Health Science Graduate Program, School of Health Sciences, University of Brasilia, Brasília, DF, Brazil.
Nursing Department, School of Health Sciences, University of Brasilia, Brasília, DF, Brazil.
Strahlenther Onkol. 2024 Jul;200(7):568-582. doi: 10.1007/s00066-024-02237-3. Epub 2024 Apr 26.
To identify potential Single Nucleotide Polymorphisms (SNPs) of susceptibility for the development of acute radiation dermatitis in head and neck cancer patients, and also to verify the association between SNPs and the severity of RD.
This systematic review was reported according to the PRISMA guideline. The proportion meta-analysis was performed to identify the prevalence of genetic markers by geographical region and radiation dermatitis severity. The meta-analysis was performed to verify the association between genetic markers and RD severity. The certainty of the evidence was assessed by GRADE.
Thirteen studies were included. The most prevalent SNPs were XRCC3 (rs861639) (36%), TGFβ1 (rs1800469) (35%), and RAD51 (rs1801321) (34%). There are prevalence studies in Europe and Asia, with a similar prevalence for all SNPs (29-40%). The prevalence was higher in patients who developed radiation dermatitis ≤2 for any subtype of genes (75-76%). No SNP showed a statistically significant association with very low certainty of evidence.
The most prevalent SNPs may be predictors of acute RD. The analysis of SNP before starting radiation therapy may be a promising method to predict the risk of developing radiation dermatitis and allow radiosensitive patients to have a customized treatment. This current review provides new research directions.
鉴定头颈部癌症患者发生急性放射性皮炎的易感性单核苷酸多态性(SNP),并验证 SNP 与 RD 严重程度的相关性。
本系统评价按照 PRISMA 指南进行报告。采用比例荟萃分析确定遗传标记在地理区域和放射性皮炎严重程度上的流行率。采用荟萃分析验证遗传标记与 RD 严重程度的相关性。采用 GRADE 评估证据的确定性。
纳入 13 项研究。最常见的 SNP 是 XRCC3(rs861639)(36%)、TGFβ1(rs1800469)(35%)和 RAD51(rs1801321)(34%)。有欧洲和亚洲的流行率研究,所有 SNP 的流行率相似(29-40%)。在任何类型基因的放射性皮炎≤2 患者中,SNP 的流行率更高(75-76%)。没有 SNP 表现出与非常低确定性证据的统计学显著关联。
最常见的 SNP 可能是急性 RD 的预测因子。在开始放射治疗前分析 SNP 可能是预测放射性皮炎发生风险的一种很有前途的方法,并允许对敏感的患者进行个性化治疗。本综述提供了新的研究方向。