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Caudally directed posterior high-dose-rate brachytherapy for reirradiation of para-aortic lymph node recurrence: A technical innovation enabled by interventional radiology. 尾侧定向后置高剂量率近距离放疗用于主动脉旁淋巴结复发的再照射:介入放射学的技术创新。
IF 1.8 Pub Date : 2025-12-16 DOI: 10.1016/j.brachy.2025.11.008
Kae Okuma, Yasuaki Arai, Mizuki Ozawa, Hiroki Nakayama, Hiroyuki Okamoto, Ayaka Nagao, Koji Inaba, Tairo Kashihara, Kana Takahashi, Madoka Sakuramachi, Akane Yoshiba, Hiroshi Igaki

Purpose: Reirradiation for para-aortic lymph node (PALN) recurrence is technically challenging due to prior radiation exposure and the anatomical proximity of critical organs such as the small intestine and kidneys, making external beam radiation therapy (EBRT) difficult or unfeasible. High-dose-rate interstitial brachytherapy (HDR-IBT) offers a highly localized treatment alternative; however, it requires precise applicator placement to ensure safety and efficacy.

Methods and materials: We report a case of PALN recurrence located between the aorta and inferior vena cava (IVC) in a patient previously treated with multiple courses of EBRT. Due to the lesion's high-risk location and prior irradiation, further EBRT was not a viable option. In collaboration with interventional radiologists, a novel posterior paravertebral approach was adopted. Under fluoroscopic and computed tomography (CT) guidance, a 17 G percutaneous transhepatic cholangiography (PTC) needle was inserted from the patient's back. The guidewire was advanced through the psoas muscle and intentionally redirected caudally at an angle of nearly 90 degrees to avoid major vascular structures. Following tract dilation using a ureteral balloon and dilator system, a flexible brachytherapy applicator was inserted and fixed in place. The patient received six fractions of 5 Gy (total dose: 30 Gy), with the applicator maintained in situ throughout the treatment period.

Results: The treatment was completed without any adverse events. CT imaging at 4 months post-treatment showed tumor shrinkage and reduced contrast enhancement. No radiation-related toxicities were observed during or after treatment. Local control has been maintained for over 4 years.

Conclusions: This case demonstrates the feasibility and safety of fractionated HDR-IBT for reirradiation of deeply located PALN recurrence in a previously irradiated field. While single-fraction HDR-IBT can be performed via a direct posterior approach, fractionated treatment requires stable applicator placement over several days. To mitigate the risk of vascular injury due to applicator displacement, precise angulation of the insertion trajectory was critical. This report highlights how interdisciplinary collaboration enabled accurate, vessel-sparing needle placement, providing a minimally invasive and effective treatment option for patients with PALN recurrence who are not candidates for further EBRT.

目的:主动脉旁淋巴结(PALN)复发的再放射治疗在技术上具有挑战性,因为先前的放射暴露和小肠和肾脏等关键器官的解剖邻近,使得外束放射治疗(EBRT)困难或不可行。高剂量率间质近距离放射治疗(HDR-IBT)提供了一种高度局部化的治疗选择;然而,它需要精确的涂抹器放置,以确保安全性和有效性。方法和材料:我们报告了一个位于主动脉和下腔静脉(IVC)之间的PALN复发病例,该患者先前接受过多个疗程的EBRT治疗。由于病变的高危位置和先前的放疗,进一步的EBRT不是一个可行的选择。在与介入放射科医师的合作下,采用了一种新的椎旁后路入路。在透视和CT引导下,从患者背部插入17 G经皮经肝胆管造影(PTC)针。导丝通过腰肌向前推进,并有意以近90度的角度向尾端重新定向,以避开主要的血管结构。使用输尿管球囊和扩张器系统进行尿道扩张后,插入并固定一个灵活的近距离治疗涂药器。患者接受5 Gy的六个分量(总剂量:30 Gy),整个治疗期间涂抹器保持原位。结果:治疗完成,无不良事件发生。治疗后4个月CT显示肿瘤缩小,对比增强减弱。在治疗期间或治疗后未观察到与辐射相关的毒性。当地控制已维持了4年多。结论:本病例证明了分级HDR-IBT在既往放疗区深部复发PALN再照射的可行性和安全性。单段式HDR-IBT可以通过直接后路入路进行,而分段式治疗需要数天内稳定的涂抹器放置。为了减少由于涂抹器移位造成血管损伤的风险,插入轨迹的精确角度至关重要。该报告强调了跨学科合作如何实现准确,保留血管的针头放置,为不适合进一步EBRT的PALN复发患者提供微创和有效的治疗选择。
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引用次数: 0
Evaluation of AI chatbot responses to brachytherapy frequently asked questions. 人工智能聊天机器人对近距离治疗常见问题的反应评估。
IF 1.8 Pub Date : 2025-12-16 DOI: 10.1016/j.brachy.2025.10.005
Ramez Kouzy, Ibrahim Ibrahim, Paul Nemr, Saketh Vinjamuri, Bassam Ballout, Juan Sebastian Gonzalez Gonzalez Diaz, Dalissa Negron Figueroa, Molly B El Alam, Zakaria El Kouzi, Comron Hassanzadeh, Osama Mohamad, Chris Weil, Lauren Colbert, Ann Klopp

Purpose: Patients are increasingly using artificial intelligence (AI) chatbots for health information. Evaluating their reliability for specialized topics, such as brachytherapy, is crucial for guiding their safe use. We assessed a readily accessible AI chatbot's suitability for answering frequently asked questions (FAQ) related to brachytherapy.

Methods: We compared responses from an AI chatbot (ChatGPT 4o-mini) against gold standard (GS) authoritative sources for 10 brachytherapy frequently asked questions. Four blinded board-certified brachytherapy experts evaluated 80 response pairs using metrics, including accuracy, clinical appropriateness, readability, and tone. Five simulated patient personas with varying literacy levels were used to assess helpfulness, readability, and emotional tone. The objective readability metrics were also calculated.

Results: Experts rated the AI chatbot higher for accuracy (75% highly/mostly accurate vs. 50% for GS) and appropriateness (77% vs 55%), although inaccuracies were noted in both sources in a blinded review. Simulated patients preferred GS responses (62% vs. 34%), particularly lower-literacy personas, citing better perceived readability (92% easy/very easy vs. 44% for AI) and a more reassuring tone (42% vs. 24% for AI). Objective analysis confirmed that both sources significantly exceeded the recommended reading levels (e.g., >12th grade Flesch-Kincaid), with AI responses being substantially longer. Performance varied considerably across individual questions for both AI and GS sources.

Conclusions: In this blinded cross-sectional evaluation, a publicly available AI chatbot provided accurate responses to brachytherapy-related FAQs. However, further development and validation focused on accessibility, trustworthiness, and user-centered design are required before these tools can be safely and effectively integrated into patient-care workflows.

