Kong Moonkyoo, Sung Ji-Youn, Lee Seung Hyeun
Division of Lung & Head and Neck Oncology, Department of Radiation Oncology, Kyung Hee University Medical Center, Kyung Hee University School of Medicine, Seoul, Republic of Korea.
Department of Pathology, Kyung Hee University Medical Center, Kyung Hee University School of Medicine, Seoul, Republic of Korea.
Onco Targets Ther. 2019 Oct 9;12:8263-8273. doi: 10.2147/OTT.S217514. eCollection 2019.
Reactive oxygen species modulator 1 (ROMO1) is a novel protein regulating intracellular reactive oxygen species production. Although increased ROMO1 expression has been associated with poor clinical outcomes in several human malignancies, the clinical implication of this protein in a radiotherapy setting has never been explored. The aim of this study was to investigate whether ROMO1 expression is associated with survival in lung cancer patients who received radiotherapy.
ROMO1 protein expression was evaluated immunohistochemically using histologic score (H-score) in 49 tumor tissues from stage III non-small cell lung cancer (NSCLC) patients treated with definitive radiotherapy. We performed survival analyses according to various clinicopathological parameters including ROMO1 expression.
ROMO1 expression was not associated with any clinicopathological parameter of age, sex, smoking status, stage, or histological subtype. Multivariate analyses showed that high ROMO1 expression was independently associated with worse progression-free survival (hazard ratio [HR] = 1.87, 95% confidence interval [CI]: 1.02-4.23) and with worse overall survival (HR = 2.79, 95% CI:1.13-6.87). In addition, high ROMO1 expression was independently associated with shorter time to loco-regional recurrence (HR=2.71, 95% CI:1.04-6.28) but was not associated with time to distant metastasis.
ROMO1 overexpression was associated with early loco-regional recurrence and poor survival outcomes in stage III NSCLC treated with definitive radiotherapy. Our exploratory results provide a basis for further large-scale studies to validate whether ROMO1 could be a prognostic marker in this setting.
活性氧调节剂1(ROMO1)是一种调节细胞内活性氧产生的新型蛋白质。尽管在几种人类恶性肿瘤中,ROMO1表达增加与不良临床结局相关,但该蛋白在放疗环境中的临床意义从未被探讨过。本研究的目的是调查ROMO1表达是否与接受放疗的肺癌患者的生存相关。
使用组织学评分(H评分)对49例接受根治性放疗的III期非小细胞肺癌(NSCLC)患者的肿瘤组织进行免疫组织化学评估,以检测ROMO1蛋白表达。我们根据包括ROMO1表达在内的各种临床病理参数进行生存分析。
ROMO1表达与年龄、性别、吸烟状态、分期或组织学亚型等任何临床病理参数均无关联。多变量分析显示,ROMO1高表达与无进展生存期较差独立相关(风险比[HR]=1.87,95%置信区间[CI]:1.02-4.23),与总生存期较差也独立相关(HR=2.79,95%CI:1.13-6.87)。此外,ROMO1高表达与局部区域复发时间较短独立相关(HR=2.71,95%CI:1.04-6.28),但与远处转移时间无关。
在接受根治性放疗的III期NSCLC中,ROMO1过表达与早期局部区域复发和不良生存结局相关。我们的探索性结果为进一步的大规模研究提供了基础,以验证ROMO1是否可作为该情况下的预后标志物。