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Prediction of outcome of non-small cell lung cancer patients treated with chemotherapy and bortezomib by time-course MALDI-TOF-MS serum peptide profiling

机译:时程MALDI-TOF-MS血清肽谱分析预测化疗和硼替佐米治疗的非小细胞肺癌患者的预后

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Background Only a minority of patients with advanced non-small cell lung cancer (NSCLC) benefit from chemotherapy. Serum peptide profiling of NSCLC patients was performed to investigate patterns associated with treatment outcome. Using magnetic bead-assisted serum peptide capture coupled to matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF-MS), serum peptide mass profiles of 27 NSCLC patients treated with cisplatin-gemcitabine chemotherapy and bortezomib were obtained. Support vector machine-based algorithms to predict clinical outcome were established based on differential pre-treatment peptide profiles and dynamic changes in peptide abundance during treatment. Results A 6-peptide ion signature distinguished with 82% accuracy, sensitivity and specificity patients with a relatively short vs. long progression-free survival (PFS) upon treatment. Prediction of long PFS was associated with longer overall survival. Inclusion of 7 peptide ions showing differential changes in abundance during treatment led to a 13-peptide ion signature with 86% accuracy at 100% sensitivity and 73% specificity. A 5-peptide ion signature could separate patients with a partial response vs. non-responders with 89% accuracy at 100% sensitivity and 83% specificity. Differential peptide profiles were also found when comparing the NSCLC serum profiles to those from cancer-free control subjects. Conclusion This study shows that serum peptidome profiling using MALDI-TOF-MS coupled to pattern diagnostics may aid in prediction of treatment outcome of advanced NSCLC patients treated with chemotherapy.
机译:背景技术仅少数患有晚期非小细胞肺癌(NSCLC)的患者可从化疗中受益。对NSCLC患者进行血清肽谱分析,以研究与治疗结果相关的模式。使用磁珠辅助血清肽捕获结合基质辅助激光解吸/电离飞行时间质谱(MALDI-TOF-MS),获得了27例接受顺铂-吉西他滨化疗和硼替佐米治疗的NSCLC患者的血清肽质量谱。基于支持向量机的算法预测临床结果,是基于不同的预处理肽谱和治疗过程中肽丰度的动态变化而建立的。结果6肽离子标记具有82%的准确性,敏感性和特异性,在治疗后相对无进展生存期(PFS)相对较长。长期PFS的预测与更长的总生存期有关。包含7个在处理过程中丰度差异变化的肽离子导致13肽离子签名,在100%灵敏度和73%特异性下的准确度为86%。 5肽离子标记可以以100%的敏感性和83%的特异性将有部分反应的患者与无反应者分开,准确率为89%。当将NSCLC血清谱与无癌对照受试者的血清谱进行比较时,也发现了差异肽谱。结论这项研究表明,使用MALDI-TOF-MS结合模式诊断进行血清肽组分析可能有助于预测晚期NSCLC化疗患者的治疗结果。

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