a Clinical Pneumology Ward , Medical University of Lodz , Lodz , Poland.
b Department of Clinical Physiology , Medical University of Lodz , Lodz , Poland.
Redox Rep. 2017 Nov;22(6):308-314. doi: 10.1080/13510002.2016.1229885. Epub 2016 Sep 9.
Reactive oxygen species, which are implicated in the process of carcinogenesis, are also responsible for cell death during chemotherapy (CHT). Therefore, the aim of the study was to evaluate exhaled HO levels in non-small cell lung cancer (NSCLC) patients before and after CHT.
Thirty patients (age 61.3 ± 9.3 years) with advanced NSCLC (stage IIIB-IV) and 15 age-matched healthy cigarette smokers were enrolled into the study. Patients received four cycles of cisplatin or carboplatin with vinorelbine every three weeks. Before and after the first, second, and fourth cycle, the concentration of HO in exhaled breath condensate was measured with respect to treatment response.
At the baseline, NSCLC patients exhaled 3.8 times more HO than the control group (0.49 ± 0.14 vs. 0.13 ± 0.03 µmol/L, P < 0.05); this difference persisted throughout the study. CHT had no noticeable effect on exhaled HO levels independent of the treatment response (partial remission vs. progressive disease). Pre- and post-CHT cycles of HO levels generally correlated positively.
The study demonstrated the occurrence of oxidative stress in the airways of advanced NSCLC patients. Exhaled HO level was not affected by CHT and independent of treatment results and changes in the number of circulating neutrophils.
活性氧参与致癌过程,也是化疗(CHT)期间细胞死亡的原因。因此,本研究旨在评估非小细胞肺癌(NSCLC)患者 CHT 前后呼出气 HO 水平。
30 名(年龄 61.3±9.3 岁)晚期 NSCLC(IIIb-IV 期)患者和 15 名年龄匹配的健康吸烟人群纳入本研究。患者接受每 3 周一次的顺铂或卡铂联合长春瑞滨 4 个周期的治疗。在每个周期(第 1、2、4 周期)治疗前和治疗后,评估 HO 浓度与治疗反应的相关性。
在基线时,NSCLC 患者呼出气 HO 浓度比对照组高 3.8 倍(0.49±0.14 vs. 0.13±0.03 μmol/L,P<0.05);这种差异在整个研究期间持续存在。CHT 对呼出气 HO 水平无明显影响,与治疗反应(部分缓解与疾病进展)无关。HO 水平在 CHT 前后周期之间通常呈正相关。
本研究表明晚期 NSCLC 患者气道发生氧化应激。HO 水平不受 CHT 影响,与治疗结果以及循环中性粒细胞数量的变化无关。