Dosimetric analysis of brachial plexopathy after stereotactic body radiotherapy: Significance of organ delineation

医学 轮廓 核医学 臂丛神经病变 臂丛神经 放射治疗 线性回归 逻辑回归 放射科 外科 内科学 数学 工程制图 工程类 统计
作者
Geng-Min Niu,Miaomiao Gao,Xiaofeng Wang,Yang Dong,Qian Zhang,Huanhuan Wang,Yong Guan,Zhiyong Yuan,Shu-Zhou Zhao,Yongchun Song,Zhen Tao,Lujun Zhao,Maobin Meng,Feng‐Ming Kong,Zhiyong Yuan
出处
期刊:Radiotherapy and Oncology [Elsevier]
卷期号:190: 110023-110023 被引量:1
标识
DOI:10.1016/j.radonc.2023.110023
摘要

Objectives Examine the significance of contouring the brachial plexus (BP) for toxicity estimation and select metrics for predicting radiation-induced brachial plexopathy (RIBP) after stereotactic body radiotherapy. Materials and Methods Patients with planning target volume (PTV) ≤ 2 cm from the BP were eligible. The BP was contoured primarily according to the RTOG 1106 atlas, while subclavian-axillary veins (SAV) were contoured according to RTOG 0236. Apical PTVs were classified as anterior (PTV-A) or posterior (PTV-B) PTVs. Variables predicting grade 2 or higher RIBP (RIBP2) were selected through least absolute shrinkage and selection operator regression and logistic regression. Results Among 137 patients with 140 BPs (median follow-up, 32.1 months), 11 experienced RIBP2. For patients with RIBP2, the maximum physical dose to the BP (BP-Dmax) was 46.5 Gy (median; range, 35.7 to 60.7 Gy). Of these patients, 54.5 % (6/11) satisfied the RTOG limits when using SAV delineation; among them, 83.3 % (5/6) had PTV-B. For patients with PTV-B, the maximum physical dose to SAV (SAV-Dmax) was 11.2 Gy (median) lower than BP-Dmax. Maximum and 0.3 cc biologically effective doses to the BP based on the linear-quadratic-linear model (BP-BEDmax LQL and BP-BED0.3cc LQL, α/β = 3) were selected as predictive variables with thresholds of 118 and 73 Gy, respectively. Conclusion Contouring SAV may significantly underestimate the RIBP2 risk in dosimetry, especially for patients with PTV-B. BP contouring indicated BP-BED0.3cc LQL and BP-BEDmax LQL as potential predictors of RIBP2.
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