目的:患者越来越多地使用人工智能(AI)聊天机器人获取健康信息。评估它们在专业领域的可靠性,如近距离治疗,对于指导它们的安全使用至关重要。我们评估了一个易于访问的人工智能聊天机器人在回答与近距离治疗相关的常见问题(FAQ)方面的适用性。方法:我们比较了人工智能聊天机器人(ChatGPT 40 -mini)和金标准(GS)权威来源对10个近距离治疗常见问题的回答。四名盲法委员会认证的近距离治疗专家使用指标评估了80对反应,包括准确性、临床适当性、可读性和语气。五个不同文化水平的模拟病人角色被用来评估帮助,可读性和情绪基调。还计算了客观可读性指标。结果:专家对人工智能聊天机器人的准确性(75%高度/大部分准确,而GS为50%)和适当性(77% 对55%)的评价更高,尽管在一项盲法评价中,两个来源都指出了不准确性。模拟患者更喜欢GS反应(62% vs。34%),尤其是低文化水平的角色,他们认为更容易理解(92%的人认为容易/非常容易,而人工智能的人认为容易/非常容易,这一比例为44%),而且语气更让人放心(42%的人认为 对44%的人认为AI更容易)。24%为人工智能)。客观分析证实,这两个来源都明显超过了推荐的阅读水平(例如,12年级的Flesch-Kincaid),人工智能的反应时间也长得多。AI和GS资源在单个问题上的表现差异很大。结论:在这项盲法横断面评估中,一个公开的人工智能聊天机器人对近距离治疗相关的常见问题提供了准确的回答。然而,在这些工具能够安全有效地集成到患者护理工作流程之前,需要进一步开发和验证可访问性、可信度和以用户为中心的设计。
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引用次数: 0
Low dose iodine-125 brachytherapy and transpupillary thermal therapy for small- to medium-sized choroidal melanoma. 小剂量碘-125近距离治疗和上乳头热治疗中小脉络膜黑色素瘤。
IF 1.8 Pub Date : 2025-12-16 DOI: 10.1016/j.brachy.2025.11.011
S Fattahi, C L Deufel, K V Astafurov, T W Olsen, S L Stafford, M A Neben Wittich, W S Harmsen, J K Viehman, L A Dalvin, I A Petersen, K S Corbin

Purpose: COMS established iodine-125 (125I) brachytherapy as standard of care for medium-sized choroidal melanomas. However, there remains a gap in the literature regarding reduced dosing for medium-sized choroidal melanomas and standard dosing for small-sized choroidal melanomas. We explored the impact of reduced dose 125I brachytherapy on local tumor control and ocular adverse events (AEs).

Methods: Patients diagnosed 2005-2019 with choroidal melanoma <5 mm thick and managed with 125I brachytherapy dose of 65 Gy to depth of 5 mm were included. Dose metrics were calculated using Monte Carlo-based dosimetry. Kaplan-Meier method was used to estimate overall survival and radiation-related AEs. Distant metastasis and local recurrence were reported using cumulative incidence with death as a competing risk. Univariate and multivariate associations were analyzed using Cox proportional hazards regression.

Results: 143 patients met inclusion criteria with median follow-up of 7 years. Five-year Kaplan-Meier estimates of ocular AEs were 59.6% radiation maculopathy, 42.0% cystoid macular edema, 55.2% nonproliferative radiation retinopathy, 10.8% proliferative radiation retinopathy, and 35.6% radiation papillopathy. Five-year cumulative incidence of local recurrence was 0%, 5-year cumulative incidence of distant metastasis was 6.1%, and 5-year Kaplan-Meier estimate of overall survival was 96.5%.

Conclusion: Reduced dose 125I brachytherapy is feasible with excellent local tumor control.

目的:COMS建立碘-125 (125I)近距离放疗作为中等脉络膜黑色素瘤的标准治疗。然而,关于中型脉络膜黑色素瘤的减少剂量和小型脉络膜黑色素瘤的标准剂量,文献中仍然存在空白。我们探讨了低剂量125I近距离放疗对局部肿瘤控制和眼部不良事件(ae)的影响。方法:纳入2005-2019年诊断为脉络膜黑色素瘤的患者,125I近距离放疗剂量为65 Gy,深度为5 mm。剂量计量采用蒙特卡罗剂量法计算。Kaplan-Meier法用于估计总生存率和辐射相关ae。远处转移和局部复发的报道使用累积发病率与死亡作为竞争风险。采用Cox比例风险回归分析单因素和多因素相关性。结果:143例患者符合纳入标准,中位随访7年。五年Kaplan-Meier估计眼部ae为59.6%的放射性黄斑病变,42.0%的囊状黄斑水肿,55.2%的非增殖性放射性视网膜病变,10.8%的增殖性放射性视网膜病变和35.6%的放射性乳头病变。5年累积局部复发发生率为0%,5年累积远处转移发生率为6.1%,5年Kaplan-Meier估计总生存率为96.5%。结论:125I小剂量近距离放疗可行,局部肿瘤控制良好。
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引用次数: 0
Dosimetric impact of androgen deprivation therapy (ADT)-induced prostate deformation in low-dose-rate prostate brachytherapy. 低剂量率前列腺近距离放射治疗中雄激素剥夺疗法(ADT)诱导前列腺变形的剂量学影响。
IF 1.8 Pub Date : 2025-12-16 DOI: 10.1016/j.brachy.2025.11.006
Younghun Yoon, Wooshik Kim, Han-Back Shin, Jihun Kim, Jaeho Cho

Purpose: Androgen deprivation therapy (ADT) for prostate cancer typically reduces prostate volume. This study investigated how the timing of ADT relative to low-dose-rate (LDR) brachytherapy influences the resulting dosimetric outcomes.

Methods: Using deformable image registration and principal component analysis on pre- and post-ADT magnetic resonance images of 34 patients, we developed a statistical model of ADT-induced prostate deformation. We applied this model to 30 low-dose-rate (LDR) brachytherapy plans (prescription dose: 145 Gy) to simulate seed displacement and dose distribution changes from prostate shrinkage. Prostate deformation over time post-ADT was categorized into early, linear, and late response phases. Dosimetric outcomes were analyzed across scenarios with varying prostate volume reduction magnitudes and different intervals between ADT initiation and brachytherapy.

Results: When ADT was initiated concurrently with brachytherapy, the model predicted substantial dose escalation if prostate shrinkage occurred early (prostate D90 ∼206 Gy; urethral V200 ∼47.7%) compared to late shrinkage response (D90 ∼183 Gy; V200 ∼7.1%). In contrast, separating the treatments in time greatly mitigated this effect. For example, assuming early response, performing brachytherapy 3 months before ADT yielded a prostate D90 of ∼183.0 Gy (urethral V200 ∼7.7%), while delaying brachytherapy to 3 months after ADT yielded a D90 of ∼177.8 Gy (V200 ∼1.2%).

