PO26

Pooja Venkatesh, Juhi Purswani, Nicholas Colangelo, Sofia Perez Otero, Nicole Hindman, Stella Lymberis
{"title":"PO26","authors":"Pooja Venkatesh, Juhi Purswani, Nicholas Colangelo, Sofia Perez Otero, Nicole Hindman, Stella Lymberis","doi":"10.1016/j.brachy.2023.06.127","DOIUrl":null,"url":null,"abstract":"Purpose Radiation toxicity to female erectile tissue, specifically the bulboclitoral apparatus, has not been previously investigated. This retrospective cohort study aims to demonstrate the feasibility of contouring the bulboclitoris (BC) and evaluate dose received by the BC in patients who underwent interstitial gynecologic brachytherapy for tumors involving the lower vagina and periurethral region. Materials and Methods Patients were treated with HDR brachytherapy between the years 2017 and 2022. All patients underwent IMRT external beam radiotherapy (EBRT) to the pelvis and bilateral inguinal region (45 Gy in 25 fractions) followed by High Dose Rate Ir-192 interstitial brachytherapy using the CT/MR M.A.C. Interstitial Gyn Template in 5 fractions for a total dose of 25 Gy (range, 22.5 - 27.5 Gy). The bulboclitoris (BC) was contoured retrospectively by a radiation oncologist and a pelvic radiologist using T2 MRI sequences fused to the pre-treatment and brachytherapy CT simulation. Superiorly, the BC was defined as inferior to the pubic symphysis and attached to the suspensory ligament of the clitoris. Laterally, the crura extend on either side of the corpus. Inferiorly, the vestibular bulbs flank the urethra and vagina on either side and do not extend posteriorly beyond the vagina. A representative contour of the bulboclitoral apparatus is depicted in Figure 1. Dosimetric data for the BC were calculated using EQD2 assuming an alpha-beta ratio of 3 Gy. Median follow up, local control, and vaginal morbidity using CTCAE version 4.0 for vaginal stenosis and pain scoring of the BC was evaluated. Results Patients had a median age of 65 years (range, 49-73). Three of the five patients had a diagnosis of squamous cell carcinoma of the vagina, one patient had recurrent cervical cancer in the vagina, and one patient had endometrioid adenocarcinoma involving the vagina. All tumors were located in the lower vagina, near the BC and urethra. The high-risk clinical target volume (HR-CTV), bladder, rectum, and urethra were contoured on patient imaging during initial treatment planning. Mean D90 of the HR-CTV was 79.82 Gy (range, 72.2-89.9 Gy), mean D2cc to the bladder was 66.54 Gy (range, 50.0-87.2 Gy), mean D2cc to the rectum was 60.9 Gy (range, 46.9-72.9), and mean D0.1cc to the urethra was 79.28 Gy (range, 53.9-93 Gy). At a median follow up of 19.6 months, all patients had a complete local response. One patient had systemic progression and died of metastatic disease. The mean pre-treatment volume of the bulboclitoris was 16.6 cc (range, 11.9 - 20.9 cc) and at brachytherapy was 12.66 cc (range, 7.3 - 22.1 cc). The mean IMRT dose to the BC was 45.87 Gy (range, 44.79 - 46.66 Gy) and mean HDR dose was 14.02 Gy (range, 11.23 - 18.88 Gy). Assuming an alpha-beta ratio of 3 Gy, mean bulboclitoral D90 EQD2 was 62.93 Gy (range of 58.72 to 67.22 Gy). In the acute period, all patients reported severe pain in the clitoral glans region