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.
{"title":"Caudally directed posterior high-dose-rate brachytherapy for reirradiation of para-aortic lymph node recurrence: A technical innovation enabled by interventional radiology.","authors":"Kae Okuma, Yasuaki Arai, Mizuki Ozawa, Hiroki Nakayama, Hiroyuki Okamoto, Ayaka Nagao, Koji Inaba, Tairo Kashihara, Kana Takahashi, Madoka Sakuramachi, Akane Yoshiba, Hiroshi Igaki","doi":"10.1016/j.brachy.2025.11.008","DOIUrl":"https://doi.org/10.1016/j.brachy.2025.11.008","url":null,"abstract":"<p><strong>Purpose: </strong>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.</p><p><strong>Methods and materials: </strong>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.</p><p><strong>Results: </strong>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.</p><p><strong>Conclusions: </strong>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.</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":"145776807","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}
Pub Date : 2025-12-16DOI: 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.
{"title":"Evaluation of AI chatbot responses to brachytherapy frequently asked questions.","authors":"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","doi":"10.1016/j.brachy.2025.10.005","DOIUrl":"https://doi.org/10.1016/j.brachy.2025.10.005","url":null,"abstract":"<p><strong>Purpose: </strong>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.</p><p><strong>Methods: </strong>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.</p><p><strong>Results: </strong>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.</p><p><strong>Conclusions: </strong>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.</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":"145776770","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}
Pub Date : 2025-12-16DOI: 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.
{"title":"Low dose iodine-125 brachytherapy and transpupillary thermal therapy for small- to medium-sized choroidal melanoma.","authors":"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","doi":"10.1016/j.brachy.2025.11.011","DOIUrl":"https://doi.org/10.1016/j.brachy.2025.11.011","url":null,"abstract":"<p><strong>Purpose: </strong>COMS established iodine-125 (<sup>125</sup>I) 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 <sup>125</sup>I brachytherapy on local tumor control and ocular adverse events (AEs).</p><p><strong>Methods: </strong>Patients diagnosed 2005-2019 with choroidal melanoma <5 mm thick and managed with <sup>125</sup>I 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.</p><p><strong>Results: </strong>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%.</p><p><strong>Conclusion: </strong>Reduced dose <sup>125</sup>I brachytherapy is feasible with excellent local tumor control.</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":"145776834","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}
Pub Date : 2025-12-16DOI: 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.
{"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}
Pub Date : 2025-12-15DOI: 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.
{"title":"A first-in-human randomized clinical trial of graphics processing units based multi-criteria optimization (gMCO) versus IPSA in high-dose-rate prostate brachytherapy.","authors":"F Lacroix, E Poulin, C Bélanger, S Aubin, D Carignan, E Vigneault, A-G Martin, F Bachand, L Beaulieu, W Foster","doi":"10.1016/j.brachy.2025.11.009","DOIUrl":"https://doi.org/10.1016/j.brachy.2025.11.009","url":null,"abstract":"<p><strong>Purpose: </strong>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.</p><p><strong>Methods and materials: </strong>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.</p><p><strong>Results: </strong>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.</p><p><strong>Conclusion: </strong>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.</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":"145770260","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}
Pub Date : 2025-12-15DOI: 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.
{"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}
Pub Date : 2025-12-13DOI: 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
{"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":"<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","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}
Pub Date : 2025-12-13DOI: 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}
Pub Date : 2025-12-11DOI: 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.
{"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}
Pub Date : 2025-12-10DOI: 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.
{"title":"A mediation analysis of laboratory indicators affecting seed migration after <sup>125</sup>I brachytherapy in hepatic malignancies.","authors":"Junfeng Lin, Ang Li, Jianqiang Ye, Zewen Han, Lili Lin, Han Jiang, Junqing Lin","doi":"10.1016/j.brachy.2025.10.016","DOIUrl":"https://doi.org/10.1016/j.brachy.2025.10.016","url":null,"abstract":"<p><strong>Background: </strong><sup>125</sup>I 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.</p><p><strong>Methods: </strong>In this retrospective study of 625 patients undergoing <sup>125</sup>I 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.</p><p><strong>Results: </strong>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.</p><p><strong>Conclusion: </strong>Systemic inflammation and metabolic status influence both physiologic susceptibility and procedural factors associated with <sup>125</sup>I seed migration. Causal mediation analysis highlights modifiable indirect mechanisms, supporting personalized implantation planning to reduce migration risk.</p>","PeriodicalId":93914,"journal":{"name":"Brachytherapy","volume":" ","pages":""},"PeriodicalIF":1.8,"publicationDate":"2025-12-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145746074","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}