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为临床使用委托和基准测试三维剂量测定系统。

Commissioning and benchmarking a 3D dosimetry system for clinical use.

机构信息

Duke University Medical Center, Durham, North Carolina 27710, USA.

出版信息

Med Phys. 2011 Aug;38(8):4846-57. doi: 10.1118/1.3611042.

Abstract

PURPOSE

A 3D dosimetry system is described which consists of two parts: a radiochromic plastic dosimeter PRESAGE (which responds to absorbed dose with a linear change in optical-density) and the Duke large-field-of-view optical-CT scanner (DLOS). The DLOS/PRESAGE system has recently been commissioned and benchmarked for clinical use and, in particular, for verification and commissioning of complex radiation treatments.

METHODS

DLOS commissioning involved determining the dynamic range, spatial resolution, noise, temporal, and other characteristics of the light source and imaging components. Benchmarking tests were performed on the combined DLOS/PRESAGE system to establish baseline dosimetric performance. The tests consisted of delivering simple radiation treatments to PRESAGE dosimeters, and comparing the measured 3D relative dose distributions with the known gold standard. The gold standard distribution was obtained from machine beam-data or the treatment planning system (TPS). All studies used standardized procedures to ensure consistency.

RESULTS

For commissioning, isotropic spatial resolution was submillimeter (MTF > 0.5 for frequencies of 1.5 lp/mm) and the dynamic range was -60 dB. Flood field uniformity was within 10% and stable after 45 min of warm-up. Stray-light is small, due to telecentricity, but even the residual can be removed through deconvolution by a point-spread-function. For benchmarking, the mean 3D passing NDD (normalized dose distribution) rate (3%, 3mm, 5% dose threshold) over the benchmark data sets was 97.3% +/- 0.6% (range 96%-98%), which is on par with other planar dosimeters used in external beam radiation therapy indicating excellent agreement. Noise was low at < 2% of maximum dose (4-12 Gy) for 2 mm reconstructions. The telecentric design was critical to enabling fast imaging with minimal stray-light artifacts.

CONCLUSIONS

This work presents the first comprehensive benchmarking of a 3D dosimetry system for clinical use. The DLOS/PRESAGE benchmark tests show consistently good agreement to simple known distributions. The system produces accurate isotropic 2 mm dose data over clinical volumes (e.g., 16 cm diameter phantoms, 12 cm height), in under 15 min. It represents a uniquely useful and versatile new tool for commissioning and verification of complex therapy treatments.

摘要

目的

本文描述了一种由两部分组成的 3D 剂量测定系统:光致变色塑料剂量计 PRESAGE(其光学密度随吸收剂量线性变化)和杜克大视场光学 CT 扫描仪(DLOS)。DLOS/PRESAGE 系统最近已获得临床使用的许可和基准测试,特别是用于验证和调试复杂的放射治疗。

方法

DLOS 的调试包括确定光源和成像组件的动态范围、空间分辨率、噪声、时间等特性。对组合的 DLOS/PRESAGE 系统进行了基准测试,以建立基本的剂量测定性能。测试包括将简单的放射治疗应用于 PRESAGE 剂量计,并将测量的 3D 相对剂量分布与已知的金标准进行比较。金标准分布是从机器束数据或治疗计划系统(TPS)获得的。所有研究都使用标准化程序以确保一致性。

结果

对于调试,各向同性空间分辨率为亚毫米级(对于 1.5 lp/mm 的频率,MTF > 0.5),动态范围为-60dB。漫射场均匀性在预热 45 分钟后保持在 10%以内且稳定。由于远心度,杂散光很小,但即使是残余杂散光也可以通过点扩散函数的反卷积去除。对于基准测试,基准数据集的平均 3D 通过 NDD(归一化剂量分布)率(3%、3mm、5%剂量阈值)为 97.3% +/- 0.6%(范围为 96%-98%),与用于外束放射治疗的其他平面剂量计相当,表明一致性很好。对于 2mm 重建,噪声低于最大剂量的 2%(4-12Gy)。远心设计对于实现快速成像和最小化杂散光伪影至关重要。

结论

本文首次全面基准测试了一种用于临床使用的 3D 剂量测定系统。DLOS/PRESAGE 基准测试始终与简单的已知分布很好地一致。该系统在不到 15 分钟的时间内即可在临床体积(例如,直径 16cm 的体模,高 12cm)内生成准确的各向同性 2mm 剂量数据。它代表了一种独特的有用且多功能的新工具,可用于复杂治疗方案的调试和验证。

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