首页 > 最新文献

Brachytherapy最新文献

英文 中文
Ultrasound and CT-guided implantation of iodine-125 seeds combined with transarterial chemoembolization for recurrent hepatocellular carcinoma at complex sites after hepatectomy
IF 1.7 4区 医学 Q4 ONCOLOGY Pub Date : 2025-03-01 DOI: 10.1016/j.brachy.2024.12.002
Yeyan Wang , Jie Feng

OBJECTIVE

The objective of this study was to evaluate the efficacy and safety of TACE combined with 125I seeds (TACE-125I) in the treatment of recurrent HCC at complex sites after hepatectomy.

METHODS

This study retrospectively analyzed the clinical data of recurrent HCC patients located at complex sites (such as large blood vessels, diaphragm dome, etc.) after hepatectomy from January 2012 to December 2023, all of whom received TACE-125I or TACE therapy. Recur rence, overall survival (OS), progression-free survival (PFS) and complications were compared be tween the 2 groups.

RESULTS

A total of 152 patients with recurrent HCC were enrolled in this study, including 69 in the TACE-125I group and 83 in the TACE group. During follow-up, a total of 41 patients in the TACE-125I group experienced tumor recurrence, compared to 67 patients in the TACE group. The median OS in the TACE-125I group was 31 months, which was significantly higher than that in the TACE group (16 months, p < 0.001). Similarly, the median PFS was significantly higher in the TACE-125I group than in the TACE group.

CONCLUSIONS

Compared with TACE treatment, TACE-125I may be a more effective method for the treatment of recurrent HCC located at complex sites.
{"title":"Ultrasound and CT-guided implantation of iodine-125 seeds combined with transarterial chemoembolization for recurrent hepatocellular carcinoma at complex sites after hepatectomy","authors":"Yeyan Wang ,&nbsp;Jie Feng","doi":"10.1016/j.brachy.2024.12.002","DOIUrl":"10.1016/j.brachy.2024.12.002","url":null,"abstract":"<div><h3>OBJECTIVE</h3><div>The objective of this study was to evaluate the efficacy and safety of TACE combined with 125I seeds (TACE-125I) in the treatment of recurrent HCC at complex sites after hepatectomy.</div></div><div><h3>METHODS</h3><div>This study retrospectively analyzed the clinical data of recurrent HCC patients located at complex sites (such as large blood vessels, diaphragm dome, etc.) after hepatectomy from January 2012 to December 2023, all of whom received TACE-125I or TACE therapy. Recur rence, overall survival (OS), progression-free survival (PFS) and complications were compared be tween the 2 groups.</div></div><div><h3>RESULTS</h3><div>A total of 152 patients with recurrent HCC were enrolled in this study, including 69 in the TACE-125I group and 83 in the TACE group. During follow-up, a total of 41 patients in the TACE-125I group experienced tumor recurrence, compared to 67 patients in the TACE group. The median OS in the TACE-125I group was 31 months, which was significantly higher than that in the TACE group (16 months, <em>p</em> &lt; 0.001). Similarly, the median PFS was significantly higher in the TACE-125I group than in the TACE group.</div></div><div><h3>CONCLUSIONS</h3><div>Compared with TACE treatment, TACE-125I may be a more effective method for the treatment of recurrent HCC located at complex sites.</div></div>","PeriodicalId":55334,"journal":{"name":"Brachytherapy","volume":"24 2","pages":"Pages 293-300"},"PeriodicalIF":1.7,"publicationDate":"2025-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143043970","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Learning curve and proficiency assessment for gynecological brachytherapy amongst radiation oncology trainees in India: Results from a prospective study 印度放射肿瘤学受训人员妇科近距离放疗的学习曲线和熟练程度评估:一项前瞻性研究的结果。
IF 1.7 4区 医学 Q4 ONCOLOGY Pub Date : 2025-03-01 DOI: 10.1016/j.brachy.2024.11.013
Bharath Kumar , Prachi Mittal , Ankita Gupta , Jaahid Mulani , Rajesh Bhajbhuje , Sadhana Kannan , Jeevanshu Jain , Supriya Chopra

PURPOSE

The quality of cervical cancer intracavitary brachytherapy (ICBT) depends on the training and experience of the radiation oncologist (RO). The present study was performed to establish primary learning curve for ICBT.

