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首页> 外文期刊>International Journal of Radiation Oncology, Biology, Physics >Acute normal tissue reactions in head-and-neck cancer patients treated with IMRT: influence of dose and association with genetic polymorphisms in DNA DSB repair genes.
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Acute normal tissue reactions in head-and-neck cancer patients treated with IMRT: influence of dose and association with genetic polymorphisms in DNA DSB repair genes.

机译:IMRT治疗的头颈癌患者的急性正常组织反应:剂量的影响以及与DNA DSB修复基因中遗传多态性的关系。

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PURPOSE: To investigate the association between dose-related parameters and polymorphisms in DNA DSB repair genes XRCC3 (c.-1843A>G, c.562-14A>G, c.722C>T), Rad51 (c.-3429G>C, c.-3392G>T), Lig4 (c.26C>T, c.1704T>C), Ku70 (c.-1310C>G), and Ku80 (c.2110-2408G>A) and the occurrence of acute reactions after radiotherapy. MATERIALS AND METHODS: The study population consisted of 88 intensity-modulated radiation therapy (IMRT)-treated head-and-neck cancer patients. Mucositis, dermatitis, and dysphagia were scored using the Common Terminology Criteria (CTC) for Adverse Events v.3.0 scale. The population was divided into a CTC0-2 and CTC3+ group for the analysis of each acute effect. The influence of the dose on critical structures was analyzed using dose-volume histograms. Genotypes were determined by polymerase chain reaction (PCR) combined with restriction fragment length polymorphism or PCR-single base extension assays. RESULTS: The mean dose (D(mean)) to the oral cavity and constrictor pharyngeus (PC) muscles was significantly associated with the development of mucositis and dysphagia, respectively. These parameters were considered confounding factors in the radiogenomics analyses. The XRCC3c.722CT/TT and Ku70c.-1310CG/GG genotypes were significantly associated with the development of severe dysphagia (CTC3+). No association was found between the investigated polymorphisms and the development of mucositis or dermatitis. A risk analysis model for severe dysphagia, which was developed based on the XRCC3c.722CT/TT and Ku70c.-1310CG/GG genotypes and the PC dose, showed a sensitivity of 78.6% and a specificity of 77.6%. CONCLUSIONS: The XRCC3c.722C>T and Ku70c.-1310C>G polymorphisms as well as the D(mean) to the PC muscles were highly associated with the development of severe dysphagia after IMRT. The prediction model developed using these parameters showed a high sensitivity and specificity.
机译:目的:研究剂量相关参数与DNA DSB修复基因XRCC3(c.-1843A> G,c.562-14A> G,c.722C> T),Rad51(c.-3429G> C)多态性之间的关联。 ,c.-3392G> T),Lig4(c.26C> T,c.1704T> C),Ku70(c.-1310C> G)和Ku80(c.2110-2408G> A)和急性发作放疗后的反应。材料与方法:研究人群包括88位经强度调制放射治疗(IMRT)治疗的头颈癌患者。黏膜炎,皮炎和吞咽困难使用不良事件v.3.0量表的通用术语标准(CTC)进行评分。将人群分为CTC0-2和CTC3 +组,以分析每种急性作用。使用剂量-体积直方图分析了剂量对关键结构的影响。通过聚合酶链反应(PCR)结合限制性片段长度多态性或PCR单碱基延伸分析来确定基因型。结果:口腔和咽喉(PC)肌肉的平均剂量(D(平均值))分别与粘膜炎和吞咽困难的发生显着相关。这些参数在放射基因组学分析中被认为是混杂因素。 XRCC3c.722CT / TT和Ku70c.-1310CG / GG基因型与严重吞咽困难(CTC3 +)的发生密切相关。在研究的多态性与粘膜炎或皮炎的发展之间未发现关联。基于XRCC3c.722CT / TT和Ku70c.-1310CG / GG基因型和PC剂量开发的严重吞咽困难风险分析模型显示敏感性为78.6%,特异性为77.6%。结论:XRCC3c.722C> T和Ku70c.-1310C> G多态性以及PC肌肉的D(均值)与IMRT后严重吞咽困难的发生高度相关。使用这些参数开发的预测模型显示出很高的灵敏度和特异性。

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