PO37

Michael Salerno, Rachel Trevillian, Shibu Anamalayil, Megan Kassick, Seung Won Seol, Neil Taunk, Emily Hubley
{"title":"PO37","authors":"Michael Salerno, Rachel Trevillian, Shibu Anamalayil, Megan Kassick, Seung Won Seol, Neil Taunk, Emily Hubley","doi":"10.1016/j.brachy.2023.06.138","DOIUrl":null,"url":null,"abstract":"Purpose Treating multiple fractions of cervical HDR BT with a single implant can reduce the overall package time of the procedure and reduces patient anesthesia and radiation oncology personnel resources due to reduced numbers of plans generated. Intracavitary (IC) and Intracavitary/Interstitial (IC/IS) applicators can shift between brachytherapy fractions, and bladder and bowel filling can cause interfraction variations of OAR dosimetry. Interfraction dosimetry variations of single implants have not been well-quantified and it is unclear whether an adaptive replan is required for each fraction. Methods and Materials 10 patients with locally advanced cervical cancer treated with HDR BT were included in this study: 5 consecutive IC (T&R applicator) and 5 consecutive hybrid IC/IS (T&R with interstitial needles). Each patient received 45Gy in 25 fractions of EBRT followed by 28Gy in 4 fractions of HDR MR-IGABT with Alatus Vaginal Balloon packing (Radiadyne, Latham, NY). BT was administered using a two-implant technique. After the first implant, fraction 1 was planned and delivered using CT and MRI. After overnight admission, a new CT was obtained prior to fraction 2 and rigidly registered to the fraction 1 CT using the applicator and cervix as landmarks. The bladder, rectum, and sigmoid colon were contoured and the treatment plan for fraction 1 was copied onto the fraction 2 CT. The same procedure was applied for fractions 3 and 4 with a new implant followed by a CT/MR-based plan generated for fraction 3, and an evaluation CT for fraction 4. The absolute interfraction change in EQD2 and cumulative EBRT+BT was calculated using an alpha/beta value of 3; all doses are reported in EQD2. Differences in interfraction variability between IC and IC/IS plans were investigated. Results The mean HRCTV volume was 17.8cc (8.1-27cc) for IC plans and 32.6cc (19.6-44.4cc) for IC/IS plans. All IC/IS plans had an average fraction of total dwell time of less than 20% in needles. The D2cc for bladder, rectum, and sigmoid were below the soft/hard EMBRACE II guidelines for all plans (80/90Gy, 65/75Gy, 65/75Gy, respectively). The mean single BT fraction D2cc to bladder, rectum, and sigmoid were 7.9Gy, 2.9Gy and 4.2Gy. The bladder D2cc displayed the greatest interfraction variability, with an average absolute interfraction difference of 1.8±1.3Gy, while rectum and sigmoid were 0.6±0.5Gy and 0.7±0.7Gy. Differences between IC and IC/IS plans were also compared. The mean single fraction D2cc to bladder was lower for IC/IS plans (7.2±1.0Gy) as compared to IC plans (8.7±0.4Gy). The mean single fraction D2cc to rectum and sigmoid were similar between the two methods (2.8±0.3Gy and 4.3±0.3Gy for IC/IS versus 2.9±0.3Gy and 4.1±0.3Gy for IC). The absolute interfraction D2cc difference was minimal with both applicators (Figure 1). The interfraction D2cc difference to bladder, rectum, and sigmoid was similar for IC/IS plans (1.8±1.1Gy, 0.6±0.5Gy and 0.7±0.8Gy) as compared to IC plans (1.8±1.4Gy, 0.5±0.4, 0.6±0.7Gy). Conclusion Overall, the dose to the organs at risk was within the acceptable limits for all fraction plans. The dose differences between the two applicators were minimal, demonstrating that an overnight treatment procedure using IC and IC/IS plans is a viable option. Treating multiple fractions of cervical HDR BT with a single implant can reduce the overall package time of the procedure and reduces patient anesthesia and radiation oncology personnel resources due to reduced numbers of plans generated. Intracavitary (IC) and Intracavitary/Interstitial (IC/IS) applicators can shift between brachytherapy fractions, and bladder and bowel filling can cause interfraction variations of OAR dosimetry. Interfraction dosimetry variations of single implants have not been well-quantified and it is unclear whether an adaptive replan is required for each fraction. 