and dysuria that completely resolved after 2 years. Grade 1-2 vaginal stenosis occurred in all patients despite vaginal dilator usage. One patient reported decreased clitoral sensitivity and inability to achieve clitoral-mediated orgasm 5 months after radiotherapy. Conclusions This study demonstrates that contouring the bulboclitoris is feasible and that the BC receives a significant radiation dose during gynecologic brachytherapy which can cause clitoral pain and dysfunction. Further studies are needed to evaluate the dose response of the bulboclitoris as well as explore methods to spare the organ during radiation therapy in order to minimize toxicity and preserve sexual function. Radiation toxicity to female erectile tissue, specifically the bulboclitoral apparatus, has not been previously investigated. This retrospective cohort study aims to demonstrate the feasibility of contouring the bulboclitoris (BC) and evaluate dose received by the BC in patients who underwent interstitial gynecologic brachytherapy for tumors involving the lower vagina and periurethral region. Patients were treated with HDR brachytherapy between the years 2017 and 2022. All patients underwent IMRT external beam radiotherapy (EBRT) to the pelvis and bilateral inguinal region (45 Gy in 25 fractions) followed by High Dose Rate Ir-192 interstitial brachytherapy using the CT/MR M.A.C. Interstitial Gyn Template in 5 fractions for a total dose of 25 Gy (range, 22.5 - 27.5 Gy). The bulboclitoris (BC) was contoured retrospectively by a radiation oncologist and a pelvic radiologist using T2 MRI sequences fused to the pre-treatment and brachytherapy CT simulation. Superiorly, the BC was defined as inferior to the pubic symphysis and attached to the suspensory ligament of the clitoris. Laterally, the crura extend on either side of the corpus. Inferiorly, the vestibular bulbs flank the urethra and vagina on either side and do not extend posteriorly beyond the vagina. A representative contour of the bulboclitoral apparatus is depicted in Figure 1. Dosimetric data for the BC were calculated using EQD2 assuming an alpha-beta ratio of 3 Gy. Median follow up, local control, and vaginal morbidity using CTCAE version 4.0 for vaginal stenosis and pain scoring of the BC was evaluated. Patients had a median age of 65 years (range, 49-73). Three of the five patients had a diagnosis of squamous cell carcinoma of the vagina, one patient had recurrent cervical cancer in the vagina, and one patient had endometrioid adenocarcinoma involving the vagina. All tumors were located in the lower vagina, near the BC and urethra. The high-risk clinical target volume (HR-CTV), bladder, rectum, and urethra were contoured on patient imaging during initial treatment planning. Mean D90 of the HR-CTV was 79.82 Gy (range, 72.2-89.9 Gy), mean D2cc to the bladder was 66.54 Gy (range, 50.0-87.2 Gy), mean D2cc to the rectum was 60.9 Gy (range, 46.9-72.9), and mean D0.1cc to the urethra was 79.28 Gy (range, 53.9-93 Gy). At a median follow up of 19.6 months, all patients had a complete local response. One patient had systemic progression and died of metastatic disease. The mean pre-treatment volume of the bulboclitoris was 16.6 cc (range, 11.9 - 20.9 cc) and at brachytherapy was 12.66 cc (range, 