Conclusions: Dosimetric analysis showed that greater prostate volume reduction, early ADT response, and concurrent ADT all corresponded to substantially increased doses to the prostate and urethra. Clinically, these findings underscore the importance of carefully planning the timing of ADT relative to brachytherapy to optimize target coverage and minimize unintended dose escalation to normal tissues.

目的:前列腺癌的雄激素剥夺治疗(ADT)通常会减少前列腺体积。本研究调查了相对于低剂量率(LDR)近距离放射治疗的ADT时间如何影响剂量学结果。方法:对34例adt前后的磁共振图像进行形变配准和主成分分析,建立adt致前列腺形变的统计模型。我们将该模型应用于30个低剂量率(LDR)近距离治疗方案(处方剂量:145 Gy),以模拟前列腺萎缩引起的种子位移和剂量分布变化。前列腺变形随adt后时间的变化分为早期、线性和晚期反应阶段。剂量学结果分析了不同前列腺体积缩小程度和ADT开始和近距离治疗之间不同间隔的情况。结果:当ADT与近距离治疗同时开始时,与晚期收缩反应(D90 ~ 183 Gy; V200 ~ 7.1%)相比,如果前列腺收缩早期发生(前列腺D90 ~ 206 Gy;尿道V200 ~ 47.7%),该模型预测剂量会大幅上升。相比之下,及时分离处理大大减轻了这种影响。例如,假设早期反应,在ADT前3个月进行近距离治疗,前列腺D90为~ 183.0 Gy(尿道V200 ~ 7.7%),而延迟至ADT后3个月进行近距离治疗,D90为~ 177.8 Gy (V200 ~ 1.2%)。结论:剂量学分析显示,前列腺体积缩小更大,ADT反应更早,ADT同时发生,均与前列腺和尿道剂量的显著增加相对应。在临床上,这些发现强调了精心规划相对于近距离治疗的ADT时间的重要性,以优化靶覆盖并最小化对正常组织的意外剂量增加。
{"title":"Dosimetric impact of androgen deprivation therapy (ADT)-induced prostate deformation in low-dose-rate prostate brachytherapy.","authors":"Younghun Yoon, Wooshik Kim, Han-Back Shin, Jihun Kim, Jaeho Cho","doi":"10.1016/j.brachy.2025.11.006","DOIUrl":"https://doi.org/10.1016/j.brachy.2025.11.006","url":null,"abstract":"<p><strong>Purpose: </strong>Androgen deprivation therapy (ADT) for prostate cancer typically reduces prostate volume. This study investigated how the timing of ADT relative to low-dose-rate (LDR) brachytherapy influences the resulting dosimetric outcomes.</p><p><strong>Methods: </strong>Using deformable image registration and principal component analysis on pre- and post-ADT magnetic resonance images of 34 patients, we developed a statistical model of ADT-induced prostate deformation. We applied this model to 30 low-dose-rate (LDR) brachytherapy plans (prescription dose: 145 Gy) to simulate seed displacement and dose distribution changes from prostate shrinkage. Prostate deformation over time post-ADT was categorized into early, linear, and late response phases. Dosimetric outcomes were analyzed across scenarios with varying prostate volume reduction magnitudes and different intervals between ADT initiation and brachytherapy.</p><p><strong>Results: </strong>When ADT was initiated concurrently with brachytherapy, the model predicted substantial dose escalation if prostate shrinkage occurred early (prostate D90 ∼206 Gy; urethral V200 ∼47.7%) compared to late shrinkage response (D90 ∼183 Gy; V200 ∼7.1%). In contrast, separating the treatments in time greatly mitigated this effect. For example, assuming early response, performing brachytherapy 3 months before ADT yielded a prostate D90 of ∼183.0 Gy (urethral V200 ∼7.7%), while delaying brachytherapy to 3 months after ADT yielded a D90 of ∼177.8 Gy (V200 ∼1.2%).</p><p><strong>Conclusions: </strong>Dosimetric analysis showed that greater prostate volume reduction, early ADT response, and concurrent ADT all corresponded to substantially increased doses to the prostate and urethra. Clinically, these findings underscore the importance of carefully planning the timing of ADT relative to brachytherapy to optimize target coverage and minimize unintended dose escalation to normal tissues.</p>","PeriodicalId":93914,"journal":{"name":"Brachytherapy","volume":" ","pages":""},"PeriodicalIF":1.8,"publicationDate":"2025-12-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145776823","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
A first-in-human randomized clinical trial of graphics processing units based multi-criteria optimization (gMCO) versus IPSA in high-dose-rate prostate brachytherapy. 基于图形处理单元的多标准优化(gMCO)与IPSA在高剂量率前列腺近距离治疗中的首次人体随机临床试验。
IF 1.8 Pub Date : 2025-12-15 DOI: 10.1016/j.brachy.2025.11.009
F Lacroix, E Poulin, C Bélanger, S Aubin, D Carignan, E Vigneault, A-G Martin, F Bachand, L Beaulieu, W Foster

Purpose: The purpose of this work, a first-in-human randomized clinical trial, was to compare gMCO, a GPU-based multi criteria optimization (MCO) algorithm, to reference plans in terms of planning time and plan quality for prostate HDR brachytherapy.

Methods and materials: The brachytherapy procedure was as follows: (1) Patient installation, (2) Catheter implantation under transrectal ultrasound (US) guidance, (3) 3D US scan, (4) Contouring/catheter reconstruction on Oncentra Prostate (Elekta, Veenendaal, Netherlands), (5) Planning, (6) Treatment. Planning (step 5) was performed, after randomization, using either IPSA (Oncentra Prostate, Veenendaal, Netherlands) or gMCO. The planning times on IPSA or gMCO were recorded. Patients previously had a planning MR in order to identify whether a gross tumor volume (GTV, PIRADS 3 and above) was visible and, if present, the GTV was boosted to a minimum of 19 Gy of the prescription dose. Fifty-five patients were accrued and distributed randomly between both treatment arms. Dosimetric indices (Prostate V100, V150, V200, GTV D90, Urethra D10, Rectum and Bladder V75 and D1cc) of gMCO and Inverse-Planning Simulated Annealing algorithm (IPSA) plans were compared to determine if plan quality and planning times were statistically different.

Results: Results show that the optimization time is reduced by half when using gMCO as compared to IPSA, going from 10-5.2 minutes. Although no statistically significant difference is present between gMCO and IPSA plans when comparing pairs of individual dosimetric indices, gMCO plans exhibit a higher pass rate (higher by a factor ranging from 1.3 to 1.6), as compared to IPSA, when considering a basket of dosimetric indices simultaneously.

