Brighton and Sussex Medical School, University of Sussex, Brighton, BN1 9PS, UK.
Royal Sussex County Hospital, Eastern Road, Brighton, BN2 5BE, UK.
Curr Oncol Rep. 2020 Mar 14;22(4):36. doi: 10.1007/s11912-020-0893-0.
Chronic lymphocytic leukaemia is now recognised as a heterogenous disease with a variety of clinical outcomes. Here we summarise the way it is currently stratified according to genetic risk and patient characteristics and the treatment approaches used for these different subgroups.
Certain patients appear to sustain MRD negativity after combination chemoimmunotherapy, leading to the suggestion that their CLL may be cured. However, 17p-deleted, p53-mutated or IGHV-UM subgroups are generally resistant to FCR, and much better responses are seen with ibrutinib and venetoclax, frequently inducing MRD negativity that hopefully will be translated into durable remissions. Small molecule inhibitors have already revolutionised CLL treatment. Going forward, we anticipate their use in the majority of patients, early after diagnosis and with curative intent.
慢性淋巴细胞白血病(CLL)现已被认为是一种异质性疾病,具有多种临床转归。目前,我们根据遗传风险和患者特征对其进行了分类,并对不同亚组的治疗方法进行了总结。
某些患者在联合化疗免疫治疗后似乎持续达到微小残留病灶(MRD)阴性,这提示其 CLL 可能被治愈。然而,17p 缺失、p53 突变或 IGHV-未突变亚组通常对 FCR 耐药,而伊布替尼和维奈托克的反应更好,常诱导 MRD 阴性,有望转化为持久缓解。小分子抑制剂已彻底改变了 CLL 的治疗方法。展望未来,我们预计它们将在大多数患者中得到应用,在诊断后早期即开始,并以治愈为目的。