MSOR2 Presentation Time: 5:05 PM

IF 1.7 4区 医学 Q4 ONCOLOGY Brachytherapy Pub Date : 2024-10-25 DOI:10.1016/j.brachy.2024.08.036
Mahdokht Akbari Taemeh PhD Candidate , Théophraste Lescot M.Sc. , Marc-André Fortin Ing., Ph.D.
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In this study, a homogeneous PGD formulation based on methacrylic acid (MAA, the reactive monomer) was optimized to meet these challenges. A dosimetry assessment methodology was elaborated for LDR-BT devices, involving the measurement of gel response to LEP using MRI (3 magnetic fields: 1, 1.5, 3T) and experimental dose profiles were generated in PGDs upon exposure to 3D-printed plaques containing <sup>125</sup>I seeds and numerically plotted in 3D.</div></div><div><h3>Materials and Methods</h3><div><em>Single Seed Experiment (SSE):</em> a MAGIC-f gel formulation<sup>3</sup> was optimized by adding 0.75 %w/w paraformaldehyde (PF) as gelatin crosslinker. Gelatin and PF were dissolved in pure water and mixed at 45°C. CopperII sulfate pentahydrate, L-ascorbic acid and MAA were added at 37°C. The solution was gelified in a glass container at 4°C overnight. Formed gels were exposed to a <sup>125</sup>I seed (OncoSeed 6711, activity: 2.13 mCi; n=3) placed in a fixed glass tube for 54h at RT (Fig1a). The gels were MRI-scanned (<em>T<sub>2</sub></em>-w) with 0.9 × 0.9 × 0.9 mm<sup>3</sup> voxel size using 1T, 1.5T and 3T MRI (TR/TE= 3585(1T)-4350(1.5T)-5410(3T)/22-352ms). <em>T<sub>2</sub></em> (=1/ <em>R<sub>2</sub></em>) maps were generated across the vial axial plane. The TOPAS Monte Carlo (MC) code toolkit was used to calculate the absolute dose deposited in the gel with a similar seed model and the <em>R<sub>2</sub></em>-dose calibration curve was plotted. Gel water equivalency was assessed by MC, comparing the percentage depth dose (PDD) delivered to water and gel phantoms when exposed to <sup>125</sup>I seeds. Gel thermal and temporal stability were assessed up to 70 °C and over 7 days, respectively. <em>Dose profile visualization:</em> A two-part box and a plaque with 3 holes (1 × 1.5 mm diam/depth) were 3D-printed (Apium P220 printer) in PEEK as the gel container and <sup>125</sup>I seed holder, respectively (Fig1e). The gel was prepared (SSE protocol) and exposed to the plaque for 54h (avg. activity: 1.58 mCi; n=3) followed by 3T <em>T<sub>2</sub></em>-w MRI scanning. The dose was visualized in 3D using the calibration curve and the Python code using Plotly Library.</div></div><div><h3>Results</h3><div>The results showed that MAGIC-f gel is water equivalent (gel/water PDD ∼1), thermally (up to 70 °C) and temporally stable for 7 days at RT. The SEE results showed detection range of 10-20, 7-25 and 8-22 Gy and sensitivity of 0.6, 0.35 and 0.44 Gy<sup>-1</sup>s<sup>-1</sup> for 1T, 1.5T, 3T MRI scans, respectively (Fig1d); that are at least 3 times more sensitivity to LEP than for the only equivalent study reported in the literature<sup>2b</sup>. While 1T MRI scanning gives the highest gel sensitivity, lower dose values and broader dose range could be detected with 1.5 and 3T MRI. Fig1i indicates the 3D dose distribution delivered by the 3D-printed LDR plaque validating the gel functionality to visualize the dose profile with high resolution in 3D.</div></div><div><h3>Conclusions</h3><div>A MAGIC-f gel formulation optimized for LDR-BT applications is thermally and temporally stable and water equivalent. It can detect small dose changes induced by LEP, with high sensitivity and resolution. This gel is a promising tool for developing the clinical workflow including dose profile assessments, required for 3D-printed personalized LDR-BT devices.[1] Lescot et al Adv Health Mater 12.25 2023 [2] Pantelis et al Phys Med Biol (a) 49.15 2004 &amp; (b) 50.18 2005 [3] Fernandes et al JPCS 164.1 2009</div></div>","PeriodicalId":55334,"journal":{"name":"Brachytherapy","volume":null,"pages":null},"PeriodicalIF":1.7000,"publicationDate":"2024-10-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Brachytherapy","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1538472124001727","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"ONCOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Purpose

