基于剂量-线性能量转移(LET)体积约束的点扫描质子治疗稳健优化。

IF 6.4 1区 医学 Q1 ONCOLOGY
Jingyuan Chen, Yunze Yang, Hongying Feng, Lian Zhang, Zhengliang Liu, Tianming Liu, Carlos E Vargas, Nathan Y Yu, Jean-Claude M Rwigema, Sameer R Keole, Samir H Patel, Sujay A Vora, Jiajian Shen, Wei Liu
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引用次数: 0

摘要

目的:一直以来,点扫描质子治疗(SSPT)的治疗规划分别利用剂量体积约束和线性能量转移(LET)体积约束来平衡肿瘤控制和危险器官(OARs)保护。我们为治疗前列腺癌的 SSPT 提出了一种基于剂量-线性能量传递体积约束(DLVC)的鲁棒性优化(DLVCRO)新方法,以获得理想的联合剂量和线性能量传递分布,从而最大限度地减少不良事件(AEs):方法:DLVCRO 将 DLVC 视为控制剂量-LET 容量直方图(DLVH)曲线形状的软约束。方法:DLVCRO 将 DLVC 作为软约束,控制剂量-LET 容量直方图(DLVH)曲线的形状,最大限度地减少 OAR 中高 LET 和高剂量的重叠,并以用户定义的方式将 OAR 中的高 LET 重新分配到靶点。这项回顾性研究共纳入了 10 名前列腺癌患者。直肠和膀胱被视为 OAR。DLVCRO 与传统的稳健优化(RO)方法进行了比较。使用最坏情况分析方法对计划的稳健性进行了量化。除了剂量-体积直方图(DVH)指数外,还使用了类似的 LET-体积直方图(LETVH)、生物外剂量(每个体素剂量与 LET 的乘积)-体积直方图(xBDVH)指数来描述联合剂量/LET 分布和 DLVH 指数。采用 Wilcoxon 符号秩检验来衡量统计显著性:结果:在名义情景下,与 RO 相比,DLVCRO 能显著改善剂量和 LET 的联合分布,从而保护 OAR。目标和 OAR 的物理剂量分布相当。在最坏情况下,DLVCRO 明显增强了对 OAR 的保护(更稳健),同时在目标剂量覆盖率和均匀性方面保持了几乎相同的计划稳健性:结论:DLVCRO将基于二维DVH的治疗计划升级为基于三维DLVH的治疗计划,可同时稳健地调整剂量/LET分布。DLVCRO 有可能成为改善 SSPT 患者预后的有力工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Robust Optimization for Spot-Scanning Proton Therapy based on Dose-Linear-Energy-Transfer Volume Constraints.

Purpose: Historically, spot-scanning proton therapy (SSPT) treatment planning uses dose-volume constraints and linear-energy-transfer (LET) volume constraints separately to balance tumor control and organs-at-risk (OARs) protection. We propose a novel dose-LET-volume constraint (DLVC)-based robust optimization (DLVCRO) method for SSPT in treating prostate cancer to obtain a desirable joint dose and LET distribution to minimize adverse events.

Methods and materials: DLVCRO treats DLVC as soft constraints that control the shapes of the dose-LET volume histogram (DLVH) curves. It minimizes the overlap of high LET and high dose in OARs and redistributes high LET from OARs to targets in a user-defined way. Ten patients with prostate cancer were included in this retrospective study. Rectum and bladder were considered as OARs. DLVCRO was compared with the conventional robust optimization (RO) method. Plan robustness was quantified using the worst-case analysis method. Besides the dose-volume histogram indices, the analogous LET-volume histogram, extrabiological dose (the product of per voxel dose and LET) volume histogram (xBDVH) indices characterizing the joint dose/LET distributions and DLVH indices were also used. The Wilcoxon signed-rank test was performed to measure statistical significance.

Results: In the nominal scenario, DLVCRO significantly improved joint distribution of dose and LET to protect OARs compared with RO. The physical dose distributions in targets and OARs are comparable. In the worst-case scenario, DLVCRO markedly enhanced OAR protection (more robust) while maintaining almost the same plan robustness in target dose coverage and homogeneity.

Conclusions: DLVCRO upgrades 2D DVH-based to 3D DLVH-based treatment planning to adjust dose/LET distributions simultaneously and robustly. DLVCRO is potentially a powerful tool to improve patient outcomes in SSPT.

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来源期刊
CiteScore
11.00
自引率
7.10%
发文量
2538
审稿时长
6.6 weeks
期刊介绍: International Journal of Radiation Oncology • Biology • Physics (IJROBP), known in the field as the Red Journal, publishes original laboratory and clinical investigations related to radiation oncology, radiation biology, medical physics, and both education and health policy as it relates to the field. This journal has a particular interest in original contributions of the following types: prospective clinical trials, outcomes research, and large database interrogation. In addition, it seeks reports of high-impact innovations in single or combined modality treatment, tumor sensitization, normal tissue protection (including both precision avoidance and pharmacologic means), brachytherapy, particle irradiation, and cancer imaging. Technical advances related to dosimetry and conformal radiation treatment planning are of interest, as are basic science studies investigating tumor physiology and the molecular biology underlying cancer and normal tissue radiation response.
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