Effects of axillary dose restriction on plan quality and acute radiation dermatitis in breast cancer radiotherapy.

IF 1.1 4区 医学 Q4 ONCOLOGY
Meizhen Shen, Meizhu Shen, Ying Mo, Chunming Lin, Jian Qin
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引用次数: 0

Abstract

Axillary dose restriction (ADR) is rarely implemented in breast cancer radiotherapy by radiation oncologists to minimize exposure to organs at risk (OARs), particularly the axilla. This prospective randomized controlled study aims to evaluate the efficacy of ADR in improving plan quality (PQ) and its impact on acute radiation dermatitis (ARD) in breast cancer radiotherapy. The study recruited breast cancer patients who required postoperative radiotherapy but did not have an indication for axillary irradiation. Delineation and dosimetric assessment of the axilla (Axilla Levels I-III and Axillary Cavity) were performed in all cases, with ADR implemented randomly. ADR involved restricting the mean axilla dose to 40-45 Gy during radiotherapy. The outcomes assessed included the ARD grades (both overall and axillary) and dose-volume parameters of PQ including skin V35. The study enrolled 87 patients, who were randomly divided into two groups: Group I (50 patients) received ADR, while Group C (37 patients) did not. ADR was found to be significantly associated with reduced exposure doses to the axilla and ipsilateral lung, specifically in patients with modified radical mastectomy (MRM). Results of other PQ parameters, such as D95, V93, V95, V100, V107 for the planning target volume (PTV), V30, Dmean for the heart, Dmax for the spinal cord, and V5 for the ipsilateral lung, demonstrated potential benefits in alleviating doses to these OARs while maintaining optimized PQ, although these results were not statistically significant. However, no statistically significant correlation between ADR and severe ARD (≥ Grade 2) or skin V35 was established, either in the total patient population or in subgroups. Additionally, a multivariable logistic regression for severe ARD was conducted, with ADR and skin V35 included as predictive factors. Only older age was found to be significantly associated with severe ARD. Implementing ADR in breast cancer radiotherapy not only protects the axilla and ipsilateral lung but also maintains optimized PQ, specifically in MRM patients, though it shows no evidence of alleviating ARD. Adopting ADR may be considered a valuable option in breast cancer radiotherapy.

腋窝剂量限制对乳腺癌放疗计划质量及急性放射性皮炎的影响。
腋窝剂量限制(ADR)在乳腺癌放疗中很少由放射肿瘤学家实施,以尽量减少暴露于危险器官(OARs),特别是腋窝。本前瞻性随机对照研究旨在评价乳腺癌放疗中不良反应对改善计划质量(PQ)的效果及其对急性放射性皮炎(ARD)的影响。该研究招募了需要术后放疗但没有腋窝放疗指征的乳腺癌患者。所有病例均进行腋窝(腋窝I-III级和腋窝腔)的划定和剂量学评估,随机进行不良反应。不良反应包括在放疗期间将平均腋窝剂量限制在40-45 Gy。评估的结果包括ARD分级(总体和腋窝)和PQ的剂量-体积参数(包括皮肤V35)。研究共纳入87例患者,随机分为两组:I组(50例)出现不良反应,C组(37例)未出现不良反应。发现不良反应与腋窝和同侧肺暴露剂量减少显著相关,特别是在改良乳房根治术(MRM)患者中。其他PQ参数的结果,如计划靶体积(PTV)的D95、V93、V95、V100、V107,心脏的V30、Dmean,脊髓的Dmax和同侧肺的V5,显示了在保持优化PQ的同时减轻这些OARs剂量的潜在益处,尽管这些结果没有统计学意义。然而,无论是在总患者群体中还是在亚组中,ADR与严重ARD(≥2级)或皮肤V35之间均无统计学意义的相关性。此外,对重度ARD进行多变量logistic回归,将ADR和皮肤V35作为预测因素。研究发现,只有年龄较大与严重ARD显著相关。在乳腺癌放疗中实施ADR不仅可以保护腋窝和同侧肺,还可以维持最佳的PQ,特别是在MRM患者中,尽管没有证据表明它可以缓解ARD。采用不良反应可能被认为是乳腺癌放疗的一个有价值的选择。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Medical Dosimetry
Medical Dosimetry 医学-核医学
CiteScore
2.40
自引率
0.00%
发文量
51
审稿时长
34 days
期刊介绍: Medical Dosimetry, the official journal of the American Association of Medical Dosimetrists, is the key source of information on new developments for the medical dosimetrist. Practical and comprehensive in coverage, the journal features original contributions and review articles by medical dosimetrists, oncologists, physicists, and radiation therapy technologists on clinical applications and techniques of external beam, interstitial, intracavitary and intraluminal irradiation in cancer management. Articles dealing primarily with physics will be reviewed by a specially appointed team of experts in the field.
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