1 School of Medicine and Life Sciences, University of Jinan-Shandong Academy of Medical Sciences , Jinan, China .
2 Shandong Provincial Key Laboratory of Radiation Oncology, Cancer Research Center, Shandong Cancer Hospital Affiliated to Shandong University , Shandong Academy of Medical Sciences, Jinan, China .
DNA Cell Biol. 2018 Nov;37(11):903-908. doi: 10.1089/dna.2018.4337. Epub 2018 Oct 2.
Gefitinib is currently one of the mostly used epidermal growth factor receptor tyrosine kinase inhibitors (EGFR-TKIs) recommended for treating nonsmall cell lung cancer. However, drug resistance is observed among the majority of patients after initial treatment. Factors that predict treatment prognosis and drug resistance to EGFR-TKIs remain elusive. The objective of this study is to investigate whether leukocyte relative telomere length (RTL) can be used as a prognostic biomarker of EGFR-TKIs therapy. In this study, 369 patients with stage IIIB or IV lung adenocarcinoma were recruited and treated with gefitinib as first-line monotherapy. Leukocyte RTL of each patient was measured using quantitative polymerase chain reaction protocol and calculated according to Cawthon's formula. Finally, we examined the association between leukocyte RTL and prognosis or drug resistance of advanced lung adenocarcinoma to gefitinib treatment. Our results indicated that compared with long RTL, short leukocyte RTL was significantly associated with poor prognosis in all patients after gefitinib treatment (overall survival [OS]: 12.9 months vs. 17.8 months, p = 1.2 × 10; progression-free survival: 7.8 months vs. 13.0 months, p = 0.043). In addition, statistically significant association between short leukocyte RTL and short OS still existed among the EGFR mutant patients (hazards ratio [HR] = 1.65, 95% confidence interval [CI] = 1.28-2.12; p = 0.006). Besides EGFR mutation status, short RTL also contributed to remarkably elevated risk of gefitinib primary resistance (HR = 1.50, 95% CI = 1.05-2.15, p = 0.027). Our results highlight the clinical potential of leukocyte RTL as a novel biomarker in advanced lung adenocarcinoma treated with EGFR-TKIs.
吉非替尼是目前推荐用于治疗非小细胞肺癌的表皮生长因子受体酪氨酸激酶抑制剂(EGFR-TKIs)之一。然而,大多数患者在初始治疗后都会出现耐药性。预测 EGFR-TKIs 治疗预后和耐药性的因素仍难以捉摸。本研究旨在探讨白细胞相对端粒长度(RTL)是否可用作 EGFR-TKIs 治疗的预后生物标志物。在这项研究中,招募了 369 名 IIIB 或 IV 期肺腺癌患者,并使用吉非替尼作为一线单药治疗。使用定量聚合酶链反应方案测量每位患者的白细胞 RTL,并根据 Cawthon 公式进行计算。最后,我们检查了白细胞 RTL 与吉非替尼治疗晚期肺腺癌的预后或耐药性之间的关联。我们的研究结果表明,与长 RTL 相比,短白细胞 RTL 与吉非替尼治疗后所有患者的预后不良显著相关(总生存期 [OS]:12.9 个月比 17.8 个月,p=1.2×10;无进展生存期:7.8 个月比 13.0 个月,p=0.043)。此外,在 EGFR 突变患者中,短白细胞 RTL 与短 OS 之间仍然存在统计学显著关联(风险比 [HR]=1.65,95%置信区间 [CI]=1.28-2.12;p=0.006)。除了 EGFR 突变状态外,短 RTL 还导致吉非替尼原发性耐药的风险显著增加(HR=1.50,95%CI=1.05-2.15,p=0.027)。我们的研究结果强调了白细胞 RTL 作为 EGFR-TKIs 治疗晚期肺腺癌的新型生物标志物的临床潜力。