7.3 - 22.1 cc). The mean IMRT dose to the BC was 45.87 Gy (range, 44.79 - 46.66 Gy) and mean HDR dose was 14.02 Gy (range, 11.23 - 18.88 Gy). Assuming an alpha-beta ratio of 3 Gy, mean bulboclitoral D90 EQD2 was 62.93 Gy (range of 58.72 to 67.22 Gy). In the acute period, all patients reported severe pain in the clitoral glans region and dysuria that completely resolved after 2 years. Grade 1-2 vaginal stenosis occurred in all patients despite vaginal dilator usage. One patient reported decreased clitoral sensitivity and inability to achieve clitoral-mediated orgasm 5 months after radiotherapy. This study demonstrates that contouring the bulboclitoris is feasible and that the BC receives a significant radiation dose during gynecologic brachytherapy which can cause clitoral pain and dysfunction. Further studies are needed to evaluate the dose response of the bulboclitoris as well as explore methods to spare the organ during radiation therapy in order to minimize toxicity and preserve sexual function.","PeriodicalId":93914,"journal":{"name":"Brachytherapy","volume":"60 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2023-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"PO26\",\"authors\":\"Pooja Venkatesh, Juhi Purswani, Nicholas Colangelo, Sofia Perez Otero, Nicole Hindman, Stella Lymberis\",\"doi\":\"10.1016/j.brachy.2023.06.127\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Purpose Radiation toxicity to female erectile tissue, specifically the bulboclitoral apparatus, has not been previously investigated. This retrospective cohort study aims to demonstrate the feasibility of contouring the bulboclitoris (BC) and evaluate dose received by the BC in patients who underwent interstitial gynecologic brachytherapy for tumors involving the lower vagina and periurethral region. Materials and Methods Patients were treated with HDR brachytherapy between the years 2017 and 2022. All patients underwent IMRT external beam radiotherapy (EBRT) to the pelvis and bilateral inguinal region (45 Gy in 25 fractions) followed by High Dose Rate Ir-192 interstitial brachytherapy using the CT/MR M.A.C. Interstitial Gyn Template in 5 fractions for a total dose of 25 Gy (range, 22.5 - 27.5 Gy). The bulboclitoris (BC) was contoured retrospectively by a radiation oncologist and a pelvic radiologist using T2 MRI sequences fused to the pre-treatment and brachytherapy CT simulation. Superiorly, the BC was defined as inferior to the pubic symphysis and attached to the suspensory ligament of the clitoris. Laterally, the crura extend on either side of the corpus. Inferiorly, the vestibular bulbs flank the urethra and vagina on either side and do not extend posteriorly beyond the vagina. A representative contour of the bulboclitoral apparatus is depicted in Figure 1. Dosimetric data for the BC were calculated using EQD2 assuming an alpha-beta ratio of 3 Gy. Median follow up, local control, and vaginal morbidity using CTCAE version 4.0 for vaginal stenosis and pain scoring of the BC was evaluated. Results Patients had a median age of 65 years (range, 49-73). Three of the five patients had a diagnosis of squamous cell carcinoma of the vagina, one patient had recurrent cervical cancer in the vagina, and one patient had endometrioid