Conclusion: The use of gMCO halves the planning time for prostate HDR brachytherapy as compared to IPSA, without decreasing plan quality. The overall gain in efficiency related to the planning process has led to the use of gMCO for all of our HDR prostate cases.

目的:本工作是一项首次人体随机临床试验,目的是比较gMCO,一种基于gpu的多标准优化(MCO)算法,在前列腺HDR近距离治疗的计划时间和计划质量方面与参考计划。方法与材料:近距离治疗流程如下:(1)患者安装,(2)经直肠超声引导下置管,(3)三维超声扫描,(4)Oncentra前列腺(Elekta, Veenendaal,荷兰)轮廓/导管重建,(5)规划,(6)治疗。随机化后进行计划(步骤5),使用IPSA (Oncentra前列腺,Veenendaal,荷兰)或gMCO。记录IPSA或gMCO的规划时间。患者先前进行计划MR以确定是否可见总肿瘤体积(GTV, PIRADS 3及以上),如果存在,将GTV提高到处方剂量的至少19 Gy。55名患者被随机分配到两个治疗组。比较gMCO和逆规划模拟退火算法(reverse - planning Simulated退火算法,IPSA)方案的剂量学指标(前列腺V100、V150、V200、GTV D90、尿道D10、直肠和膀胱V75、D1cc),判断方案质量和计划时间是否有统计学差异。结果:与IPSA相比,gMCO的优化时间缩短了一半,为10-5.2分钟。虽然gMCO计划和IPSA计划在比较个别剂量学指数对时没有统计学上的显著差异,但在同时考虑一揽子剂量学指数时,gMCO计划的通过率比IPSA高(高出1.3至1.6倍)。结论:与IPSA相比,gMCO的使用使前列腺HDR近距离治疗的计划时间缩短了一半,但不降低计划质量。与规划过程相关的总体效率提高导致我们在所有HDR前列腺病例中使用gMCO。
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引用次数: 0
Clinical outcomes with triple tandem brachytherapy for medically inoperable endometrial cancer in a high-risk patient population. 三次串联近距离放疗在高危人群中治疗医学上不能手术的子宫内膜癌的临床效果
IF 1.8 Pub Date : 2025-12-15 DOI: 10.1016/j.brachy.2025.10.010
Michael Jason Gutman, Tianming Wu, Aranee Sivananthan, Hania Al-Hallaq, Christina Son, Yasmin Hasan

Purpose: The purpose of this study is to evaluate clinical outcomes for medically inoperable endometrial cancer (MIEC) patients treated with triple tandem brachytherapy (TTB) ± external beam radiation therapy (EBRT).

Methods: This single institution retrospective review analyses MIEC patients treated definitively with TTB ± EBRT from 2014 to 2021. FIGO stage I-II with Grade 1-2 histology were considered low-risk endometrial cancer (LREC) and FIGO stage III-IVB and/or any Grade 3 endometrioid carcinoma, clear cell, or serous carcinoma were considered high-risk endometrial cancer (HREC). Planning parameters for target volume(s) and OARs (organs at risk) were per ABS guidelines. Overall survival (OS) and local failure-free survival (LFFS) were estimated by Kaplan-Meier analysis. Local control (LC), acute and late toxicities were evaluated clinically.

Results: Of 26 patients, 92.3% (n = 24) received TTB + EBRT. The median age at diagnosis was 66.5 years (40.5-88.7 years). Median follow up was 41.1 months (1.7-109.9 months). Median prescribed doses to the uterus were 45 Gy (0-50.4 Gy) for EBRT and 22.25 Gy (18-49.1 Gy) for TTB. 53.8% (n = 14) had LREC and 46.2% (n = 12) had HREC. 88.5% had endometrioid histology. The median OS for the entire cohort was 43.5 months with no difference for the LREC and HREC (p = 0.563). LC was superior (p = 0.032) in LREC patients (100% 4-year LFFS) with all recurrences occurring in the HREC cohort (1-/4-year LFFS 90.9%/62.3%). Late toxicities > Grade 2 were: Grade 2 GU (n = 2) and Grade 2 GI (n = 1).

Conclusions: Definitive TTB ± EBRT for MIEC patients was associated with excellent LFFS and acceptable toxicity rates.

