Shanafelt Tait D
Hematology. 2012 Apr;17 Suppl 1:S133-6. doi: 10.1179/102453312X13336169156410.
The last two decades have been time of tremendous progress in treatment for patients with chronic lymphocytic lymphoma (CLL). Chemoimmunotherapy (CIT) combining anti-CD20 monoclonal antibodies with purine nucleoside analogs has been a substantial advance for patients with CLL and results in increased response rates, progression-free survival, and overall survival. Despite these improved outcomes, only ≈ 45% of patients achieve a complete remission with CIT and nearly all patients eventually relapse and their remains a need to improve efficacy. Although new combinations of traditional agents may lead to incremental progress, more substantive improvements are likely to result through therapeutic targeting of novel pathways critical to CLL B-cell survival including targeting: (1) leukemia cell apoptotic resistance; (2) survival signals mediated through the B-cell receptor; and (3) nurturing interactions with the microenvironment. In this mini-review, we summarize Mayo Clinic's recent efforts to improve CIT for patients with CLL.
过去二十年是慢性淋巴细胞白血病(CLL)患者治疗取得巨大进展的时期。将抗CD20单克隆抗体与嘌呤核苷类似物联合使用的化学免疫疗法(CIT),对于CLL患者而言是一项重大进展,可提高缓解率、无进展生存期和总生存期。尽管有这些改善的结果,但只有约45%的患者通过CIT实现完全缓解,几乎所有患者最终都会复发,因此仍需要提高疗效。虽然传统药物的新组合可能会带来渐进式进展,但通过针对对CLL B细胞存活至关重要的新途径进行治疗性靶向,包括靶向:(1)白血病细胞凋亡抗性;(2)通过B细胞受体介导的存活信号;以及(3)与微环境的滋养相互作用,更有可能带来实质性的改善。在本综述中,我们总结了梅奥诊所最近为改善CLL患者CIT所做的努力。