MATERIALS AND METHODS

Forty-three skill parameters were identified for performing ICBT and were included for Brachytherapy Proficiency Assessment and Scoring System (Brachy-PASS) questionnaire. Brachy-PASS score was first compared with blinded objective scoring of implant quality for 10 trainees by two ROs. Twenty eight consecutive trainees were scored with Brachy-PASS by two RO's. The impact of number of procedures and training years was ascertained using Mann Whitney-U test. Minimum number of intracavitary procedures to attain proficiency (score 75%) were ascertained and learning curve plot of proficiency and procedures was generated.

RESULTS

Between January, 2022 to September, 2023 38 trainees were evaluated (20: post graduate year (PGY) 1-3, and 18: PGY 4-5) after due consent for skill evaluation. Good congruence was reported of objective scoring and Brachy-PASS (83.4% vs 88%). Ten trainees had performed <15 ICBT, and 28 had performed ≥15 ICBT procedures. Overall 30/38 trainees (78.9%) achieved a Brachy-PASS score of ≥129 (75%). The average score for trainees with <15 procedures was 126.6 (73.6%) vs 148.8 (86.5%) in trainees who performed ≥15 procedures. PGY 4-5 trainees had higher score (153.8 (89.4%) vs 134 (77.9%)). Learning curve threshold of 15 ICBT was identified to attain 75% score (129/172) with no plateauing of learning curve even with 30 procedures.

CONCLUSION

Competency is established for independently performing intracavitary brachytherapy at 15 procedures and further increase in competency scores continues with increasing procedures.
目的:宫颈癌腔内近距离放疗(ICBT)的质量取决于放射肿瘤学家(RO)的培训和经验。本研究旨在建立ICBT的初步学习曲线。材料与方法:选取43项进行ICBT的技能参数,并将其纳入近距离治疗水平评估与评分系统(Brachy-PASS)问卷。首先将Brachy-PASS评分与2个ROs对10名受术者种植体质量的盲法客观评分进行比较。连续28名学员被2名RO评分为Brachy-PASS。采用Mann Whitney-U检验确定手术次数和训练年限的影响。确定达到熟练程度的最小腔内手术次数(评分≥75%),并生成熟练程度和手术的学习曲线图。结果:在2022年1月至2023年9月期间,对38名学员进行了技能评估,其中20名:研究生1-3年级,18名:研究生4-5年级。客观评分与Brachy-PASS的一致性较好(83.4% vs 88%)。结论:独立进行腔内近距离放射治疗15次的能力已经建立,能力得分随着手术次数的增加而进一步提高。
{"title":"Learning curve and proficiency assessment for gynecological brachytherapy amongst radiation oncology trainees in India: Results from a prospective study","authors":"Bharath Kumar ,&nbsp;Prachi Mittal ,&nbsp;Ankita Gupta ,&nbsp;Jaahid Mulani ,&nbsp;Rajesh Bhajbhuje ,&nbsp;Sadhana Kannan ,&nbsp;Jeevanshu Jain ,&nbsp;Supriya Chopra","doi":"10.1016/j.brachy.2024.11.013","DOIUrl":"10.1016/j.brachy.2024.11.013","url":null,"abstract":"<div><h3>PURPOSE</h3><div>The quality of cervical cancer intracavitary brachytherapy (ICBT) depends on the training and experience of the radiation oncologist (RO). The present study was performed to establish primary learning curve for ICBT.</div></div><div><h3>MATERIALS AND METHODS</h3><div>Forty-three skill parameters were identified for performing ICBT and were included for Brachytherapy Proficiency Assessment and Scoring System (Brachy-PASS) questionnaire. Brachy-PASS score was first compared with blinded objective scoring of implant quality for 10 trainees by two ROs. Twenty eight consecutive trainees were scored with Brachy-PASS by two RO's. The impact of number of procedures and training years was ascertained using Mann Whitney-U test. Minimum number of intracavitary procedures to attain proficiency (score<span><math><mo>≥</mo></math></span> 75%) were ascertained and learning curve plot of proficiency and procedures was generated.</div></div><div><h3>RESULTS</h3><div>Between January, 2022 to September, 2023 38 trainees were evaluated (20: post graduate year (PGY) 1-3, and 18: PGY 4-5) after due consent for skill evaluation. Good congruence was reported of objective scoring and Brachy-PASS (83.4% vs 88%). Ten trainees had performed &lt;15 ICBT, and 28 had performed ≥15 ICBT procedures. Overall 30/38 trainees (78.9%) achieved a Brachy-PASS score of ≥129 (75%). The average score for trainees with &lt;15 procedures was 126.6 (73.6%) vs 148.8 (86.5%) in trainees who performed ≥15 procedures. PGY 4-5 trainees had higher score (153.8 (89.4%) vs 134 (77.9%)). Learning curve threshold of 15 ICBT was identified to attain 75% score (129/172) with no plateauing of learning curve even with <span><math><mo>≥</mo></math></span>30 procedures.</div></div><div><h3>CONCLUSION</h3><div>Competency is established for independently performing intracavitary brachytherapy at 15 procedures and further increase in competency scores continues with increasing procedures.</div></div>","PeriodicalId":55334,"journal":{"name":"Brachytherapy","volume":"24 2","pages":"Pages 339-347"},"PeriodicalIF":1.7,"publicationDate":"2025-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143017625","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Safety and early outcomes of proton therapy and low-dose rate brachytherapy boost for patients with prostate cancer
IF 1.7 4区 医学 Q4 ONCOLOGY Pub Date : 2025-03-01 DOI: 10.1016/j.brachy.2024.12.003
Osama Mohamad , Zakaria El Kouzi , Ramez Kouzy , Seungtaek Choi , Henry Mok , Karen Hoffman , Quynh-Nhu Nguyen , Comron J Hassanzadeh , Chad Tang , Ryan J Park , Shalin Jyotindra Shah , Sean Eric McGuire , Lauren Layer Mayo , Yusung Kim , Surendra Prajapati , Sarath Vijayan , Rajat J Kudchadker , Teresa Lorraine Bruno , Steven Jay Frank