目的:本研究的目的是评估医学上不能手术的子宫内膜癌(MIEC)患者接受三次串联近距离放疗(TTB)±外束放疗(EBRT)的临床效果。方法:本单机构回顾性分析2014年至2021年确定接受TTB±EBRT治疗的MIEC患者。FIGO I-II期和1-2级组织学被认为是低风险子宫内膜癌(LREC), FIGO III-IVB期和/或任何3级子宫内膜样癌、透明细胞癌或浆液性癌被认为是高风险子宫内膜癌(HREC)。目标体积(s)和OARs(危险器官)的规划参数按照ABS指南。通过Kaplan-Meier分析估计总生存期(OS)和局部无故障生存期(LFFS)。临床评价局部对照(LC)、急性和晚期毒性。结果:26例患者中,92.3% (n = 24)接受了TTB + EBRT治疗。诊断时的中位年龄为66.5岁(40.5-88.7岁)。中位随访时间为41.1个月(1.7 ~ 109.9个月)。EBRT给子宫的中位处方剂量为45 Gy(0-50.4 Gy), TTB为22.25 Gy(18-49.1 Gy)。53.8% (n = 14)为LREC, 46.2% (n = 12)为HREC。88.5%有子宫内膜样组织学。整个队列的中位生存期为43.5个月,LREC和HREC没有差异(p = 0.563)。LC在LREC患者(100% 4年LFFS)中更优越(p = 0.032),所有复发发生在HREC队列中(1-/4年LFFS 90.9%/62.3%)。晚期毒性> 2级为:2级GU (n = 2)和2级GI (n = 1)。结论:MIEC患者的明确TTB±EBRT与良好的LFFS和可接受的毒性率相关。
{"title":"Clinical outcomes with triple tandem brachytherapy for medically inoperable endometrial cancer in a high-risk patient population.","authors":"Michael Jason Gutman, Tianming Wu, Aranee Sivananthan, Hania Al-Hallaq, Christina Son, Yasmin Hasan","doi":"10.1016/j.brachy.2025.10.010","DOIUrl":"https://doi.org/10.1016/j.brachy.2025.10.010","url":null,"abstract":"<p><strong>Purpose: </strong>The purpose of this study is to evaluate clinical outcomes for medically inoperable endometrial cancer (MIEC) patients treated with triple tandem brachytherapy (TTB) ± external beam radiation therapy (EBRT).</p><p><strong>Methods: </strong>This single institution retrospective review analyses MIEC patients treated definitively with TTB ± EBRT from 2014 to 2021. FIGO stage I-II with Grade 1-2 histology were considered low-risk endometrial cancer (LREC) and FIGO stage III-IVB and/or any Grade 3 endometrioid carcinoma, clear cell, or serous carcinoma were considered high-risk endometrial cancer (HREC). Planning parameters for target volume(s) and OARs (organs at risk) were per ABS guidelines. Overall survival (OS) and local failure-free survival (LFFS) were estimated by Kaplan-Meier analysis. Local control (LC), acute and late toxicities were evaluated clinically.</p><p><strong>Results: </strong>Of 26 patients, 92.3% (n = 24) received TTB + EBRT. The median age at diagnosis was 66.5 years (40.5-88.7 years). Median follow up was 41.1 months (1.7-109.9 months). Median prescribed doses to the uterus were 45 Gy (0-50.4 Gy) for EBRT and 22.25 Gy (18-49.1 Gy) for TTB. 53.8% (n = 14) had LREC and 46.2% (n = 12) had HREC. 88.5% had endometrioid histology. The median OS for the entire cohort was 43.5 months with no difference for the LREC and HREC (p = 0.563). LC was superior (p = 0.032) in LREC patients (100% 4-year LFFS) with all recurrences occurring in the HREC cohort (1-/4-year LFFS 90.9%/62.3%). Late toxicities > Grade 2 were: Grade 2 GU (n = 2) and Grade 2 GI (n = 1).</p><p><strong>Conclusions: </strong>Definitive TTB ± EBRT for MIEC patients was associated with excellent LFFS and acceptable toxicity rates.</p>","PeriodicalId":93914,"journal":{"name":"Brachytherapy","volume":" ","pages":""},"PeriodicalIF":1.8,"publicationDate":"2025-12-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145770296","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Rectal spacers in high-dose-rate-brachytherapy: Optimizing peripheral zone radiation delivery. 直肠间隔器在高剂量率近距离放疗中的应用:优化外周区放射输送。
IF 1.8 Pub Date : 2025-12-13 DOI: 10.1016/j.brachy.2025.10.014
Christopher A Cronkite, David Lakomy, Arjit Baghwala, Ramiro Pino, Andrew M Farach
<p><strong>Background: </strong>The utilization of rectal spacers (RS) in prostate cancer treated with definitive radiotherapy has been shown to provide rectal dose sparing, decreased rectal toxicity, and improved gastrointestinal quality-of-life metrics. This dose-sparing effect presents an opportunity for dose escalation to the prostate, potentially enhancing clinical and biochemical outcomes while minimizing adverse effects. Although the influence of RS on overall prostate dosimetry has yielded mixed findings, the specific impact on radiation delivery to the predominantly tumorigenic peripheral zone (PZ) remains largely unexamined. This study aims to evaluate the effects of RS on PZ dosimetry in prostate brachytherapy.</p><p><strong>Methods: </strong>A single-institution, retrospective analysis was conducted on patients who received two-fraction high-dose-rate brachytherapy (HDR-BT) for localized prostate cancer. Dosimetric parameters and biochemical outcomes were compared between consecutive patients who received intraoperative RS (RS+) and those who did not (RS-). Additional subset analysis was performed stratifying by prostate size. Comparisons were performed using the Mann-Whitney U test. Dosimetric parameters were assessed for the prostate, planning target volume, PZ, and organs at risk (OAR).</p><p><strong>Results: </strong>Between January 2020 and July 2024, a total of 92 patients who underwent HDR-BT were identified, of whom 46 (50%) were RS+. The contoured volumes of the prostate and PZ were comparable between the RS- and RS+ cohorts, with a median of 38.5 vs. 34.96 cm<sup>3</sup> (p = 0.4475) and 11.25 vs. 10.25 (p = 0.1964), respectively, for the prostate and PZ. However, median PZ D<sub>90</sub> was significantly higher in RS+ patients compared to RS- (RZ+ 115.65% vs. 110.25%, p < 0.0001). The increase in PZ D<sub>90</sub> in the RS+ group was more pronounced in patients with smaller prostates (<40 cm<sup>3</sup>: RS+ 115.97% vs. 108.87%, p < 0.0001). Regarding organs at risk, the RS+ group exhibited a reduction in rectal D<sub>max</sub> (p < 0.0001), V<sub>20</sub> (p = 0.0002), D<sub>80</sub> (p < 0.0001), and D<sub>2cc</sub> (p < 0.0001); a decrease in urethral D<sub>max</sub> (p = 0.0017) and V<sub>110</sub> (p = 0.0002); and an increase in bladder V<sub>75</sub> and D<sub>80</sub> (p < 0.0001).</p><p><strong>Conclusions: </strong>As expected, RS HDR-BT successfully reduced rectal radiation exposure in this cohort. RS use is associated with increased radiation delivery to the PZ, potentially augmenting ablative dosing to the primary site of disease and the most likely zone for potential microscopic intraprostatic spread, as well as decreased urethral doses. This enhanced dose distribution within the PZ, with simultaneous improved urethral sparing, supports the incorporation of RS in HDR-BT. Whether this dosimetric enhancement results in long-term biochemical control or improved overall oncologic outcomes remains an ongoing area
背景:直肠间隔剂(RS)在前列腺癌放射治疗中的应用已被证明可以节省直肠剂量,降低直肠毒性,并改善胃肠道生活质量指标。这种剂量节约效应为前列腺剂量增加提供了机会,潜在地增强临床和生化结果,同时最大限度地减少不良反应。虽然RS对总体前列腺剂量学的影响产生了不同的结果,但对主要致瘤性外周区(PZ)辐射传递的具体影响在很大程度上仍未得到研究。本研究旨在探讨RS对前列腺近距离放射治疗中PZ剂量学的影响。方法:采用单机构回顾性分析,对接受两段式高剂量率近距离放疗(HDR-BT)治疗局限性前列腺癌的患者进行分析。比较连续接受术中RS (RS+)和未接受RS (RS-)的患者的剂量学参数和生化结果。根据前列腺大小进行额外的亚群分析。采用Mann-Whitney U检验进行比较。评估了前列腺、计划靶体积、PZ和危险器官(OAR)的剂量学参数。结果:2020年1月至2024年7月,共发现92例HDR-BT患者,其中46例(50%)为RS+。前列腺和PZ的轮廓体积在RS-和RS+队列之间具有可比性,前列腺和PZ的中位数分别为38.5和34.96 cm3 (p = 0.4475)和11.25和10.25 (p = 0.1964)。然而,平均PZ D90明显高于在RS +患者相比,RS - (RZ + 115.65%比110.25%,p RS +组有90人在较小的前列腺患者更明显(3:RS + 115.97%比108.87%,p max (p 20 (p = 0.0002),D80 (p 2 cc (p max (p = 0.0017)和V110 (p = 0.0002);结论:正如预期的那样,RS HDR-BT在该队列中成功地减少了直肠辐射暴露。RS的使用与PZ的放射量增加有关,潜在地增加了疾病原发部位的消融剂量和潜在的显微前列腺内扩散最有可能的区域,以及尿道剂量的减少。PZ内的剂量分布增强,同时改善尿道保留,支持RS在HDR-BT中的结合。这种剂量增强是否会导致长期生化控制或改善总体肿瘤预后,仍是一个正在进行的研究领域。
{"title":"Rectal spacers in high-dose-rate-brachytherapy: Optimizing peripheral zone radiation delivery.","authors":"Christopher A Cronkite, David Lakomy, Arjit Baghwala, Ramiro Pino, Andrew M Farach","doi":"10.1016/j.brachy.2025.10.014","DOIUrl":"https://doi.org/10.1016/j.brachy.2025.10.014","url":null,"abstract":"&lt;p&gt;&lt;strong&gt;Background: &lt;/strong&gt;The utilization of rectal spacers (RS) in prostate cancer treated with definitive radiotherapy has been shown to provide rectal dose sparing, decreased rectal toxicity, and improved gastrointestinal quality-of-life metrics. This dose-sparing effect presents an opportunity for dose escalation to the prostate, potentially enhancing clinical and biochemical outcomes while minimizing adverse effects. Although the influence of RS on overall prostate dosimetry has yielded mixed findings, the specific impact on radiation delivery to the predominantly tumorigenic peripheral zone (PZ) remains largely unexamined. This study aims to evaluate the effects of RS on PZ dosimetry in prostate brachytherapy.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Methods: &lt;/strong&gt;A single-institution, retrospective analysis was conducted on patients who received two-fraction high-dose-rate brachytherapy (HDR-BT) for localized prostate cancer. Dosimetric parameters and biochemical outcomes were compared between consecutive patients who received intraoperative RS (RS+) and those who did not (RS-). Additional subset analysis was performed stratifying by prostate size. Comparisons were performed using the Mann-Whitney U test. Dosimetric parameters were assessed for the prostate, planning target volume, PZ, and organs at risk (OAR).&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Results: &lt;/strong&gt;Between January 2020 and July 2024, a total of 92 patients who underwent HDR-BT were identified, of whom 46 (50%) were RS+. The contoured volumes of the prostate and PZ were comparable between the RS- and RS+ cohorts, with a median of 38.5 vs. 34.96 cm&lt;sup&gt;3&lt;/sup&gt; (p = 0.4475) and 11.25 vs. 10.25 (p = 0.1964), respectively, for the prostate and PZ. However, median PZ D&lt;sub&gt;90&lt;/sub&gt; was significantly higher in RS+ patients compared to RS- (RZ+ 115.65% vs. 110.25%, p &lt; 0.0001). The increase in PZ D&lt;sub&gt;90&lt;/sub&gt; in the RS+ group was more pronounced in patients with smaller prostates (&lt;40 cm&lt;sup&gt;3&lt;/sup&gt;: RS+ 115.97% vs. 108.87%, p &lt; 0.0001). Regarding organs at risk, the RS+ group exhibited a reduction in rectal D&lt;sub&gt;max&lt;/sub&gt; (p &lt; 0.0001), V&lt;sub&gt;20&lt;/sub&gt; (p = 0.0002), D&lt;sub&gt;80&lt;/sub&gt; (p &lt; 0.0001), and D&lt;sub&gt;2cc&lt;/sub&gt; (p &lt; 0.0001); a decrease in urethral D&lt;sub&gt;max&lt;/sub&gt; (p = 0.0017) and V&lt;sub&gt;110&lt;/sub&gt; (p = 0.0002); and an increase in bladder V&lt;sub&gt;75&lt;/sub&gt; and D&lt;sub&gt;80&lt;/sub&gt; (p &lt; 0.0001).&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Conclusions: &lt;/strong&gt;As expected, RS HDR-BT successfully reduced rectal radiation exposure in this cohort. RS use is associated with increased radiation delivery to the PZ, potentially augmenting ablative dosing to the primary site of disease and the most likely zone for potential microscopic intraprostatic spread, as well as decreased urethral doses. This enhanced dose distribution within the PZ, with simultaneous improved urethral sparing, supports the incorporation of RS in HDR-BT. Whether this dosimetric enhancement results in long-term biochemical control or improved overall oncologic outcomes remains an ongoing area","PeriodicalId":93914,"journal":{"name":"Brachytherapy","volume":" ","pages":""},"PeriodicalIF":1.8,"publicationDate":"2025-12-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145758696","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Association between rectal spacer use and bowel, urinary, and sexual dysfunction following prostate cancer brachytherapy: U.S. claims data analysis. 前列腺癌近距离治疗后直肠垫片使用与肠、尿、性功能障碍的关系:美国索赔数据分析
IF 1.8 Pub Date : 2025-12-13 DOI: 10.1016/j.brachy.2025.10.015
Michael R Folkert, Emily S Weg, Ryoko Sato, James B Yu, Samir Bhattacharyya, Emmanuel Ezekekwu, Daniel A Hamstra