Personalized 3D-printed brachytherapy (BT) implants and advanced dose painting methods for better-targeting tumor geometry, could improve BT outcomes1. One challenge in this approach is the necessity of measuring the dose profile for each device, before implantation. Polymer gel dosimeters (PGD) could meet the dosimetry challenges of personalized BT devices. However, PGDs have been mainly used in external beam therapy applications and at high-energy photons; by comparison for low-dose-rate (LDR) BT, low-energy photons (LEP) raise issues of water equivalency, energy response2a and longer exposure times. In this study, a homogeneous PGD formulation based on methacrylic acid (MAA, the reactive monomer) was optimized to meet these challenges. A dosimetry assessment methodology was elaborated for LDR-BT devices, involving the measurement of gel response to LEP using MRI (3 magnetic fields: 1, 1.5, 3T) and experimental dose profiles were generated in PGDs upon exposure to 3D-printed plaques containing 125I seeds and numerically plotted in 3D.

Materials and Methods

Single Seed Experiment (SSE): a MAGIC-f gel formulation3 was optimized by adding 0.75 %w/w paraformaldehyde (PF) as gelatin crosslinker. Gelatin and PF were dissolved in pure water and mixed at 45°C. CopperII sulfate pentahydrate, L-ascorbic acid and MAA were added at 37°C. The solution was gelified in a glass container at 4°C overnight. Formed gels were exposed to a 125I seed (OncoSeed 6711, activity: 2.13 mCi; n=3) placed in a fixed glass tube for 54h at RT (Fig1a). The gels were MRI-scanned (T2-w) with 0.9 × 0.9 × 0.9 mm3 voxel size using 1T, 1.5T and 3T MRI (TR/TE= 3585(1T)-4350(1.5T)-5410(3T)/22-352ms). T2 (=1/ R2) maps were generated across the vial axial plane. The TOPAS Monte Carlo (MC) code toolkit was used to calculate the absolute dose deposited in the gel with a similar seed model and the R2-dose calibration curve was plotted. Gel water equivalency was assessed by MC, comparing the percentage depth dose (PDD) delivered to water and gel phantoms when exposed to 125I seeds. Gel thermal and temporal stability were assessed up to 70 °C and over 7 days, respectively. Dose profile visualization: A two-part box and a plaque with 3 holes (1 × 1.5 mm diam/depth) were 3D-printed (Apium P220 printer) in PEEK as the gel container and 125I seed holder, respectively (Fig1e). The gel was prepared (SSE protocol) and exposed to the plaque for 54h (avg. activity: 1.58 mCi; n=3) followed by 3T T2-w MRI scanning. The dose was visualized in 3D using the calibration curve and the Python code using Plotly Library.

Results

The results showed that MAGIC-f gel is water equivalent (gel/water PDD ∼1), thermally (up to 70 °C) and temporally stable for 7 days at RT. The SEE results showed detection range of 10-20, 7-25 and 8-22 Gy and sensitivity of 0.6, 0.35 and 0.44 Gy-1s-1 for 1T, 1.5T, 3T MRI scans, respectively (Fig1d); that are at least 3 times more sensitivity to LEP than for the only equivalent study reported in the literature2b. While 1T MRI scanning gives the highest gel sensitivity, lower dose values and broader dose range could be detected with 1.5 and 3T MRI. Fig1i indicates the 3D dose distribution delivered by the 3D-printed LDR plaque validating the gel functionality to visualize the dose profile with high resolution in 3D.

