Wilshire Oncology Medical Group-US Oncology, La Verne, California 91750, USA.
Cancer Res. 2012 Aug 15;72(16):3901-5. doi: 10.1158/0008-5472.CAN-12-0681. Epub 2012 Aug 3.
A drug-induced apoptosis assay, termed the microculture-kinetic (MiCK) assay, has been developed. Blinded clinical trials have shown higher response rates and longer survival in groups of patients with acute myelocytic leukemia and epithelial ovarian cancer who have been treated with drugs that show high apoptosis in the MiCK assay. Unblinded clinical trials in multiple tumor types have shown that the assay will be used frequently by clinicians to determine treatment, and when used, results in higher response rates, longer times to relapse, and longer survivals. Model economic analyses suggest possible cost savings in clinical use based on increased generic drug use and single-agent substitution for combination therapies. Two initial studies with drugs in development are promising. The assay may help reduce costs and speed time to drug approval. Correlative studies with molecular biomarkers are planned. This assay may have a role both in personalized clinical therapy and in more efficient drug development.
一种药物诱导细胞凋亡检测方法,称为微量培养动力学(MiCK)检测法,已经建立。在接受 MiCK 检测中显示高凋亡的药物治疗的急性髓性白血病和上皮性卵巢癌患者中,盲法临床试验显示出更高的反应率和更长的生存时间。在多种肿瘤类型的非盲法临床试验中表明,该检测方法将被临床医生频繁用于确定治疗方法,并且在使用时,可提高反应率,延缓复发时间和延长生存时间。基于增加仿制药的使用和单一药物替代联合疗法的模型经济分析表明,在临床应用中可能会节省成本。两种正在开发中的药物的初步研究结果令人鼓舞。该检测方法可能有助于降低成本并加快药物审批时间。计划进行与分子生物标志物的相关性研究。该检测方法在个性化临床治疗和更有效的药物开发中可能都有一定作用。