adenocarcinoma involving the vagina. All tumors were located in the lower vagina, near the BC and urethra. The high-risk clinical target volume (HR-CTV), bladder, rectum, and urethra were contoured on patient imaging during initial treatment planning. Mean D90 of the HR-CTV was 79.82 Gy (range, 72.2-89.9 Gy), mean D2cc to the bladder was 66.54 Gy (range, 50.0-87.2 Gy), mean D2cc to the rectum was 60.9 Gy (range, 46.9-72.9), and mean D0.1cc to the urethra was 79.28 Gy (range, 53.9-93 Gy). At a median follow up of 19.6 months, all patients had a complete local response. One patient had systemic progression and died of metastatic disease. The mean pre-treatment volume of the bulboclitoris was 16.6 cc (range, 11.9 - 20.9 cc) and at brachytherapy was 12.66 cc (range, 7.3 - 22.1 cc). The mean IMRT dose to the BC was 45.87 Gy (range, 44.79 - 46.66 Gy) and mean HDR dose was 14.02 Gy (range, 11.23 - 18.88 Gy). Assuming an alpha-beta ratio of 3 Gy, mean bulboclitoral D90 EQD2 was 62.93 Gy (range of 58.72 to 67.22 Gy). In the acute period, all patients reported severe pain in the clitoral glans region and dysuria that completely resolved after 2 years. Grade 1-2 vaginal stenosis occurred in all patients despite vaginal dilator usage. One patient reported decreased clitoral sensitivity and inability to achieve clitoral-mediated orgasm 5 months after radiotherapy. Conclusions This study demonstrates that contouring the bulboclitoris is feasible and that the BC receives a significant radiation dose during gynecologic brachytherapy which can cause clitoral pain and dysfunction. Further studies are needed to evaluate the dose response of the bulboclitoris as well as explore methods to spare the organ during radiation therapy in order to minimize toxicity and preserve sexual function. Radiation toxicity to female erectile tissue, specifically the bulboclitoral apparatus, has not been previously investigated. This retrospective cohort study aims to demonstrate the feasibility of contouring the bulboclitoris (BC) and evaluate dose received by the BC in patients who underwent interstitial gynecologic brachytherapy for tumors involving the lower vagina and periurethral region. Patients were treated with HDR brachytherapy between the years 2017 and 2022. All patients underwent IMRT external beam radiotherapy (EBRT) to the pelvis and bilateral inguinal region (45 Gy in 25 fractions) followed by High Dose Rate Ir-192 interstitial brachytherapy using the CT/MR M.A.C. Interstitial Gyn Template in 5 fractions for a total dose of 25 Gy (range, 22.5 - 27.5 Gy). The bulboclitoris (BC) was contoured retrospectively by a radiation oncologist and a pelvic radiologist using T2 MRI sequences fused to the pre-treatment and brachytherapy CT simulation. Superiorly, the BC was defined as inferior to the pubic symphysis and attached to the suspensory ligament of the clitoris. Laterally, the crura extend on either side of the corpus. Inferiorly, the vestibular bulbs flank the urethra and vagina on either side and do not extend posteriorly beyond the vagina. A representative contour of the bulboclitoral apparatus is depicted in Figure 1. Dosimetric data for the BC were calculated using EQD2 assuming an alpha-beta ratio of 3 Gy. Median follow up, local control, and