Fok Matthew, Hill Rhianna, Fowler Hayley, Clifford Rachael, Kler Aaron, Uzzi-Daniel Jayanma, Rocha Sonia, Grundy Gabrielle, Parsons Jason, Vimalachandran Dale
Institute of Systems, Molecular and Integrative Biology University of Liverpool, UK.
Institute of Cancer and Genomic Sciences, University of Birmingham, UK.
Clin Transl Radiat Oncol. 2023 Oct 28;44:100695. doi: 10.1016/j.ctro.2023.100695. eCollection 2024 Jan.
Neoadjuvant radiotherapy is successfully used in rectal cancer to improve overall survival. However, treatment response is both unpredictable and variable. There is strong evidence to show that the phenomenon of tumour hypoxia is associated with radioresistance, however the mechanism(s) behind this are poorly understood. Consequently, there have only been a small number of studies evaluating methods targeting hypoxia-induced radioresistance. The purpose of this systematic review is to evaluate the potential effectiveness of targeting hypoxia-induced radioresistance in rectal cancer and provide recommendations for future research in this area.
A comprehensive literature search was performed following the PRISMA guidelines. This study was registered on the Prospero database (CRD42023441983).
Eight articles met the inclusion criteria. All studies identified were or studies, there were no clinical trials. Of the 8 studies identified, 5 assessed the efficacy of drugs which directly or indirectly targeted hypoxia and three that identified potential targets. There was conflicting evidence for the use of metformin to overcome hypoxia induced radioresistance. Vorinostat, atovaquone, and evofosfamide showed promising preclinical evidence that they can overcome hypoxia-induced radioresistance.
The importance of investigating hypoxia-induced radioresistance in rectal cancer is crucial. However, to date, only a small number of preclinical studies exist evaluating this phenomenon. This systematic review highlights the importance of further research to fully understand the mechanism behind this radioresistance. There are promising targets identified in this systematic review however, substantially more pre-clinical and clinical research as a priority for future research is needed.
新辅助放疗已成功应用于直肠癌以提高总生存率。然而,治疗反应既不可预测又存在差异。有强有力的证据表明肿瘤缺氧现象与放射抗性相关,但其背后的机制仍知之甚少。因此,仅有少数研究评估针对缺氧诱导的放射抗性的方法。本系统评价的目的是评估针对直肠癌中缺氧诱导的放射抗性的潜在有效性,并为该领域的未来研究提供建议。
按照PRISMA指南进行全面的文献检索。本研究已在Prospero数据库(CRD42023441983)注册。
8篇文章符合纳入标准。所有纳入的研究均为观察性或实验性研究,无临床试验。在确定的8项研究中,5项评估了直接或间接靶向缺氧的药物的疗效,3项确定了潜在靶点。关于使用二甲双胍克服缺氧诱导的放射抗性存在相互矛盾的证据。伏立诺他、阿托伐醌和依沃福酰胺显示出有前景的临床前证据,表明它们可以克服缺氧诱导的放射抗性。
研究直肠癌中缺氧诱导的放射抗性的重要性至关重要。然而,迄今为止,仅有少数临床前研究评估这一现象。本系统评价强调了进一步研究以充分了解这种放射抗性背后机制的重要性。本系统评价确定了有前景的靶点,然而,作为未来研究的优先事项,需要更多的临床前和临床研究。