Purpose: Rectal spacing has been shown to reduce toxicity following external beam radiation therapy for prostate cancer. However, real-world evidence of effectiveness for rectal spacers with brachytherapy (BT) monotherapy remains limited. This study used U.S. claims datasets to assess the association between rectal spacer use and bowel, urinary, and sexual function following BT.

Materials and methods: A retrospective study was conducted among patients treated with BT monotherapy for prostate cancer between 2015 and 2021, using Medicare 5% and 100% Files, MarketScan, and Premier Databases. Polyethylene glycol rectal spacer use was identified. Post-BT treatment diagnoses of bowel, urinary, and sexual dysfunction were evaluated using Cox proportional hazards models, adjusting for age, comorbidity, region, baseline dysfunction, secondary cancers, and BT modality (low-dose rate [LDR] or high-dose rate).

Results: Among 13,858 BT monotherapy patients, 1198 (8.6%) received a spacer. Patients with spacer were younger and had fewer baseline dysfunctions. At 5-year median follow-up, spacer use was associated with significantly lower incidence of bowel (adjusted hazard ratio, aHR: 0.76, p = 0.027) and urinary (aHR: 0.84, p = 0.008) dysfunction. Sexual dysfunction trended lower (aHR: 0.79, p = 0.120), although not significant. In LDR patients, spacer use remained significantly associated with reduced bowel (aHR: 0.74, p = 0.021) and urinary (aHR: 0.83, p = 0.005) dysfunction. Significant associations were not found in high-dose rate patients.

Conclusions: In this large real-world study, rectal spacing as a standard-of-care intervention showed sustained significant benefit in reducing bowel and urinary dysfunction, which appeared to be greatest in those treated with LDR BT.