vaginal morbidity using CTCAE version 4.0 for vaginal stenosis and pain scoring of the BC was evaluated. Patients had a median age of 65 years (range, 49-73). Three of the five patients had a diagnosis of squamous cell carcinoma of the vagina, one patient had recurrent cervical cancer in the vagina, and one patient had endometrioid adenocarcinoma involving the vagina. All tumors were located in the lower vagina, near the BC and urethra. The high-risk clinical target volume (HR-CTV), bladder, rectum, and urethra were contoured on patient imaging during initial treatment planning. Mean D90 of the HR-CTV was 79.82 Gy (range, 72.2-89.9 Gy), mean D2cc to the bladder was 66.54 Gy (range, 50.0-87.2 Gy), mean D2cc to the rectum was 60.9 Gy (range, 46.9-72.9), and mean D0.1cc to the urethra was 79.28 Gy (range, 53.9-93 Gy). At a median follow up of 19.6 months, all patients had a complete local response. One patient had systemic progression and died of metastatic disease. The mean pre-treatment volume of the bulboclitoris was 16.6 cc (range, 11.9 - 20.9 cc) and at brachytherapy was 12.66 cc (range, 7.3 - 22.1 cc). The mean IMRT dose to the BC was 45.87 Gy (range, 44.79 - 46.66 Gy) and mean HDR dose was 14.02 Gy (range, 11.23 - 18.88 Gy). Assuming an alpha-beta ratio of 3 Gy, mean bulboclitoral D90 EQD2 was 62.93 Gy (range of 58.72 to 67.22 Gy). In the acute period, all patients reported severe pain in the clitoral glans region and dysuria that completely resolved after 2 years. Grade 1-2 vaginal stenosis occurred in all patients despite vaginal dilator usage. One patient reported decreased clitoral sensitivity and inability to achieve clitoral-mediated orgasm 5 months after radiotherapy. This study demonstrates that contouring the bulboclitoris is feasible and that the BC receives a significant radiation dose during gynecologic brachytherapy which can cause clitoral pain and dysfunction. Further studies are needed to evaluate the dose response of the bulboclitoris as well as explore methods to spare the organ during radiation therapy in order to minimize toxicity and preserve sexual function.\",\"PeriodicalId\":93914,\"journal\":{\"name\":\"Brachytherapy\",\"volume\":\"60 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.2023.06.127\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Brachytherapy","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1016/j.brachy.2023.06.127","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

目的辐射对女性勃起组织,特别是球阴蒂器官的毒性,以前没有研究过。本回顾性队列研究的目的是证明球囊阴蒂(BC)轮廓化的可行性,并评估接受阴道下段和尿道周围肿瘤间质性妇科近距离放射治疗的患者所接受的BC剂量。材料与方法患者于2017 - 2022年接受HDR近距离放疗。所有患者均接受骨盆和双侧腹股沟区域的IMRT外束放疗(EBRT) (45 Gy,分25次),随后采用CT/MR M.A.C.间质Gyn模板进行高剂量率Ir-192间质近距离放疗,分5次,总剂量为25 Gy(范围22.5 - 27.5 Gy)。由放射肿瘤学家和骨盆放射科医生使用T2 MRI序列融合治疗前和近距离治疗CT模拟对球囊阴蒂(BC)进行回顾性轮廓。上,BC被定义为在耻骨联合下方,附着于阴蒂悬韧带。从侧面看,脚在躯干两侧延伸。在下方,前庭球位于尿道和阴道两侧,不向后延伸到阴道以外。球阴蒂器官的代表性轮廓如图1所示。使用EQD2计算BC的剂量学数据,假设α - β比为3 Gy。使用CTCAE 4.0版本评估阴道狭窄和BC疼痛评分,评估中位随访、局部对照和阴道发病率。结果患者中位年龄为65岁(49-73岁)。5名患者中有3名被诊断为阴道鳞状细胞癌,1名患者患有阴道复发性宫颈癌,1名患者患有累及阴道的子宫内膜样腺癌。所有肿瘤均位于阴道下部,靠近BC和尿道。高危临床靶体积(HR-CTV)、膀胱、直肠和尿道在初始治疗计划期间通过患者成像进行轮廓。HR-CTV平均D90为79.82 Gy(范围:72.2 ~ 89.9 Gy),膀胱平均D2cc为66.54 Gy(范围:50.0 ~ 87.2 Gy),直肠平均D2cc为60.9 Gy(范围:46.9 ~ 72.9),尿道平均D0.1cc为79.28 Gy(范围:53.9 ~ 93 Gy)。在中位19.6个月的随访中,所有患者都有完全的局部缓解。一名患者出现全身进展并死于转移性疾病。