Lee Seung Hyeun, Choi Sue In, Lee Ji Sung, Kim Chul Hwan, Jung Won Jai, Lee Eun Joo, Min Kyung Hoon, Hur Gyu Young, Lee Seung Heon, Lee Sung Yong, Kim Je Hyeong, Lee Sang Yeub, Shin Chol, Shim Jae Jeong, Kang Kyung Ho, In Kwang Ho
Department of Internal Medicine, Kyung Hee University School of Medicine, Seoul, Korea.
Division of Respiratory and Critical Care Medicine, Department of Internal Medicine, Korea University College of Medicine, Seoul, Korea.
Cancer Res Treat. 2017 Jan;49(1):141-149. doi: 10.4143/crt.2016.133. Epub 2016 May 18.
Reactive oxygen species modulator 1 (Romo1) is a key mediator of intracellular reactive oxygen species production. However, examination of the clinical usefulness of Romo1 in cancers has been limited. We evaluated the association of Romo1 expression with clinical outcomes in advanced non-small cell lung cancer (NSCLC) patients treated with platinum-based chemotherapy.
Romo1 expression in tumor tissue was examined by immunohistochemistry and evaluated by histological score. Survival analyses were performed according to Romo1 expression and the association between Romo1 expression and clinical parameters was evaluated.
A total of 88 tumor specimens were analyzed. Significantly shorter median progression-free survival (PFS) was observed in the high Romo1 group compared with the low Romo1 group (4.5 months vs. 9.8 months, p < 0.001), and the median overall survival (OS) of the high Romo1 group was also significantly shorter than that of the low Romo1 group (8.4 months vs. 15.5 months, p < 0.001). Results of multivariate analyses showed significant association of high Romo1 expression with both poor PFS (hazard ratio [HR], 2.75; 95% confidence interval [CI], 1.71 to 4.44) and poor OS (HR, 3.99; 95% CI, 2.36 to 6.74). Results of the subgroup analysis showed a similar association regardless of tumor histology. Romo1 expression showed no association with any clinical parameter including age, sex, smoking status, stage, differentiation, or tumor histology.
Romo1 overexpression was associated with poor response to treatment and shorter survival in advanced NSCLC patients treated with platinum-based chemotherapy. Romo1 could be a potential adverse predictive marker in this setting.
活性氧调节剂1(Romo1)是细胞内活性氧产生的关键介质。然而,Romo1在癌症临床应用方面的研究有限。我们评估了Romo1表达与接受铂类化疗的晚期非小细胞肺癌(NSCLC)患者临床结局之间的关联。
采用免疫组织化学法检测肿瘤组织中Romo1的表达,并通过组织学评分进行评估。根据Romo1表达进行生存分析,并评估Romo1表达与临床参数之间的关联。
共分析了88个肿瘤标本。与低Romo1组相比(4.5个月对9.8个月,p<0.001),高Romo1组的中位无进展生存期(PFS)显著缩短,高Romo1组的中位总生存期(OS)也显著短于低Romo1组(8.4个月对15.5个月,p<0.001)。多因素分析结果显示,高Romo1表达与较差的PFS(风险比[HR],2.75;95%置信区间[CI],1.71至4.44)和较差的OS(HR,3.99;95%CI,2.36至6.74)均显著相关。亚组分析结果显示,无论肿瘤组织学类型如何,均存在类似的关联。Romo1表达与任何临床参数(包括年龄、性别、吸烟状况、分期、分化程度或肿瘤组织学类型)均无关联。
在接受铂类化疗的晚期NSCLC患者中,Romo1过表达与治疗反应差和生存期短相关。在这种情况下,Romo1可能是一个潜在的不良预测标志物。