10 patients with locally advanced cervical cancer treated with HDR BT were included in this study: 5 consecutive IC (T&R applicator) and 5 consecutive hybrid IC/IS (T&R with interstitial needles). Each patient received 45Gy in 25 fractions of EBRT followed by 28Gy in 4 fractions of HDR MR-IGABT with Alatus Vaginal Balloon packing (Radiadyne, Latham, NY). BT was administered using a two-implant technique. After the first implant, fraction 1 was planned and delivered using CT and MRI. After overnight admission, a new CT was obtained prior to fraction 2 and rigidly registered to the fraction 1 CT using the applicator and cervix as landmarks. The bladder, rectum, and sigmoid colon were contoured and the treatment plan for fraction 1 was copied onto the fraction 2 CT. The same procedure was applied for fractions 3 and 4 with a new implant followed by a CT/MR-based plan generated for fraction 3, and an evaluation CT for fraction 4. The absolute interfraction change in EQD2 and cumulative EBRT+BT was calculated using an alpha/beta value of 3; all doses are reported in EQD2. Differences in interfraction variability between IC and IC/IS plans were investigated. The mean HRCTV volume was 17.8cc (8.1-27cc) for IC plans and 32.6cc (19.6-44.4cc) for IC/IS plans. All IC/IS plans had an average fraction of total dwell time of less than 20% in needles. The D2cc for bladder, rectum, and sigmoid were below the soft/hard EMBRACE II guidelines for all plans (80/90Gy, 65/75Gy, 65/75Gy, respectively). The mean single BT fraction D2cc to bladder, rectum, and sigmoid were 7.9Gy, 2.9Gy and 4.2Gy. The bladder D2cc displayed the greatest interfraction variability, with an average absolute interfraction difference of 1.8±1.3Gy, while rectum and sigmoid were 0.6±0.5Gy and 0.7±0.7Gy. Differences between IC and IC/IS plans were also compared. The mean single fraction D2cc to bladder was lower for IC/IS plans (7.2±1.0Gy) as compared to IC plans (8.7±0.4Gy). The mean single fraction D2cc to rectum and sigmoid were similar between the two methods (2.8±0.3Gy and 4.3±0.3Gy for IC/IS versus 2.9±0.3Gy and 4.1±0.3Gy for IC). The absolute interfraction D2cc difference was minimal with both applicators (Figure 1). The interfraction D2cc difference to bladder, rectum, and sigmoid was similar for IC/IS plans (1.8±1.1Gy, 0.6±0.5Gy and 0.7±0.8Gy) as compared to IC plans (1.8±1.4Gy, 0.5±0.4, 0.6±0.7Gy). Overall, the dose to the organs at risk was within the acceptable limits for all fraction plans. The dose differences between the two applicators were minimal, demonstrating that an overnight treatment procedure using IC and IC/IS plans is a viable option.","PeriodicalId":93914,"journal":{"name":"Brachytherapy","volume":"23 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2023-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Brachytherapy","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1016/j.brachy.2023.06.138","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Purpose Treating multiple fractions of cervical HDR BT with a single implant can reduce the overall package time of the procedure and reduces patient anesthesia and radiation oncology personnel resources due to reduced numbers of plans generated. Intracavitary (IC) and Intracavitary/Interstitial (IC/IS) applicators can shift between brachytherapy fractions, and bladder and bowel filling can cause interfraction variations of OAR dosimetry. Interfraction dosimetry variations of single implants have not been well-quantified and it is unclear whether an adaptive replan is required for each fraction. Methods and Materials 10 patients with locally advanced cervical cancer treated with HDR BT were included in this study: 5 consecutive IC (T&R applicator) and 5 consecutive hybrid IC/IS (T&R with interstitial needles). Each patient received 45Gy in 25 fractions of EBRT followed by 28Gy in 4 fractions of HDR MR-IGABT with Alatus Vaginal Balloon packing (Radiadyne, Latham, NY). BT was administered using a two-implant technique. After the first implant, fraction 1 was planned and delivered using CT and MRI. After overnight admission, a new CT was obtained prior to fraction 2 and rigidly registered to the fraction 1 CT using the applicator and cervix as landmarks. The bladder, rectum, and sigmoid colon were contoured and the treatment plan for fraction 1 was copied onto the fraction 2 CT. The same procedure was applied for fractions 3 and 4 with a new implant followed by a CT/MR-based plan generated for fraction 3, and an evaluation CT for fraction 4. The absolute interfraction change in EQD2 and cumulative EBRT+BT was calculated using an alpha/beta value of 3; all doses are reported in EQD2. Differences in interfraction variability between IC and IC/IS plans were investigated. Results The mean HRCTV volume was 17.8cc (8.1-27cc) for IC plans and 32.6cc (19.6-44.4cc) for IC/IS plans. All IC/IS plans had an average fraction of total dwell time of