球阴蒂治疗前平均体积为16.6 cc(范围,11.9 - 20.9 cc),近距离治疗时平均体积为12.66 cc(范围,7.3 - 22.1 cc)。对BC的平均IMRT剂量为45.87 Gy(范围,44.79 ~ 46.66 Gy),平均HDR剂量为14.02 Gy(范围,11.23 ~ 18.88 Gy)。假设α - β比值为3 Gy,球阴蒂平均D90 EQD2为62.93 Gy(范围为58.72 ~ 67.22 Gy)。在急性期,所有患者均报告阴蒂头区剧烈疼痛和排尿困难,2年后完全缓解。尽管使用了阴道扩张器,但所有患者仍发生1-2级阴道狭窄。一名患者报告放疗后5个月阴蒂敏感性下降,无法达到阴蒂介导性高潮。结论在妇科近距离放射治疗中,阴蒂包膜是可行的,而阴蒂包膜受到的辐射剂量较大,可引起阴蒂疼痛和功能障碍。需要进一步的研究来评估球阴蒂的剂量反应,并探索在放射治疗中保留该器官的方法,以尽量减少毒性并保持性功能。辐射对女性勃起组织的毒性,特别是球阴蒂器官,以前没有研究过。本回顾性队列研究的目的是证明球囊阴蒂(BC)轮廓化的可行性,并评估接受阴道下段和尿道周围肿瘤间质性妇科近距离放射治疗的患者所接受的BC剂量。患者在2017年至2022年期间接受HDR近距离放疗。所有患者均接受骨盆和双侧腹股沟区域的IMRT外束放疗(EBRT) (45 Gy,分25次),随后采用CT/MR M.A.C.间质Gyn模板进行高剂量率Ir-192间质近距离放疗,分5次,总剂量为25 Gy(范围22.5 - 27.5 Gy)。由放射肿瘤学家和骨盆放射科医生使用T2 MRI序列融合治疗前和近距离治疗CT模拟对球囊阴蒂(BC)进行回顾性轮廓。上,BC被定义为在耻骨联合下方,附着于阴蒂悬韧带。从侧面看,脚在躯干两侧延伸。在下方,前庭球位于尿道和阴道两侧,不向后延伸到阴道以外。 球阴蒂器官的代表性轮廓如图1所示。使用EQD2计算BC的剂量学数据,假设α - β比为3 Gy。使用CTCAE 4.0版本评估阴道狭窄和BC疼痛评分,评估中位随访、局部对照和阴道发病率。患者的中位年龄为65岁(49-73岁)。5名患者中有3名被诊断为阴道鳞状细胞癌,1名患者患有阴道复发性宫颈癌,1名患者患有累及阴道的子宫内膜样腺癌。所有肿瘤均位于阴道下部,靠近BC和尿道。高危临床靶体积(HR-CTV)、膀胱、直肠和尿道在初始治疗计划期间通过患者成像进行轮廓。HR-CTV平均D90为79.82 Gy(范围:72.2 ~ 89.9 Gy),膀胱平均D2cc为66.54 Gy(范围:50.0 ~ 87.2 Gy),直肠平均D2cc为60.9 Gy(范围:46.9 ~ 72.9),尿道平均D0.1cc为79.28 Gy(范围:53.9 ~ 93 Gy)。在中位19.6个月的随访中,所有患者都有完全的局部缓解。一名患者出现全身进展并死于转移性疾病。球阴蒂治疗前平均体积为16.6 cc(范围,11.9 - 20.9 cc),近距离治疗时平均体积为12.66 cc(范围,7.3 - 22.1 cc)。对BC的平均IMRT剂量为45.87 Gy(范围,44.79 ~ 46.66 Gy),平均HDR剂量为14.02 Gy(范围,11.23 ~ 18.88 Gy)。假设α - β比值为3 Gy,球阴蒂平均D90 EQD2为62.93 Gy(范围为58.72 ~ 67.22 Gy)。在急性期,所有患者均报告阴蒂头区剧烈疼痛和排尿困难,2年后完全缓解。尽管使用了阴道扩张器,但所有患者仍发生1-2级阴道狭窄。一名患者报告放疗后5个月阴蒂敏感性下降,无法达到阴蒂介导性高潮。本研究表明,轮廓球阴蒂是可行的,并且BC在妇科近距离放射治疗中接受显著的辐射剂量,可引起阴蒂疼痛和功能障碍。需要进一步的研究来评估球阴蒂的剂量反应,并探索在放射治疗中保留该器官的方法,以尽量减少毒性并保持性功能。 球阴蒂器官的代表性轮廓如图1所示。使用EQD2计算BC的剂量学数据,假设α - β比为3 Gy。使用CTCAE 4.0版本评估阴道狭窄和BC疼痛评分,评估中位随访、局部对照和阴道发病率。患者的中位年龄为65岁(49-73岁)。5名患者中有3名被诊断为阴道鳞状细胞癌,1名患者患有阴道复发性宫颈癌,1名患者患有累及阴道的子宫内膜样腺癌。所有肿瘤均位于阴道下部,靠近BC和尿道。高危临床靶体积(HR-CTV)、膀胱、直肠和尿道在初始治疗计划期间通过患者成像进行轮廓。HR-CTV平均D90为79.82 Gy(范围:72.2 ~ 89.9 Gy),膀胱平均D2cc为66.54 Gy(范围:50.0 ~ 87.2 Gy),直肠平均D2cc为60.9 Gy(范围:46.9 ~ 72.9),尿道平均D0.1cc为79.28 Gy(范围:53.9 ~ 93 Gy)。在中位19.6个月的随访中,所有患者都有完全的局部缓解。一名患者出现全身进展并死于转移性疾病。球阴蒂治疗前平均体积为16.6 cc(范围,11.9 - 20.9 cc),近距离治疗时平均体积为12.66 cc(范围,7.3 - 22.1 cc)。对BC的平均IMRT剂量为45.87 Gy(范围,44.79 ~ 46.66 Gy),平均HDR剂量为14.02 Gy(范围,11.23 ~ 18.88 Gy)。假设α - β比值为3 Gy,球阴蒂平均D90 EQD2为62.93 Gy(范围为58.72 ~ 67.22 Gy)。在急性期,所有患者均报告阴蒂头区剧烈疼痛和排尿困难,2年后完全缓解。尽管使用了阴道扩张器,但所有患者仍发生1-2级阴道狭窄。一名患者报告放疗后5个月阴蒂敏感性下降,无法达到阴蒂介导性高潮。本研究表明,轮廓球阴蒂是可行的,并且BC在妇科近距离放射治疗中接受显著的辐射剂量,可引起阴蒂疼痛和功能障碍。需要进一步的研究来评估球阴蒂的剂量反应,并探索在放射治疗中保留该器官的方法,以尽量减少毒性并保持性功能。
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PO26
Purpose Radiation toxicity to female erectile tissue, specifically the bulboclitoral apparatus, has not been previously investigated. This retrospective cohort study aims to demonstrate the feasibility of contouring the bulboclitoris (BC) and evaluate dose received by the BC in patients who underwent interstitial gynecologic brachytherapy for tumors involving the lower vagina and periurethral region. Materials and Methods Patients were treated with HDR brachytherapy between the years 2017 and 2022. All patients underwent IMRT external beam radiotherapy (EBRT) to the pelvis and bilateral inguinal region (45 Gy in 25 fractions) followed by High Dose Rate Ir-192 interstitial brachytherapy using the CT/MR M.A.C. Interstitial Gyn Template in 5 fractions