Wang Zihe, Tang Chuanhao, Liu Yi, Xu Bin, Qin Haifeng, Lei Yangyang, Gao Hongjun, He Kun, Liu Xiaoqing
Department of Lung Cancer, Affiliated Hospital of Academy of Military Medical Sciences, Beijing 100071, China.
Laboratory of Oncology, Affiliated Hospital of Academy of Military Medical Sciences, Beijing 100071, China.
Zhongguo Fei Ai Za Zhi. 2016 Sep 20;19(9):600-6. doi: 10.3779/j.issn.1009-3419.2016.09.08.
This study aimed at using matrix-assisted laser desorption ionization - time of flight mass spectrometer (matrix-assisted laser desorption ionization time-of-flight mass spectrometry, MALDI-TOF-MS) screening the difference serum peptides during epidermal growth factor tyrosine kinase inhibitors (EGFR-TKIs) treatment and exploring their significance of advanced NSCLC patients.
Collect 102 serum samples from 34 advanced NSCLC patients, which are before TKI treatment, best effect of treatment and after progession. Peptides were extracted from the samples and then detected by MALDI-TOF-MS system to get the mass spectra. The mass spectra data was analyzed by the ClinproToolTM software to identify the different serum peptides, and then analyzed the clinical significance of peptides.
Among the 34 patients who received TKI treatment, there were none evaluated as complete response (CR), 11 patients evaluated as PR and 23 patients evaluated as stable disease (SD), with the PFS was 8.0 months (95%CI: 6.6-11.2); overall survival (OS) was 11.4 months (95%CI: 10.6-16.5). After detected the serum from three different points of time, the result showed that they were totally different; 87 different peptide peaks were identified after analysis self-paired serum between the time of best effect and baseline, which included one statistically different [P<0.001, area under curve (AUC)≥0.9] peptide; 96 different peptide peaks were identified after analysis serum between the time of progression and baseline, which included 3 statistically different (P<0.001, AUC≥0.9) peptides; 115 different peptide peaks were identified after analysis serum between the time of progression and best effect, which included 4 statistically different (P<0.001, AUC≥0.9) peptides.
CONCLUSIONS: Theserum peptides of NSCLC patients in the process of TKI treatment are dynamic and the different peptides may be associated with treatment effect and disease progression. However, the features and clinical significance of different peptides need to be validated in the future. .
本研究旨在利用基质辅助激光解吸电离飞行时间质谱仪(MALDI-TOF-MS)筛查表皮生长因子酪氨酸激酶抑制剂(EGFR-TKIs)治疗期间晚期非小细胞肺癌(NSCLC)患者血清肽的差异,并探讨其意义。
收集34例晚期NSCLC患者在TKI治疗前、治疗最佳疗效时及疾病进展后的102份血清样本。从样本中提取肽段,然后用MALDI-TOF-MS系统进行检测以获得质谱图。用ClinproToolTM软件对质谱数据进行分析以鉴定不同的血清肽,进而分析肽段的临床意义。
在接受TKI治疗的34例患者中,无患者评估为完全缓解(CR),11例患者评估为部分缓解(PR),23例患者评估为疾病稳定(SD),无进展生存期(PFS)为8.0个月(95%CI:6.6-11.2);总生存期(OS)为11.4个月(95%CI:10.6-16.5)。检测三个不同时间点的血清后,结果显示它们完全不同;分析最佳疗效时与基线时的自身配对血清后,鉴定出87个不同的肽峰,其中包括1个具有统计学差异[P<0.001,曲线下面积(AUC)≥0.9]的肽段;分析疾病进展时与基线时的血清后,鉴定出96个不同的肽峰,其中包括3个具有统计学差异(P<0.001,AUC≥0.9)的肽段;分析疾病进展时与最佳疗效时的血清后,鉴定出115个不同的肽峰,其中包括4个具有统计学差异(P<0.001,AUC≥0.9)的肽段。
NSCLC患者在TKI治疗过程中的血清肽具有动态变化,不同的肽段可能与治疗效果和疾病进展相关。然而,不同肽段的特征及临床意义有待未来进一步验证。