Li Jian, Hu Yi-Ming, Du Yong-Jie, Zhu Li-Rong, Qian Hai, Wu Yan, Shi Wei-Lin
Department of Pulmonary Medicine, Affiliated Hospital of Jiangsu University, 438 North Jiefang Street, Zhenjiang 212001, China.
BMC Cancer. 2014 Nov 19;14:848. doi: 10.1186/1471-2407-14-848.
Gefitinib, an EGFR-tyrosine kinase inhibitor, significantly improve prognosis in patients with advanced non-small cell lung cancer (NSCLC). The aim of this study was to evaluate the usefulness of MUC1 and vascular endothelial growth factor (VEGF) mRNA expression in peripheral blood as means of predicting benefit from gefitinib therapy in NSCLC patients.
MUC1 and VEGF mRNA expressions were detected in peripheral blood of 66 patients with advanced NSCLC before (B0) and 4 weeks after treatment (B4w) with gefitinib, using real-time quantitative-PCR assay. Correlations between blood MUC1 and VEGF mRNA expression at B0 and B4w and the response to gefitinib treatment and survival were analyzed.
Blood levels of MUC1 and VEGF mRNA at B0 and at B4w were significantly higher in patients with progressive disease than in those with partial response and stable disease. Furthermore, blood MUC1 and VEGF mRNA positivity at two time points were strongly associated with shorter progression-free survival (PFS) and overall survival (OS) (P = 0.005 and P = 0.008 at B0, and P < 0.001 and P = 0.001 at B4w, respectively, for MUC1; P = 0.004 and P = 0.009 at B0, and P = 0.001 and P < 0.001 at B4w, respectively, for VEGF). Multivariate analyses demonstrated that blood MUC1 and VEGF mRNA positivity at B0 and B4w were independent factors for predicting worse PFS and OS.
MUC1 and VEGF mRNA positivity in blood seem to be indicators of unfavorable response and poor PFS and OS in patients with advanced NSCLC treated with gefitinib and may be promising noninvasive and repeatable markers for predicting efficacy of gefitinib treatment.
吉非替尼是一种表皮生长因子受体酪氨酸激酶抑制剂(EGFR - TKI),可显著改善晚期非小细胞肺癌(NSCLC)患者的预后。本研究旨在评估外周血中粘蛋白1(MUC1)和血管内皮生长因子(VEGF)mRNA表达作为预测NSCLC患者从吉非替尼治疗中获益的手段的有效性。
采用实时定量聚合酶链反应(real - time quantitative - PCR)检测66例晚期NSCLC患者在接受吉非替尼治疗前(B0)和治疗4周后(B4w)外周血中MUC1和VEGF mRNA的表达。分析B0和B4w时血液中MUC1和VEGF mRNA表达与吉非替尼治疗反应及生存情况之间的相关性。
疾病进展患者在B0和B4w时血液中MUC1和VEGF mRNA水平显著高于部分缓解和病情稳定的患者。此外,两个时间点血液中MUC1和VEGF mRNA阳性与较短的无进展生存期(PFS)和总生存期(OS)密切相关(MUC1在B0时P = 0.005和P = 0.008,在B4w时P < 0.001和P = 0.001;VEGF在B0时P = 0.004和P = 0.009,在B4w时P = 0.001和P < 0.001)。多因素分析表明,B0和B4w时血液中MUC1和VEGF mRNA阳性是预测PFS和OS较差的独立因素。
血液中MUC1和VEGF mRNA阳性似乎是接受吉非替尼治疗的晚期NSCLC患者不良反应及PFS和OS较差的指标,可能是预测吉非替尼治疗疗效的有前景的非侵入性和可重复性标志物。