less than 20% in needles. The D2cc for bladder, rectum, and sigmoid were below the soft/hard EMBRACE II guidelines for all plans (80/90Gy, 65/75Gy, 65/75Gy, respectively). The mean single BT fraction D2cc to bladder, rectum, and sigmoid were 7.9Gy, 2.9Gy and 4.2Gy. The bladder D2cc displayed the greatest interfraction variability, with an average absolute interfraction difference of 1.8±1.3Gy, while rectum and sigmoid were 0.6±0.5Gy and 0.7±0.7Gy. Differences between IC and IC/IS plans were also compared. The mean single fraction D2cc to bladder was lower for IC/IS plans (7.2±1.0Gy) as compared to IC plans (8.7±0.4Gy). The mean single fraction D2cc to rectum and sigmoid were similar between the two methods (2.8±0.3Gy and 4.3±0.3Gy for IC/IS versus 2.9±0.3Gy and 4.1±0.3Gy for IC). The absolute interfraction D2cc difference was minimal with both applicators (Figure 1). The interfraction D2cc difference to bladder, rectum, and sigmoid was similar for IC/IS plans (1.8±1.1Gy, 0.6±0.5Gy and 0.7±0.8Gy) as compared to IC plans (1.8±1.4Gy, 0.5±0.4, 0.6±0.7Gy). Conclusion Overall, the dose to the organs at risk was within the acceptable limits for all fraction plans. The dose differences between the two applicators were minimal, demonstrating that an overnight treatment procedure using IC and IC/IS plans is a viable option. Treating multiple fractions of cervical HDR BT with a single implant can reduce the overall package time of the procedure and reduces patient anesthesia and radiation oncology personnel resources due to reduced numbers of plans generated. Intracavitary (IC) and Intracavitary/Interstitial (IC/IS) applicators can shift between brachytherapy fractions, and bladder and bowel filling can cause interfraction variations of OAR dosimetry. Interfraction dosimetry variations of single implants have not been well-quantified and it is unclear whether an adaptive replan is required for each fraction. 10 patients with locally advanced cervical cancer treated with HDR BT were included in this study: 5 consecutive IC (T&R applicator) and 5 consecutive hybrid IC/IS (T&R with interstitial needles). Each patient received 45Gy in 25 fractions of EBRT followed by 28Gy in 4 fractions of HDR MR-IGABT with Alatus Vaginal Balloon packing (Radiadyne, Latham, NY). BT was administered using a two-implant technique. After the first implant, fraction 1 was planned and delivered using CT and MRI. After overnight admission, a new CT was obtained prior to fraction 2 and rigidly registered to the fraction 1 CT using the applicator and cervix as landmarks. The bladder, rectum, and sigmoid colon were contoured and the treatment plan for fraction 1 was copied onto the fraction 2 CT. The same procedure was applied for fractions 3 and 4 with a new implant followed by a CT/MR-based plan generated for fraction 3, and an evaluation CT for fraction 4. The absolute interfraction change in EQD2 and cumulative EBRT+BT was calculated using an alpha/beta value of 3; all doses are reported in EQD2. Differences in interfraction variability between IC and IC/IS plans were investigated. The mean HRCTV volume was 17.8cc (8.1-27cc) for IC plans and 32.6cc (19.6-44.4cc) for IC/IS plans. All IC/IS plans had an average fraction of total dwell time of less than 20% in needles. The D2cc for bladder, rectum, and sigmoid were below the soft/hard EMBRACE II guidelines for all plans (80/90Gy, 65/75Gy, 65/75Gy, respectively). The mean single BT fraction D2cc to bladder, rectum, and sigmoid were 7.9Gy, 2.9Gy and 4.2Gy. The bladder D2cc displayed the greatest interfraction variability, with an average absolute interfraction difference of 1.8±1.3Gy, while rectum and sigmoid were 0.6±0.5Gy and 0.7±0.7Gy. Differences between IC and IC/IS plans were also compared. The mean single fraction D2cc to bladder was lower for IC/IS plans (7.2±1.0Gy) as compared to IC plans (8.7±0.4Gy). The mean single fraction D2cc to rectum and sigmoid were similar between the two methods (2.8±0.3Gy and 4.3±0.3Gy for IC/IS versus 2.9±0.3Gy and 4.1±0.3Gy for IC). The absolute interfraction D2cc difference was minimal with both applicators (Figure 1). The interfraction D2cc difference to bladder, rectum, and sigmoid was similar for IC/IS plans (1.8±1.1Gy, 0.6±0.5Gy and 0.7±0.8Gy) as compared to IC plans (1.8±1.4Gy, 0.5±0.4, 0.6±0.7Gy). Overall, the dose to the organs at risk was within the acceptable limits for all fraction plans. The dose differences between the two applicators were minimal, demonstrating that an overnight treatment procedure using IC and IC/IS plans is a viable option.
