicine, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.
Blood Rev. 2022 Mar;52:100889. doi: 10.1016/j.blre.2021.100889. Epub 2021 Sep 9.
Peripheral T-cell Lymphomas (PTCL) are a heterogenous group of aggressive non-Hodgkin lymphomas that are far less sensitive to chemotherapy than their B-cell counterparts. Despite their poor prognosis, they are treated similarly to most aggressive B-cell lymphomas, heavily relying on CHOP or CHOP-like combination chemotherapy irrespective of their different subtypes or biology. The last decade has seen the emergence of many targeted therapies that include histone deacetylase inhibitors, hypomethylating agents, monoclonal antibodies and PIK3 inhibitors, among others. However, prognosis remains poor especially in the relapsed/refractory setting. Using an extensive pubmed search, the authors will be summarizing the different trials that led to these approved targeted agents as well as novel combination strategies. The fundamental recognition that different subtypes of PTCL have specific biological features that drive not only proliferation, but also responses to different treatment approaches, should be informing the design of future clinical trials.
外周T细胞淋巴瘤(PTCL)是一组异质性侵袭性非霍奇金淋巴瘤,与B细胞淋巴瘤相比,它们对化疗的敏感性要低得多。尽管其预后较差,但它们的治疗方式与大多数侵袭性B细胞淋巴瘤相似,严重依赖CHOP或类似CHOP的联合化疗,而不考虑其不同的亚型或生物学特性。在过去十年中,出现了许多靶向治疗方法,包括组蛋白去乙酰化酶抑制剂、低甲基化剂、单克隆抗体和PIK3抑制剂等。然而,预后仍然很差,尤其是在复发/难治性情况下。通过广泛的PubMed搜索,作者将总结导致这些获批靶向药物的不同试验以及新的联合策略。认识到PTCL的不同亚型具有特定的生物学特征,这些特征不仅驱动细胞增殖,还影响对不同治疗方法的反应,这一基本认识应为未来临床试验的设计提供依据。