PURPOSE

Brachytherapy boost improves biochemical control for patients with prostate cancer. Here, we report the safety and early efficacy of proton therapy (PT) with a low-dose-rate (LDR) brachytherapy boost.

METHODS

This retrospective study included patients with intermediate- or high-risk prostate cancer treated with PT followed by LDR boost, with or without androgen deprivation therapy (ADT), from 2010 through 2023. Patient, disease, and treatment characteristics, gastrointestinal (GI) and genitourinary (GU) toxicity, and efficacy outcomes are reported.

RESULTS

Ninety-nine patients received PT and LDR boost; median age at diagnosis was 68 years (interquartile range [IQR] 61–72). Most patients (n = 77) were White, 12 were African American, 5 Asian, and 3 Hispanic. Thirty-five patients had intermediate-risk (4 favorable and 31 unfavorable), 56 had high-risk, and 8 had very high-risk disease. Median PT dose was 44 Gy(RBE) (range 40–50.4) and median LDR dose was 90Gy (range 90–110). Pd-103 seed strands were used for 95 patients and I-125 for 4; 90 had MRI-assisted radiosurgery brachytherapy; 91 received ADT; and 21 had a rectal spacer. At a median follow-up time of 45 months, 5-year biochemical recurrence-free survival was 98%. There was no local recurrence, distant metastasis, or cancer death. Four patients had acute urinary retention after brachytherapy procedure. Eleven patients (11%) had late grade 2 GU toxicity, and 3 (3%) had late grade 2 GI toxicity. One patient had grade 3 urethral stricture requiring dilatation and transurethral resection.