目的:直肠间距已被证明可以减少前列腺癌体外放射治疗后的毒性。然而,实际证据表明直肠间隔剂与近距离治疗(BT)单一疗法的有效性仍然有限。本研究使用美国索赔数据集来评估直肠间隔剂使用与BT治疗后肠、尿和性功能之间的关系。材料和方法:在2015年至2021年间接受BT单药治疗的前列腺癌患者中进行了一项回顾性研究,使用了Medicare 5%和100% Files、MarketScan和Premier数据库。确定了聚乙二醇直肠垫片的使用。使用Cox比例风险模型,调整年龄、合并症、地区、基线功能障碍、继发癌症和BT方式(低剂量率[LDR]或高剂量率),评估BT治疗后肠、尿和性功能障碍的诊断。结果:13858例BT单药治疗患者中,1198例(8.6%)接受间隔剂治疗。使用间隔剂的患者更年轻,基线功能障碍更少。在中位5年随访中,间隔器的使用与肠道功能障碍(校正风险比,aHR: 0.76, p = 0.027)和泌尿功能障碍(aHR: 0.84, p = 0.008)的发生率显著降低相关。性功能障碍倾向较低(aHR: 0.79, p = 0.120),但不显著。在LDR患者中,间隔器的使用与肠道功能障碍的减少(aHR: 0.74, p = 0.021)和泌尿功能障碍(aHR: 0.83, p = 0.005)仍然显著相关。在高剂量率患者中未发现显著相关性。结论:在这项大型现实世界的研究中,直肠间距作为一种标准护理干预措施,在减少肠道和泌尿功能障碍方面显示出持续的显著益处,这在接受LDR BT治疗的患者中似乎是最大的。
{"title":"Association between rectal spacer use and bowel, urinary, and sexual dysfunction following prostate cancer brachytherapy: U.S. claims data analysis.","authors":"Michael R Folkert, Emily S Weg, Ryoko Sato, James B Yu, Samir Bhattacharyya, Emmanuel Ezekekwu, Daniel A Hamstra","doi":"10.1016/j.brachy.2025.10.015","DOIUrl":"https://doi.org/10.1016/j.brachy.2025.10.015","url":null,"abstract":"<p><strong>Purpose: </strong>Rectal spacing has been shown to reduce toxicity following external beam radiation therapy for prostate cancer. However, real-world evidence of effectiveness for rectal spacers with brachytherapy (BT) monotherapy remains limited. This study used U.S. claims datasets to assess the association between rectal spacer use and bowel, urinary, and sexual function following BT.</p><p><strong>Materials and methods: </strong>A retrospective study was conducted among patients treated with BT monotherapy for prostate cancer between 2015 and 2021, using Medicare 5% and 100% Files, MarketScan, and Premier Databases. Polyethylene glycol rectal spacer use was identified. Post-BT treatment diagnoses of bowel, urinary, and sexual dysfunction were evaluated using Cox proportional hazards models, adjusting for age, comorbidity, region, baseline dysfunction, secondary cancers, and BT modality (low-dose rate [LDR] or high-dose rate).</p><p><strong>Results: </strong>Among 13,858 BT monotherapy patients, 1198 (8.6%) received a spacer. Patients with spacer were younger and had fewer baseline dysfunctions. At 5-year median follow-up, spacer use was associated with significantly lower incidence of bowel (adjusted hazard ratio, aHR: 0.76, p = 0.027) and urinary (aHR: 0.84, p = 0.008) dysfunction. Sexual dysfunction trended lower (aHR: 0.79, p = 0.120), although not significant. In LDR patients, spacer use remained significantly associated with reduced bowel (aHR: 0.74, p = 0.021) and urinary (aHR: 0.83, p = 0.005) dysfunction. Significant associations were not found in high-dose rate patients.</p><p><strong>Conclusions: </strong>In this large real-world study, rectal spacing as a standard-of-care intervention showed sustained significant benefit in reducing bowel and urinary dysfunction, which appeared to be greatest in those treated with LDR BT.</p>","PeriodicalId":93914,"journal":{"name":"Brachytherapy","volume":" ","pages":""},"PeriodicalIF":1.8,"publicationDate":"2025-12-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145758706","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Multicatheter interstitial brachytherapy-delivered APBI as single-fraction treatment in older breast cancer patients: A feasibility retrospective institutional analysis. 多导管间质近距离APBI作为单组分治疗老年乳腺癌患者:可行性回顾性机构分析。
IF 1.8 Pub Date : 2025-12-11 DOI: 10.1016/j.brachy.2025.11.002
Catarina van der Elzen, Diana Correia, Sofia Garcia, Pedro Fernandes, Alexandre Pereira, Sara Pinto, Marina Maçães, Inês Lima, Lurdes Trigo

Purpose: Accelerated partial breast irradiation (APBI) has emerged as an alternative to whole-breast irradiation (WBI) for selected patients with low-risk early breast cancer (EBC). While external beam APBI techniques are widely available, multicatheter interstitial brachytherapy (MIB) offers superior conformity and reduced normal tissue exposure. We evaluated the feasibility, toxicity, and early outcomes of an ultra-hypo fractionated approach using a single-fraction MIB-APBI in older patients.

Methods and materials: We conducted a single-institution retrospective study of 20 women (range, 69-88 years) with low-risk EBC treated with a single-fraction APBI (uAPBI) 16 Gy using MIB, between January 2023 and October 2024. All patients had undergone lumpectomy with sentinel lymph node biopsy. Eligibility criteria included age ≥65 years, tumor size ≤3 cm, unifocal disease, sentinel node-negative status and microscopically clear resection margins. Acute and late toxicities, cosmetic outcomes, oncological endpoints and dosimetric parameters were evaluated.

Results: Acute toxicity was limited to Grade 1/2 dermatitis in 25% of patients while no severe late toxicity was observed. Cosmetic outcomes were excellent to good in 100% of patients. At median follow-up of 18 months (range, 10-26), all patients remained alive with no locoregional recurrence or distant metastasis. Dosimetric parameters demonstrated excellent target coverage (median V100%: 97%, range 90-98%).

Conclusions: Single-fraction MIB-based APBI delivering 16 Gy appears to be a feasible, well-tolerated, and effective treatment approach for carefully selected older patients with EBC. This ultra-hypo fractionated approach significantly reduces treatment burden while maintaining excellent local control and favorable toxicity profiles.