Conclusions

A MAGIC-f gel formulation optimized for LDR-BT applications is thermally and temporally stable and water equivalent. It can detect small dose changes induced by LEP, with high sensitivity and resolution. This gel is a promising tool for developing the clinical workflow including dose profile assessments, required for 3D-printed personalized LDR-BT devices.[1] Lescot et al Adv Health Mater 12.25 2023 [2] Pantelis et al Phys Med Biol (a) 49.15 2004 & (b) 50.18 2005 [3] Fernandes et al JPCS 164.1 2009
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MSOR2 演讲时间:下午 5:05
目的个性化三维打印近距离放射治疗(BT)植入物和先进的剂量绘制方法可更好地瞄准肿瘤几何形状,从而改善近距离放射治疗的效果1。这种方法面临的一个挑战是必须在植入前测量每个装置的剂量曲线。聚合物凝胶剂量计(PGD)可以应对个性化 BT 设备的剂量测定挑战。然而,PGD 主要用于体外射束治疗和高能光子;相比之下,对于低剂量率(LDR)BT,低能光子(LEP)会引起水当量、能量响应2a 和更长照射时间等问题。本研究优化了基于甲基丙烯酸(MAA,活性单体)的均质 PGD 配方,以应对这些挑战。针对 LDR-BT 设备制定了剂量测定评估方法,包括使用 MRI(3 个磁场:1、1.5、3T)测量凝胶对 LEP 的响应,以及在 PGD 中生成暴露于含有 125I 种子的 3D 打印斑块时的实验剂量曲线,并以 3D 形式绘制数值曲线。明胶和多聚甲醛溶于纯水,在 45°C 下混合。在 37°C 时加入五水硫酸铜、L-抗坏血酸和 MAA。溶液在 4°C 的玻璃容器中凝胶化过夜。将形成的凝胶置于固定玻璃管中的 125I 种子(OncoSeed 6711,活性:2.13 mCi;n=3)中,在 RT 下暴露 54 小时(图 1a)。使用 1T、1.5T 和 3T 核磁共振成像(TR/TE= 3585(1T)-4350(1.5T)-5410(3T)/22-352ms)对凝胶进行 0.9 × 0.9 × 0.9 mm3 体素扫描(T2-w)。T2(=1/ R2)图是在整个小瓶轴向平面生成的。使用 TOPAS Monte Carlo(MC)代码工具包计算类似种子模型沉积在凝胶中的绝对剂量,并绘制 R2 剂量校准曲线。通过 MC 评估凝胶水当量,比较暴露于 125I 种子时水和凝胶模型的深度剂量百分比 (PDD)。凝胶的热稳定性和时间稳定性分别在 70 °C 和 7 天内进行了评估。剂量曲线可视化:用聚醚醚酮(PEEK)材料 3D 打印了一个两部分组成的盒子和一个带 3 个孔(直径/深度为 1 × 1.5 毫米)的斑块,分别作为凝胶容器和 125I 种子支架(图 1e)。制备凝胶(SSE 方案)并在斑块上暴露 54 小时(平均活性:1.58 mCi;n=3),然后进行 3T T2-w MRI 扫描。结果表明,MAGIC-f 凝胶具有水当量(凝胶/水 PDD ∼1)、热稳定性(高达 70 °C)以及在 RT 条件下 7 天的时间稳定性。SEE 结果显示,1T、1.5T 和 3T MRI 扫描的检测范围分别为 10-20、7-25 和 8-22Gy,灵敏度分别为 0.6、0.35 和 0.44Gy-1s-1(图 1d);与文献2b 报道的唯一等效研究相比,LEP 灵敏度至少提高了 3 倍。虽然 1T 磁共振成像扫描的凝胶灵敏度最高,但 1.5T 和 3T 磁共振成像可检测到更低的剂量值和更宽的剂量范围。图 1i 显示了三维打印 LDR 斑块的三维剂量分布,验证了凝胶在三维高分辨率下可视化剂量曲线的功能。它能以高灵敏度和高分辨率检测 LEP 引起的微小剂量变化。[1]Lescot et al Adv Health Mater 12.25 2023 [2] Pantelis et al Phys Med Biol (a) 49.15 2004 & (b) 50.18 2005 [3] Fernandes et al JPCS 164.1 2009
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来源期刊
Brachytherapy
Brachytherapy 医学-核医学
CiteScore
3.40
自引率
21.10%
发文量
119
审稿时长
9.1 weeks
期刊介绍: Brachytherapy is an international and multidisciplinary journal that publishes original peer-reviewed articles and selected reviews on the techniques and clinical applications of interstitial and intracavitary radiation in the management of cancers. Laboratory and experimental research relevant to clinical practice is also included. Related disciplines include medical physics, medical oncology, and radiation oncology and radiology. Brachytherapy publishes technical advances, original articles, reviews, and point/counterpoint on controversial issues. Original articles that address any aspect of brachytherapy are invited. Letters to the Editor-in-Chief are encouraged.
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Editorial Board Masthead Table of Contents Thursday, July 11, 20244:00 PM - 5:00 PM PP01 Presentation Time: 4:00 PM MSOR12 Presentation Time: 5:55 PM
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