Piotr Smolewski, Magdalena Witkowska, Anna Korycka-Wołowiec
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引用次数: 0
摘要
慢性淋巴细胞白血病(CLL)的特点是成熟 B 淋巴细胞的克隆增殖和积累。CLL 细胞具有抗凋亡特性,这表明抑制凋亡在疾病发展中起着重要作用。不过,也有一些增殖的 CLL 细胞,它们也可能在疾病的发展过程中发挥作用。CLL有几种较新的生物学预后因素。目前,具有不同预后价值的细胞遗传学异常似乎是最具生物学相关性的因素。在过去的几十年中,CLL 的治疗方法发生了重大变化。不同的治疗策略相继问世,如单独使用氯霉素和嘌呤核苷类似物(PNA)或与环磷酰胺联合使用。最近,抗CD20单克隆抗体利妥昔单抗联合氟达拉滨和环磷酰胺的免疫化学疗法成为符合条件的CLL患者一线治疗的金标准。目前,新的治疗策略,包括新的单克隆抗体、苯达莫司汀、来那度胺或多种细胞信号通路抑制剂,正在耐药/复发的CLL患者中进行临床研究。此外,还必须考虑异基因干细胞移植,尤其是年轻的高危患者,如对PNA耐药或有17p缺失的患者。在本文中,我们将介绍CLL生物学和治疗方面最重要的最新进展。
New insights into biology, prognostic factors, and current therapeutic strategies in chronic lymphocytic leukemia.
Chronic lymphocytic leukemia (CLL) is characterized by the clonal proliferation and accumulation of mature B lymphocytes. CLL cells show an antiapoptotic profile, suggesting the important role of apoptosis inhibition in the disease development. However, there is some population of proliferating CLL cells, which may also play a role in progression of the disease. There are several newer, biological prognostic factors in CLL. Currently, cytogenetic abnormalities with different prognostic values seem to be the most biologically relevant. During the last decades, the treatment of CLL has been significantly changed. Different strategies such as monotherapy with chlorambucil and purine nucleoside analogues (PNA) used alone or in combination with cyclophosphamide have been introduced. Most recently, immunochemotherapy with anti-CD20 monoclonal antibody, rituximab, combined with fludarabine and cyclophosphamide, became a gold standard of first-line treatment in eligible CLL patients. Currently, new treatment strategies including new monoclonal antibodies, bendamustine, lenalidomide, or inhibitors of several cell signaling pathways are under clinical studies in resistant/relapsed CLL patients. Moreover, allogeneic stem cell transplantation has to be considered, especially in younger high risk patients, for example, those who are resistant to PNA or those with 17p deletion. In this paper, we present the most important recent advances in CLL biology and treatment.