PO37
目的:单次植入治疗多段宫颈HDR BT,减少了手术的整体包装时间,减少了患者麻醉和放射肿瘤学人员资源。腔内(IC)和腔内/间质(IC/IS)应用器可以在近距离治疗部分之间移动,膀胱和肠道填充可导致OAR剂量测定的交叉变化。单个植入物的干涉剂量变化尚未得到很好的量化,也不清楚是否需要对每个植入物进行适应性的重新计划。方法与材料采用HDR BT治疗的局部晚期宫颈癌患者10例:5例连续IC (T&R涂抹器)和5例连续混合IC/IS (T&R间质针)。每位患者接受45Gy的25份EBRT,随后接受28Gy的4份HDR MR-IGABT,并使用Alatus阴道气囊填充(Radiadyne, Latham, NY)。BT采用双种植技术进行施用。第一次植入后,通过CT和MRI计划和交付第1部分。住院过夜后,在第2部分之前获得新的CT,并使用涂抹器和子宫颈作为标志严格注册到第1部分CT上。勾画膀胱、直肠和乙状结肠的轮廓,将第1部分的治疗方案复制到第2部分的CT上。对第3段和第4段应用相同的程序,植入新的植入物,然后对第3段生成基于CT/ mr的计划,对第4段进行评估CT。使用alpha/beta值3计算EQD2和累积EBRT+BT的绝对干涉变化;所有剂量均在EQD2中报告。研究了IC和IC/IS计划之间的干涉变异性差异。结果IC组HRCTV平均容积为17.8cc (8.1 ~ 27cc), IC/IS组HRCTV平均容积为32.6cc (19.6 ~ 44.4cc)。所有IC/IS方案在针内的平均总停留时间小于20%。膀胱、直肠和乙状结肠的D2cc均低于所有方案的软/硬EMBRACE II指南(分别为80/90Gy、65/75Gy、65/75Gy)。膀胱、直肠和乙状结肠的平均单次BT分数分别为7.9Gy、2.9Gy和4.2Gy。膀胱D2cc表现出最大的干涉变异性,平均绝对干涉差为1.8±1.3Gy,直肠和乙状结肠分别为0.6±0.5Gy和0.7±0.7 gy。还比较了IC和IC/IS方案之间的差异。IC/IS组D2cc到膀胱的平均单次分数(7.2±1.0Gy)低于IC组(8.7±0.4Gy)。两种方法对直肠和乙状结肠的平均单分数D2cc相似(IC/IS组为2.8±0.3Gy和4.3±0.3Gy, IC组为2.9±0.3Gy和4.1±0.3Gy)。两种应用器的绝对干涉D2cc差异最小(图1)。IC/IS方案膀胱、直肠和乙状结肠的干涉D2cc差异(1.8±1.1Gy, 0.6±0.5 gy和0.7±0.8Gy)与IC方案(1.8±1.4Gy, 0.5±0.4 gy, 0.6±0.7 gy)相似。结论总体而言,所有分级方案对有危险器官的剂量均在可接受范围内。两种涂抹器之间的剂量差异很小,表明使用IC和IC/IS计划的过夜治疗程序是可行的选择。单次植入治疗宫颈HDR BT的多个部分,可以减少手术的整体包装时间,减少患者麻醉和放射肿瘤学人员资源,因为减少了生成的计划数量。腔内(IC)和腔内/间质(IC/IS)应用器可以在近距离治疗部分之间移动,膀胱和肠道填充可导致OAR剂量测定的交叉变化。单个植入物的干涉剂量变化尚未得到很好的量化,也不清楚是否需要对每个植入物进行适应性的重新计划。本研究纳入10例局部晚期宫颈癌HDR BT治疗患者:5例连续IC (T&R涂抹器)和5例连续混合IC/IS (T&R间质针)。每位患者接受45Gy的25份EBRT,随后接受28Gy的4份HDR MR-IGABT,并使用Alatus阴道气囊填充(Radiadyne, Latham, NY)。BT采用双种植技术进行施用。第一次植入后,通过CT和MRI计划和交付第1部分。