Faculty of Science, University of Oradea, Oradea 410087, Romania; School of Physical Sciences, The University of Adelaide, SA 5005, Australia.
Phys Med. 2017 Oct;42:213-220. doi: 10.1016/j.ejmp.2017.02.013. Epub 2017 Feb 22.
Photons are widely used in radiotherapy and while they are low LET radiation, can still pose a risk in developing second malignant neoplasms (SMN). Due to the physics of photons that allow distribution of energy outside the target volume, out-of-field irradiation is an important component of SMN risk assessment. The epidemiological evidence supporting this risk should be augmented with radiobiological justifications for a better understanding of the underlying processes. There are several factors that impact second cancer risk which can be analysed from a radiobiological perspective: age at irradiation, type of irradiated tissue, irradiated volume, treatment technique, previous irradiation/radiological investigations. Age-dependence has a radiobiological foundation given by the higher radiosensitivity of children as compared to adult patients. However, in its 2013 report, UNSCEAR advises against generalisation of the effects of childhood radiation exposure, given the fact that these effects are strongly organ dependent. Furthermore, the age-dependent radiation sensitivity has a bimodal distribution, since aging cells present an increase in the oxidative stress, which can promote premalignant cells. Non-targeted effects such as radiation-induced genomic instability, bystander or abscopal effects could also impact on the risk of SMN. Recent studies show that beside the known cellular changes, bystander effects can be manifested through increased cell proliferation, which could be a culprit for SMN development. Furthermore, new evidence on the existence of tumour-specific cancer stem cells that are long-lived and more quiescent and radioresistant than non-stem cancer cells can raise questions about their association with SMN risk.
光子在放射治疗中被广泛应用,尽管它们属于低 LET 辐射,但仍有可能在形成第二恶性肿瘤(SMN)方面造成风险。由于光子的物理性质允许能量在靶体积之外分布,所以场外照射是 SMN 风险评估的一个重要组成部分。需要用放射生物学依据来支持支持这种风险的流行病学证据,以便更好地了解潜在过程。有几个影响第二癌症风险的因素可以从放射生物学的角度进行分析:照射时的年龄、受照射组织的类型、受照射体积、治疗技术、先前的照射/放射学研究。年龄依赖性具有放射生物学基础,因为与成年患者相比,儿童的放射敏感性更高。然而,UNSCEAR 在其 2013 年的报告中建议反对将儿童辐射暴露的影响一般化,因为这些影响强烈依赖于器官。此外,年龄依赖性的辐射敏感性呈双峰分布,因为老化细胞的氧化应激增加,这可能促进癌前细胞。非靶向效应,如辐射诱导的基因组不稳定性、旁观者或远隔效应,也可能影响 SMN 的风险。最近的研究表明,除了已知的细胞变化之外,旁观者效应可以通过增加细胞增殖来表现出来,这可能是 SMN 发展的罪魁祸首。此外,关于存在寿命长、更静止和放射抗性比非干细胞更强的肿瘤特异性癌症干细胞的新证据,可能会引发关于它们与 SMN 风险关联的问题。