CONCLUSIONS

At 45 months' follow-up time, treatment with PT and LDR boost led to high control rates and low toxicity for men with prostate cancer.
{"title":"Safety and early outcomes of proton therapy and low-dose rate brachytherapy boost for patients with prostate cancer","authors":"Osama Mohamad ,&nbsp;Zakaria El Kouzi ,&nbsp;Ramez Kouzy ,&nbsp;Seungtaek Choi ,&nbsp;Henry Mok ,&nbsp;Karen Hoffman ,&nbsp;Quynh-Nhu Nguyen ,&nbsp;Comron J Hassanzadeh ,&nbsp;Chad Tang ,&nbsp;Ryan J Park ,&nbsp;Shalin Jyotindra Shah ,&nbsp;Sean Eric McGuire ,&nbsp;Lauren Layer Mayo ,&nbsp;Yusung Kim ,&nbsp;Surendra Prajapati ,&nbsp;Sarath Vijayan ,&nbsp;Rajat J Kudchadker ,&nbsp;Teresa Lorraine Bruno ,&nbsp;Steven Jay Frank","doi":"10.1016/j.brachy.2024.12.003","DOIUrl":"10.1016/j.brachy.2024.12.003","url":null,"abstract":"<div><h3>PURPOSE</h3><div>Brachytherapy boost improves biochemical control for patients with prostate cancer. Here, we report the safety and early efficacy of proton therapy (PT) with a low-dose-rate (LDR) brachytherapy boost.</div></div><div><h3>METHODS</h3><div>This retrospective study included patients with intermediate- or high-risk prostate cancer treated with PT followed by LDR boost, with or without androgen deprivation therapy (ADT), from 2010 through 2023. Patient, disease, and treatment characteristics, gastrointestinal (GI) and genitourinary (GU) toxicity, and efficacy outcomes are reported.</div></div><div><h3>RESULTS</h3><div>Ninety-nine patients received PT and LDR boost; median age at diagnosis was 68 years (interquartile range [IQR] 61–72). Most patients (<em>n</em> = 77) were White, 12 were African American, 5 Asian, and 3 Hispanic. Thirty-five patients had intermediate-risk (4 favorable and 31 unfavorable), 56 had high-risk, and 8 had very high-risk disease. Median PT dose was 44 Gy(RBE) (range 40–50.4) and median LDR dose was 90Gy (range 90–110). Pd-103 seed strands were used for 95 patients and I-125 for 4; 90 had MRI-assisted radiosurgery brachytherapy; 91 received ADT; and 21 had a rectal spacer. At a median follow-up time of 45 months, 5-year biochemical recurrence-free survival was 98%. There was no local recurrence, distant metastasis, or cancer death. Four patients had acute urinary retention after brachytherapy procedure. Eleven patients (11%) had late grade 2 GU toxicity, and 3 (3%) had late grade 2 GI toxicity. One patient had grade 3 urethral stricture requiring dilatation and transurethral resection.</div></div><div><h3>CONCLUSIONS</h3><div>At 45 months' follow-up time, treatment with PT and LDR boost led to high control rates and low toxicity for men with prostate cancer.</div></div>","PeriodicalId":55334,"journal":{"name":"Brachytherapy","volume":"24 2","pages":"Pages 301-309"},"PeriodicalIF":1.7,"publicationDate":"2025-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143520850","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
From patient to pioneer: The inspiring journey of Dr. Brian Moran
IF 1.7 4区 医学 Q4 ONCOLOGY Pub Date : 2025-03-01 DOI: 10.1016/j.brachy.2024.11.002
Manuj Agarwal , Peter Orio
{"title":"From patient to pioneer: The inspiring journey of Dr. Brian Moran","authors":"Manuj Agarwal ,&nbsp;Peter Orio","doi":"10.1016/j.brachy.2024.11.002","DOIUrl":"10.1016/j.brachy.2024.11.002","url":null,"abstract":"","PeriodicalId":55334,"journal":{"name":"Brachytherapy","volume":"24 2","pages":"Pages 199-209"},"PeriodicalIF":1.7,"publicationDate":"2025-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143025040","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
HDR brachytherapy combined with external beam radiotherapy for unfavorable localized prostate cancer: A single center experience from inception to standard of care
IF 1.7 4区 医学 Q4 ONCOLOGY Pub Date : 2025-03-01 DOI: 10.1016/j.brachy.2024.12.005
Ka-Kit David Yeung , Juanita Crook , Gregory Arbour , Cynthia Araujo , Deidre Batchelar , David Kim , David Petrik , Tracey Rose , Francois Bachand

PURPOSE

High dose rate (HDR) brachytherapy is increasingly adopted for dose escalation in prostate cancer treatment. We report the clinical efficacy and toxicity of HDR prostate brachytherapy combined with external beam radiotherapy (EBRT) and evaluate the predictability of the biochemical definition of cure of 4-year PSA ≤0.2 ng/mL for failure free survival (FFS).

METHODS

A single centre retrospective study was conducted, including all patients with high-tier intermediate risk and high-risk prostate cancer treated with HDR brachytherapy combined with EBRT from 2011 to 2019. Patient and prostate cancer characteristics, treatment, clinical endpoints, and follow up were collected.

RESULTS

Total 319 patients were analyzed. The median age was 68 with median follow up of 77.1 months. Total 142 had high-tier intermediate and 177 had high-risk disease. Brachytherapy doses were initially 20 Gy/2 fractions, and subsequently 15 Gy/1 fraction. All patients received 46 Gy/23 fractions of EBRT. Overall survival at 5 and 9 years was 92.2% and 77.0%, respectively. Failure-free survival (FFS) was 86.0% at 5 years and 76.1% at 9 years. PSA ≤ 0.2 ng/mL at 4 years was seen in 79.3% of patients and was associated with FFS of 94.1% at 9 years. Grade 3 urethral stricture, hematuria, or proctitis occurred in 2.8%, 0%, and 0%, respectively.

