Singh Jagtar, Sohal Sukhwinder Singh, Lim Aijye, Duncan Henry, Thachil Thanuja, De Ieso Paolo
College of Health and Human Sciences, Charles Darwin University, Darwin, Northern Territory, Australia.
School of Health Sciences, University of Tasmania, Launceston, Tasmania, Australia.
Ann Transl Med. 2019 Jun;7(11):245. doi: 10.21037/atm.2019.05.31.
Prostate cancer (PC) is a common cancer (excluding non-melanoma skin cancer) in men in many parts of the world, although incidence and mortality rates vary significantly by population. In current medical practice, prognostic markers for PC include the presenting serum prostate-specific antigen (PSA) level, tumour Gleason score (GS) and clinical tumour stage. However, existing pre-treatment factors cannot be used to predict acute radiotherapy (RT)-induced toxicity. Therefore, new protein biomarkers are required in RT oncology to improve decision-making, treatment and therapy monitoring for PC patients. The aim of this systematic review is to the update potential research to address the difference in cytokine expression and their association with RT-induced toxicity and clinical outcomes. Studies were collected after searching three electronic databases: PubMed, Medline, and Google Scholar. An additional search was carried out through cross-check on a bibliography of selected articles. After the selection process made by two of the authors, 19 articles met the inclusion criteria and were included in the systematic review. Results from previous studies identified elevated levels of cytokines have been reported in several types of cancers and have sometimes correlated with disease progression or prognosis. Elevated levels of cytokine were noticed after immediate exposure to RT and their association with RT-induced acute/late toxicity of PC patients. Moreover, above studies also identified overexpression of cytokines on tumour biopsies and correlation with shortening cancer-specific survival and biochemical recurrence. Thus, altered levels of cytokine might be predictive biomarkers for RT-induced and clinical outcomes of PC patients.
前列腺癌(PC)是世界上许多地区男性常见的癌症(不包括非黑色素瘤皮肤癌),尽管发病率和死亡率因人群而异。在当前的医学实践中,PC的预后标志物包括就诊时的血清前列腺特异性抗原(PSA)水平、肿瘤Gleason评分(GS)和临床肿瘤分期。然而,现有的治疗前因素无法用于预测急性放疗(RT)引起的毒性。因此,放射肿瘤学需要新的蛋白质生物标志物来改善PC患者的决策制定、治疗和治疗监测。本系统评价的目的是更新潜在研究,以解决细胞因子表达的差异及其与RT诱导的毒性和临床结果的关联。在检索三个电子数据库(PubMed、Medline和谷歌学术)后收集了相关研究。通过对所选文章的参考文献进行交叉核对进行了额外的搜索。在两位作者进行筛选后,19篇文章符合纳入标准并被纳入系统评价。先前研究的结果表明,在几种类型的癌症中都报告了细胞因子水平升高,并且有时与疾病进展或预后相关。在立即接受放疗后注意到细胞因子水平升高及其与PC患者放疗诱导的急性/晚期毒性的关联。此外,上述研究还确定了肿瘤活检中细胞因子的过表达以及与缩短癌症特异性生存期和生化复发的相关性。因此,细胞因子水平的改变可能是PC患者放疗诱导的毒性和临床结果的预测生物标志物。