Hockings Helen, Lakatos Eszter, Huang Weini, Mossner Maximilian, Khan Mohammed A, Bakali Nikolina, McDermott Jacqueline, Smith Kane, Baker Ann-Marie, Graham Trevor A, Lockley Michelle
Queen Mary University of London, LONDON, United Kingdom.
Institute of Cancer Research, United Kingdom.
Cancer Res. 2025 Apr 29. doi: 10.1158/0008-5472.CAN-25-0351.
Drug resistance results in poor outcomes for cancer patients. Adaptive therapy is a potential strategy to address drug resistance that exploits competitive interactions between sensitive and resistant subclones. Here, we showed that adapting carboplatin dose according to tumor response (adaptive therapy) significantly prolonged survival of murine ovarian cancer models compared to standard carboplatin dosing, without increasing mean daily drug dose or toxicity. Platinum resistant ovarian cancer cells exhibited diminished fitness when drug was absent in vitro and in vivo, which caused selective decline of resistant populations due to reduced proliferation and increased apoptosis. Conversely fitter, sensitive cells re-grew when drug was withdrawn. Using a bioinformatics pipeline that exploits copy number changes to quantify the emergence of treatment resistance, analysis of cell-free DNA obtained longitudinally from ovarian cancer patients during treatment showed subclonal selection through therapy, and measurements of resistant population growth correlated strongly with disease burden. These preclinical findings pave the way for future clinical testing of personalized adaptive therapy regimens tailored to the evolution of carboplatin resistance in individual ovarian cancer patients.
耐药性导致癌症患者预后不良。适应性疗法是一种应对耐药性的潜在策略,它利用敏感和耐药亚克隆之间的竞争性相互作用。在此,我们表明,与标准卡铂给药相比,根据肿瘤反应调整卡铂剂量(适应性疗法)显著延长了小鼠卵巢癌模型的生存期,且未增加日均药物剂量或毒性。铂耐药卵巢癌细胞在体外和体内无药物时表现出适应性降低,这导致耐药群体因增殖减少和凋亡增加而选择性减少。相反,当撤药时,适应性更强的敏感细胞重新生长。使用一种利用拷贝数变化来量化治疗耐药性出现的生物信息学流程,对卵巢癌患者治疗期间纵向获取的游离DNA进行分析,结果显示治疗过程中存在亚克隆选择,耐药群体生长的测量与疾病负担密切相关。这些临床前研究结果为未来针对个体卵巢癌患者卡铂耐药演变量身定制的个性化适应性治疗方案的临床试验铺平了道路。