住院过夜后,在第2部分之前获得新的CT,并使用涂抹器和子宫颈作为标志严格注册到第1部分CT上。勾画膀胱、直肠和乙状结肠的轮廓,将第1部分的治疗方案复制到第2部分的CT上。对第3段和第4段应用相同的程序,植入新的植入物,然后对第3段生成基于CT/ mr的计划,对第4段进行评估CT。使用alpha/beta值3计算EQD2和累积EBRT+BT的绝对干涉变化;所有剂量均在EQD2中报告。 研究了IC和IC/IS计划之间的干涉变异性差异。IC计划的平均HRCTV体积为17.8cc (8.1-27cc), IC/IS计划的平均HRCTV体积为32.6cc (19.6-44.4cc)。所有IC/IS方案在针内的平均总停留时间小于20%。膀胱、直肠和乙状结肠的D2cc均低于所有方案的软/硬EMBRACE II指南(分别为80/90Gy、65/75Gy、65/75Gy)。膀胱、直肠和乙状结肠的平均单次BT分数分别为7.9Gy、2.9Gy和4.2Gy。膀胱D2cc表现出最大的干涉变异性,平均绝对干涉差为1.8±1.3Gy,直肠和乙状结肠分别为0.6±0.5Gy和0.7±0.7 gy。还比较了IC和IC/IS方案之间的差异。IC/IS组D2cc到膀胱的平均单次分数(7.2±1.0Gy)低于IC组(8.7±0.4Gy)。两种方法对直肠和乙状结肠的平均单分数D2cc相似(IC/IS组为2.8±0.3Gy和4.3±0.3Gy, IC组为2.9±0.3Gy和4.1±0.3Gy)。两种应用器的绝对干涉D2cc差异最小(图1)。IC/IS方案膀胱、直肠和乙状结肠的干涉D2cc差异(1.8±1.1Gy, 0.6±0.5 gy和0.7±0.8Gy)与IC方案(1.8±1.4Gy, 0.5±0.4 gy, 0.6±0.7 gy)相似。总的来说,对有危险的器官的剂量在所有部分计划的可接受范围内。两种涂抹器之间的剂量差异很小,表明使用IC和IC/IS计划的过夜治疗程序是可行的选择。 研究了IC和IC/IS计划之间的干涉变异性差异。IC计划的平均HRCTV体积为17.8cc (8.1-27cc), IC/IS计划的平均HRCTV体积为32.6cc (19.6-44.4cc)。所有IC/IS方案在针内的平均总停留时间小于20%。膀胱、直肠和乙状结肠的D2cc均低于所有方案的软/硬EMBRACE II指南(分别为80/90Gy、65/75Gy、65/75Gy)。膀胱、直肠和乙状结肠的平均单次BT分数分别为7.9Gy、2.9Gy和4.2Gy。膀胱D2cc表现出最大的干涉变异性,平均绝对干涉差为1.8±1.3Gy,直肠和乙状结肠分别为0.6±0.5Gy和0.7±0.7 gy。还比较了IC和IC/IS方案之间的差异。IC/IS组D2cc到膀胱的平均单次分数(7.2±1.0Gy)低于IC组(8.7±0.4Gy)。两种方法对直肠和乙状结肠的平均单分数D2cc相似(IC/IS组为2.8±0.3Gy和4.3±0.3Gy, IC组为2.9±0.3Gy和4.1±0.3Gy)。两种应用器的绝对干涉D2cc差异最小(图1)。IC/IS方案膀胱、直肠和乙状结肠的干涉D2cc差异(1.8±1.1Gy, 0.6±0.5 gy和0.7±0.8Gy)与IC方案(1.8±1.4Gy, 0.5±0.4 gy, 0.6±0.7 gy)相似。总的来说,对有危险的器官的剂量在所有部分计划的可接受范围内。两种涂抹器之间的剂量差异很小,表明使用IC和IC/IS计划的过夜治疗程序是可行的选择。
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