for a total dose of 25 Gy (range, 22.5 - 27.5 Gy). The bulboclitoris (BC) was contoured retrospectively by a radiation oncologist and a pelvic radiologist using T2 MRI sequences fused to the pre-treatment and brachytherapy CT simulation. Superiorly, the BC was defined as inferior to the pubic symphysis and attached to the suspensory ligament of the clitoris. Laterally, the crura extend on either side of the corpus. Inferiorly, the vestibular bulbs flank the urethra and vagina on either side and do not extend posteriorly beyond the vagina. A representative contour of the bulboclitoral apparatus is depicted in Figure 1. Dosimetric data for the BC were calculated using EQD2 assuming an alpha-beta ratio of 3 Gy. Median follow up, local control, and vaginal morbidity using CTCAE version 4.0 for vaginal stenosis and pain scoring of the BC was evaluated. Results Patients had a median age of 65 years (range, 49-73). Three of the five patients had a diagnosis of squamous cell carcinoma of the vagina, one patient had recurrent cervical cancer in the vagina, and one patient had endometrioid adenocarcinoma involving the vagina. All tumors were located in the lower vagina, near the BC and urethra. The high-risk clinical target volume (HR-CTV), bladder, rectum, and urethra were contoured on patient imaging during initial treatment planning. Mean D90 of the HR-CTV was 79.82 Gy (range, 72.2-89.9 Gy), mean D2cc to the bladder was 66.54 Gy (range, 50.0-87.2 Gy), mean D2cc to the rectum was 60.9 Gy (range, 46.9-72.9), and mean D0.1cc to the urethra was 79.28 Gy (range, 53.9-93 Gy). At a median follow up of 19.6 months, all patients had a complete local response. One patient had systemic progression and died of metastatic disease. The mean pre-treatment volume of the bulboclitoris was 16.6 cc (range, 11.9 - 20.9 cc) and at brachytherapy was 12.66 cc (range, 7.3 - 22.1 cc). The mean IMRT dose to the BC was 45.87 Gy (range, 44.79 - 46.66 Gy) and mean HDR dose was 14.02 Gy (range, 11.23 - 18.88 Gy). Assuming an alpha-beta ratio of 3 Gy, mean bulboclitoral D90 EQD2 was 62.93 Gy (range of 58.72 to 67.22 Gy). In the acute period, all patients reported severe pain in the clitoral glans region and dysuria that completely resolved after 2 years. Grade 1-2 vaginal stenosis occurred in all patients despite vaginal dilator usage. One patient reported decreased clitoral sensitivity and inability to achieve clitoral-mediated orgasm 5 months after radiotherapy. Conclusions This study demonstrates that contouring the bulboclitoris is feasible and that the BC receives a significant radiation dose during gynecologic brachytherapy which can cause clitoral pain and dysfunction. Further studies are needed to evaluate the dose response of the bulboclitoris as well as explore methods to spare the organ during radiation therapy in order to minimize toxicity and preserve sexual function. Radiation toxicity to female erectile tissue, specifically the bulboclitoral apparatus, has not been previously investigated. This retrospective cohort study aims to demonstrate the feasibility of contouring the bulboclitoris (BC) and evaluate dose received by the BC in patients who underwent interstitial gynecologic brachytherapy for tumors involving the lower vagina and