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Radiation-induced late dysphagia after intensity-modulated radiotherapy in nasopharyngeal carcinoma patients: a dose-volume effect analysis

机译:鼻咽癌患者调强放疗后放射诱发的晚期吞咽困难:剂量-体积效应分析

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摘要

Dysphagia is a side effect of nasopharyngeal carcinoma chemo-radiotherapy (CRT) which greatly influences the quality of life of the patients. We analyzed late dysphagia in 134 patients with nasopharyngeal cancer undergoing radical radiotherapy (RT), and correlated these findings with dose–volume histogram (DVH) parameters of the swallowing organs at risk (SWOARs). DVH parameters of SWOARs were correlated with late dysphagia, and with RTOG/EORTC scale score and the M. D. Anderson dysphagia inventory (MDADI) score. The mean dose (Dmean) to the superior and inferior constrictor muscles (SCM and ICM) and age were associated with grade 2 late dysphagia. Receiver operating characteristic (ROC) curves showed that the threshold values for grade 2 late dysphagia were: Dmean to SCM ≥ 67 Gy, partial volume receiving specified dose of 60 Gy (V60) of SCM ≥ 95%, Dmean to ICM ≥ 47 Gy, and V50 of ICM ≥ 23%. The areas under the ROC curve were 0.681 (p = 0.02), 0.677 (p = 0.002), 0.71 (p < 0.001) and 0.726 (p < 0.001) respectively. Our study demonstrates a significant relationship between late dysphagia and the radiation doses delivered to the SCM and ICM. Our findings suggest that physicians should be cautious in reducing the RT dose to SWOARs in order to avoid severe dysphagia. Further prospective trials are necessary to recommend this as part of routine clinical practice.
机译:吞咽困难是鼻咽癌化学放射疗法(CRT)的副作用,它极大地影响了患者的生活质量。我们分析了接受根治性放疗(RT)的134例鼻咽癌患者的晚期吞咽困难,并将这些发现与吞咽危险器官(SWOARs)的剂量-体积直方图(DVH)参数相关。 SWOAR的DVH参数与晚期吞咽困难,RTOG / EORTC量表评分和M.D. Anderson吞咽困难量表(MDADI)评分相关。上,下收缩肌(SCM和ICM)的平均剂量(Dmean)和年龄与2级晚期吞咽困难有关。接收器工作特征(ROC)曲线显示,2级晚期吞咽困难的阈值为:Dmean至SCM≥67 Gy,部分体积接受指定剂量的60 Gy(V60)SCM≥95%,Dmean至ICM≥47 Gy, ICM的V50≥23%。 ROC曲线下的面积分别为0.681(p = 0.02),0.677(p = 0.002),0.71(p <0.001)和0.726(p <0.001)。我们的研究表明,晚期吞咽困难与输送至SCM和ICM的辐射剂量之间存在显着关系。我们的发现表明,医师应谨慎减少SWOAR的RT剂量,以避免严重吞咽困难。有必要进行进一步的前瞻性试验,以将其推荐为常规临床实践的一部分。

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