Hematology Department, Hospices Civils de Lyon and Université Lyon 1, Lyon, France.
Int J Hematol. 2010 Jul;92(1):12-24. doi: 10.1007/s12185-010-0609-6. Epub 2010 Jun 18.
The outcome of patients with diffuse large B cell lymphoma (DLBCL) has completely changed with the introduction of rituximab in combination with chemotherapy. This was the first targeted therapy, and it led the way to new antibodies targeting cell surface receptors and to small molecules targeting one or several key proteins of the cellular machinery. Those new therapeutic small molecules are targeting the different pathways of apoptosis, proteasome inhibitors, immunomodulators, histone deacetylase inhibitors, mammalian target of rapamycin inhibitors, heat shock protein inhibitors, PKC inhibitors, antiangiogenic agents, Syk inhibitors, and farnesyl transferase inhibitors. The new monoclonal antibodies target CD20, CD22, CD19, CD40, CD74, and HLA Drbeta. Although the majority of them have been studied in mixed subtypes of B cell lymphoma, the aim of this review was to present major results in clinical studies for these new agents in DLBCL patients, and for those that have just entered clinical evaluation, the results of pre-clinical studies in DLBCL lines.
随着利妥昔单抗联合化疗在弥漫性大 B 细胞淋巴瘤(DLBCL)中的应用,患者的预后发生了根本改变。这是首个靶向治疗药物,为针对细胞表面受体的新型抗体以及针对细胞机制中一个或几个关键蛋白的小分子药物铺平了道路。这些新的治疗性小分子药物靶向不同的凋亡途径、蛋白酶体抑制剂、免疫调节剂、组蛋白去乙酰化酶抑制剂、哺乳动物雷帕霉素抑制剂、热休克蛋白抑制剂、PKC 抑制剂、抗血管生成剂、Syk 抑制剂和法呢基转移酶抑制剂。新型单克隆抗体靶向 CD20、CD22、CD19、CD40、CD74 和 HLA Drbeta。尽管其中大多数药物已在混合亚型 B 细胞淋巴瘤中进行了研究,但本篇综述的目的是介绍这些新药物在 DLBCL 患者中的临床试验中的主要结果,以及那些刚刚进入临床评估阶段的药物在 DLBCL 细胞系中的临床前研究结果。