Po Joseph W, Ma Yafeng, Balakrishnar Bavanthi, Brungs Daniel, Azimi Farhad, Cooper Adam, Saricilar Erin, Murthy Vinay, de Souza Paul, Becker Therese M
Centre for Circulating Tumour Cell Diagnostics & Research at the Ingham Institute for Applied Medical Research, Liverpool, NSW, Australia.
Centre for Oncology Education and Research Translation (CONCERT), Liverpool, NSW, Australia.
Methods Mol Biol. 2021;2265:223-233. doi: 10.1007/978-1-0716-1205-7_17.
The advent of personalized medicines targeting cell signaling pathways has radically improved melanoma patient outcomes. More recently, immune-modulating therapies disrupting the PD-1/PD-L1 axis have become a powerful tool in the treatment of a range of melanoma, showing a profound improvement in the overall survival outcomes. However, immune checkpoint inhibitors (ICIs) are associated with considerable toxicities and appear to only be efficacious in a subset of melanoma patients. Therefore, there is an urgent need to identify biomarkers that can determine if patients will or will not respond to ICI therapy. Here, we describe an optimized method for analyzing PD-L1 expression on circulating melanoma cells following immunomagnetic enrichment from patient blood samples.
针对细胞信号通路的个性化药物的出现,从根本上改善了黑色素瘤患者的治疗效果。最近,破坏PD-1/PD-L1轴的免疫调节疗法已成为治疗一系列黑色素瘤的有力工具,显著改善了总体生存结果。然而,免疫检查点抑制剂(ICI)具有相当大的毒性,而且似乎仅对一部分黑色素瘤患者有效。因此,迫切需要确定能够判定患者是否会对ICI治疗产生反应的生物标志物。在此,我们描述了一种优化方法,用于分析从患者血液样本中经免疫磁珠富集后的循环黑色素瘤细胞上的PD-L1表达。