periurethral region. Patients were treated with HDR brachytherapy between the years 2017 and 2022. All patients underwent IMRT external beam radiotherapy (EBRT) to the pelvis and bilateral inguinal region (45 Gy in 25 fractions) followed by High Dose Rate Ir-192 interstitial brachytherapy using the CT/MR M.A.C. Interstitial Gyn Template in 5 fractions for a total dose of 25 Gy (range, 22.5 - 27.5 Gy). The bulboclitoris (BC) was contoured retrospectively by a radiation oncologist and a pelvic radiologist using T2 MRI sequences fused to the pre-treatment and brachytherapy CT simulation. Superiorly, the BC was defined as inferior to the pubic symphysis and attached to the suspensory ligament of the clitoris. Laterally, the crura extend on either side of the corpus. Inferiorly, the vestibular bulbs flank the urethra and vagina on either side and do not extend posteriorly beyond the vagina. A representative contour of the bulboclitoral apparatus is depicted in Figure 1. Dosimetric data for the BC were calculated using EQD2 assuming an alpha-beta ratio of 3 Gy. Median follow up, local control, and vaginal morbidity using CTCAE version 4.0 for vaginal stenosis and pain scoring of the BC was evaluated. Patients had a median age of 65 years (range, 49-73). Three of the five patients had a diagnosis of squamous cell carcinoma of the vagina, one patient had recurrent cervical cancer in the vagina, and one patient had endometrioid adenocarcinoma involving the vagina. All tumors were located in the lower vagina, near the BC and urethra. The high-risk clinical target volume (HR-CTV), bladder, rectum, and urethra were contoured on patient imaging during initial treatment planning. Mean D90 of the HR-CTV was 79.82 Gy (range, 72.2-89.9 Gy), mean D2cc to the bladder was 66.54 Gy (range, 50.0-87.2 Gy), mean D2cc to the rectum was 60.9 Gy (range, 46.9-72.9), and mean D0.1cc to the urethra was 79.28 Gy (range, 53.9-93 Gy). At a median follow up of 19.6 months, all patients had a complete local response. One patient had systemic progression and died of metastatic disease. The mean pre-treatment volume of the bulboclitoris was 16.6 cc (range, 11.9 - 20.9 cc) and at brachytherapy was 12.66 cc (range, 7.3 - 22.1 cc). The mean IMRT dose to the BC was 45.87 Gy (range, 44.79 - 46.66 Gy) and mean HDR dose was 14.02 Gy (range, 11.23 - 18.88 Gy). Assuming an alpha-beta ratio of 3 Gy, mean bulboclitoral D90 EQD2 was 62.93 Gy (range of 58.72 to 67.22 Gy). In the acute period, all patients reported severe pain in the clitoral glans region and dysuria that completely resolved after 2 years. Grade 1-2 vaginal stenosis occurred in all patients despite vaginal dilator usage. One patient reported decreased clitoral sensitivity and inability to achieve clitoral-mediated orgasm 5 months after radiotherapy. This study demonstrates that contouring the bulboclitoris is feasible and that the BC receives a significant radiation dose during gynecologic brachytherapy which can cause clitoral pain and dysfunction. Further studies are needed to evaluate the dose response of the bulboclitoris as well as explore methods to spare the organ during radiation therapy in order to minimize toxicity and preserve sexual function.
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