目的:加速部分乳房照射(APBI)已成为低风险早期乳腺癌(EBC)患者全乳房照射(WBI)的替代方案。虽然外束APBI技术广泛可用,但多导管间质近距离治疗(MIB)提供了优越的一致性和减少正常组织暴露。我们评估了在老年患者中使用单组分mb - apbi的超低分级方法的可行性、毒性和早期结果。方法和材料:我们在2023年1月至2024年10月期间,对20名低风险EBC患者(范围,69-88岁)进行了单机构回顾性研究,使用MIB进行了单组分APBI (uAPBI) 16 Gy治疗。所有患者均行乳房肿瘤切除术及前哨淋巴结活检。入选标准包括年龄≥65岁,肿瘤大小≤3 cm,单灶性疾病,前哨淋巴结阴性,镜下切除边缘清晰。评估急性和晚期毒性、美容结果、肿瘤终点和剂量学参数。结果:25%的患者急性毒性仅限于1/2级皮炎,未观察到严重的晚期毒性。100%的患者的美容效果都很好。中位随访18个月(范围10-26个月),所有患者均存活,无局部复发或远处转移。剂量学参数显示极好的靶覆盖率(中位数V100%: 97%,范围90-98%)。结论:对于精心挑选的老年EBC患者,基于单组分mb的APBI给药16 Gy似乎是一种可行、耐受性良好且有效的治疗方法。这种超低分级方法显著减少了治疗负担,同时保持了良好的局部控制和有利的毒性特征。
{"title":"Multicatheter interstitial brachytherapy-delivered APBI as single-fraction treatment in older breast cancer patients: A feasibility retrospective institutional analysis.","authors":"Catarina van der Elzen, Diana Correia, Sofia Garcia, Pedro Fernandes, Alexandre Pereira, Sara Pinto, Marina Maçães, Inês Lima, Lurdes Trigo","doi":"10.1016/j.brachy.2025.11.002","DOIUrl":"https://doi.org/10.1016/j.brachy.2025.11.002","url":null,"abstract":"<p><strong>Purpose: </strong>Accelerated partial breast irradiation (APBI) has emerged as an alternative to whole-breast irradiation (WBI) for selected patients with low-risk early breast cancer (EBC). While external beam APBI techniques are widely available, multicatheter interstitial brachytherapy (MIB) offers superior conformity and reduced normal tissue exposure. We evaluated the feasibility, toxicity, and early outcomes of an ultra-hypo fractionated approach using a single-fraction MIB-APBI in older patients.</p><p><strong>Methods and materials: </strong>We conducted a single-institution retrospective study of 20 women (range, 69-88 years) with low-risk EBC treated with a single-fraction APBI (uAPBI) 16 Gy using MIB, between January 2023 and October 2024. All patients had undergone lumpectomy with sentinel lymph node biopsy. Eligibility criteria included age ≥65 years, tumor size ≤3 cm, unifocal disease, sentinel node-negative status and microscopically clear resection margins. Acute and late toxicities, cosmetic outcomes, oncological endpoints and dosimetric parameters were evaluated.</p><p><strong>Results: </strong>Acute toxicity was limited to Grade 1/2 dermatitis in 25% of patients while no severe late toxicity was observed. Cosmetic outcomes were excellent to good in 100% of patients. At median follow-up of 18 months (range, 10-26), all patients remained alive with no locoregional recurrence or distant metastasis. Dosimetric parameters demonstrated excellent target coverage (median V100%: 97%, range 90-98%).</p><p><strong>Conclusions: </strong>Single-fraction MIB-based APBI delivering 16 Gy appears to be a feasible, well-tolerated, and effective treatment approach for carefully selected older patients with EBC. This ultra-hypo fractionated approach significantly reduces treatment burden while maintaining excellent local control and favorable toxicity profiles.</p>","PeriodicalId":93914,"journal":{"name":"Brachytherapy","volume":" ","pages":""},"PeriodicalIF":1.8,"publicationDate":"2025-12-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145746116","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
A mediation analysis of laboratory indicators affecting seed migration after 125I brachytherapy in hepatic malignancies. 肝恶性肿瘤125I近距离放射治疗后影响种子迁移的实验室指标的中介分析。
IF 1.8 Pub Date : 2025-12-10 DOI: 10.1016/j.brachy.2025.10.016
Junfeng Lin, Ang Li, Jianqiang Ye, Zewen Han, Lili Lin, Han Jiang, Junqing Lin

Background: 125I seed migration is a persistent safety concern in hepatic brachytherapy. Inflammatory and metabolic biomarkers may influence both tissue vulnerability and implantation strategies, contributing to migration risk.

Methods: In this retrospective study of 625 patients undergoing 125I seed implantation for primary or metastatic liver tumors, clinical, laboratory, and procedural data were analyzed. Migration was assessed via follow-up chest radiography or CT. Univariate and multivariate Cox regression identified predictors of migration. Kaplan-Meier analysis evaluated seed migration-free survival (SMFS). Causal mediation analysis examined whether procedural factors-total number of seeds implanted (NSI) and maximum number per session (MAX)-mediated the effects of lactate dehydrogenase (LDH), neutrophil ratio, and lymphocyte ratio on migration.

Results: Seed migration occurred in 134 patients (21.4%). Elevated LDH, neutrophil ratio, MAX, and NSI were significantly associated with migration (all p < 0.01), while higher lymphocyte ratio was protective. Cox regression identified LDH, MAX, lymphocyte ratio, platelet count, and NSI as independent predictors. Kaplan-Meier analysis showed shorter SMFS in patients with high LDH or neutrophils and low lymphocytes. Mediation analysis revealed that LDH and neutrophils increased migration risk both directly and indirectly through procedural intensity (MAX, NSI), whereas lymphocytes had protective effects via both pathways.

Conclusion: Systemic inflammation and metabolic status influence both physiologic susceptibility and procedural factors associated with 125I seed migration. Causal mediation analysis highlights modifiable indirect mechanisms, supporting personalized implantation planning to reduce migration risk.

背景:125I粒子迁移是肝脏近距离放射治疗中一个持续存在的安全性问题。炎症和代谢生物标志物可能影响组织易损性和植入策略,从而增加迁移风险。方法:回顾性分析625例原发性或转移性肝肿瘤行125I粒子植入术的患者的临床、实验室和手术资料。通过随访胸片或CT评估迁移。单因素和多因素Cox回归确定了迁移的预测因素。Kaplan-Meier分析评估种子无迁移存活率(SMFS)。因果中介分析考察了程序性因素——植入种子总数(NSI)和每节最大种子数(MAX)——是否介导了乳酸脱氢酶(LDH)、中性粒细胞比例和淋巴细胞比例对迁移的影响。结果:134例(21.4%)患者发生种子迁移。LDH、中性粒细胞比例、MAX和NSI升高与125I种子迁移显著相关(均p )结论:全身性炎症和代谢状态影响与125I种子迁移相关的生理易感性和程序性因素。因果中介分析强调可修改的间接机制,支持个性化的植入计划以减少迁移风险。
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Brachytherapy
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