Department of Pediatrics and Adolescent Medicine, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.
Centre for Regenerative Medicine, University of Edinburgh, Edinburgh, UK.
Leukemia. 2022 Dec;36(12):2751-2768. doi: 10.1038/s41375-022-01714-x. Epub 2022 Oct 20.
Delivery of effective anti-leukemic agents to the central nervous system (CNS) is considered essential for cure of childhood acute lymphoblastic leukemia. Current CNS-directed therapy comprises systemic therapy with good CNS-penetration accompanied by repeated intrathecal treatments up to 26 times over 2-3 years. This approach prevents most CNS relapses, but is associated with significant short and long term neurotoxicity. Despite this burdensome therapy, there have been no new drugs licensed for CNS-leukemia since the 1960s, when very limited anti-leukemic agents were available and there was no mechanistic understanding of leukemia survival in the CNS. Another major barrier to improved treatment is that we cannot accurately identify children at risk of CNS relapse, or monitor response to treatment, due to a lack of sensitive biomarkers. A paradigm shift in treating the CNS is needed. The challenges are clear - we cannot measure CNS leukemic load, trials have been unable to establish the most effective CNS treatment regimens, and non-toxic approaches for relapsed, refractory, or intolerant patients are lacking. In this review we discuss these challenges and highlight research advances aiming to provide solutions. Unlocking the potential of risk-adapted non-toxic CNS-directed therapy requires; (1) discovery of robust diagnostic, prognostic and response biomarkers for CNS-leukemia, (2) identification of novel therapeutic targets combined with associated investment in drug development and early-phase trials and (3) engineering of immunotherapies to overcome the unique challenges of the CNS microenvironment. Fortunately, research into CNS-ALL is now making progress in addressing these unmet needs: biomarkers, such as CSF-flow cytometry, are now being tested in prospective trials, novel drugs are being tested in Phase I/II trials, and immunotherapies are increasingly available to patients with CNS relapses. The future is hopeful for improved management of the CNS over the next decade.
将有效的抗白血病药物递送到中枢神经系统(CNS)被认为是治愈儿童急性淋巴细胞白血病的关键。目前的中枢神经系统定向治疗包括具有良好中枢神经系统穿透性的全身治疗,并在 2-3 年内重复进行多达 26 次的鞘内治疗。这种方法可以预防大多数中枢神经系统复发,但与显著的短期和长期神经毒性相关。尽管进行了这种繁重的治疗,但自 20 世纪 60 年代以来,还没有新的药物被批准用于中枢神经系统白血病,当时可用的抗白血病药物非常有限,并且对中枢神经系统中白血病的存活机制也没有了解。另一个改善治疗的主要障碍是,由于缺乏敏感的生物标志物,我们无法准确识别有中枢神经系统复发风险的儿童,或监测对治疗的反应。需要对中枢神经系统的治疗进行范式转变。挑战很明显——我们无法测量中枢神经系统中的白血病负荷,试验也无法确定最有效的中枢神经系统治疗方案,而且缺乏针对复发、难治或不耐受患者的无毒方法。在这篇综述中,我们讨论了这些挑战,并强调了旨在提供解决方案的研究进展。要释放风险适应性无毒中枢神经系统定向治疗的潜力,需要:(1)发现用于中枢神经系统白血病的稳健诊断、预后和反应生物标志物,(2)识别新的治疗靶点,并结合相关药物开发和早期试验投资,以及(3)设计免疫疗法以克服中枢神经系统微环境的独特挑战。幸运的是,针对中枢神经系统 ALL 的研究现在正在解决这些未满足的需求方面取得进展:生物标志物,如脑脊液流式细胞术,现在正在前瞻性试验中进行测试,新的药物正在进行 I/II 期试验,免疫疗法越来越多地用于有中枢神经系统复发的患者。在未来十年内,对中枢神经系统的管理有望得到改善。