CONCLUSION

HDR brachytherapy in addition to EBRT is effective treatment for unfavourable localized prostate cancer with a very acceptable toxicity profile. The biochemical definition of cure of PSA < 0.2 ng/mL at 4 years was predictive for FFS at 9 years.
{"title":"HDR brachytherapy combined with external beam radiotherapy for unfavorable localized prostate cancer: A single center experience from inception to standard of care","authors":"Ka-Kit David Yeung ,&nbsp;Juanita Crook ,&nbsp;Gregory Arbour ,&nbsp;Cynthia Araujo ,&nbsp;Deidre Batchelar ,&nbsp;David Kim ,&nbsp;David Petrik ,&nbsp;Tracey Rose ,&nbsp;Francois Bachand","doi":"10.1016/j.brachy.2024.12.005","DOIUrl":"10.1016/j.brachy.2024.12.005","url":null,"abstract":"<div><h3>PURPOSE</h3><div>High dose rate (HDR) brachytherapy is increasingly adopted for dose escalation in prostate cancer treatment. We report the clinical efficacy and toxicity of HDR prostate brachytherapy combined with external beam radiotherapy (EBRT) and evaluate the predictability of the biochemical definition of cure of 4-year PSA ≤0.2 ng/mL for failure free survival (FFS).</div></div><div><h3>METHODS</h3><div>A single centre retrospective study was conducted, including all patients with high-tier intermediate risk and high-risk prostate cancer treated with HDR brachytherapy combined with EBRT from 2011 to 2019. Patient and prostate cancer characteristics, treatment, clinical endpoints, and follow up were collected.</div></div><div><h3>RESULTS</h3><div>Total 319 patients were analyzed. The median age was 68 with median follow up of 77.1 months. Total 142 had high-tier intermediate and 177 had high-risk disease. Brachytherapy doses were initially 20 Gy/2 fractions, and subsequently 15 Gy/1 fraction. All patients received 46 Gy/23 fractions of EBRT. Overall survival at 5 and 9 years was 92.2% and 77.0%, respectively. Failure-free survival (FFS) was 86.0% at 5 years and 76.1% at 9 years. PSA ≤ 0.2 ng/mL at 4 years was seen in 79.3% of patients and was associated with FFS of 94.1% at 9 years. Grade 3 urethral stricture, hematuria, or proctitis occurred in 2.8%, 0%, and 0%, respectively.</div></div><div><h3>CONCLUSION</h3><div>HDR brachytherapy in addition to EBRT is effective treatment for unfavourable localized prostate cancer with a very acceptable toxicity profile. The biochemical definition of cure of PSA &lt; 0.2 ng/mL at 4 years was predictive for FFS at 9 years.</div></div>","PeriodicalId":55334,"journal":{"name":"Brachytherapy","volume":"24 2","pages":"Pages 318-327"},"PeriodicalIF":1.7,"publicationDate":"2025-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143043966","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Escalating the dose of high-dose-rate brachytherapy combined with external beam radiotherapy improves the disease control rate in patients with high- or very-high-risk prostate cancer 提高高剂量率近距离放疗联合外束放疗的剂量可提高高或极高危前列腺癌患者的疾病控制率。
IF 1.7 4区 医学 Q4 ONCOLOGY Pub Date : 2025-03-01 DOI: 10.1016/j.brachy.2024.10.011
Takaya Inagaki , Yasutaka Noda , Yuya Iwahashi , Takahiro Naka , Maria Kojima , Riki Inagaki , Ryuki Shimono , Azusa Awaya , Yasuo Kohjimoto , Isao Hara , Tetsuo Sonomura

PURPOSE

High-dose-rate brachytherapy (HDR-BT) combined with external beam radiotherapy (EBRT) is an effective treatment for patients with high- and very-high-risk prostate cancer. We sought to identify the factors associated with reduced biochemical recurrence rates following HDR-BT.

METHODS

A total of 304 patients with high- or very-high-risk prostate cancer who underwent HDR-BT and EBRT were analyzed. EBRT comprised 50 Gy in 25 fractions and HDR-BT comprised 18 Gy in 2 fractions. Biochemical recurrence was defined as an increase in prostate specific antigen (PSA) by ≥2.0 ng/mL from the nadir level.

RESULTS

The median follow-up time was 8.2 years (range, 3.4‒13.7 years) after HDR-BT. The 5-year biochemical progression-free survival (bPFS), overall survival, and cause-specific survival rates were 87.4%, 93.3%, and 100%, respectively. In univariate and multivariable analyses, a biologically effective dose (α/β = 1.5) ≥ 240 Gy and androgen deprivation therapy (ADT) were significantly associated with better bPFS (p = 0.020 and 0.007, respectively), whereas pretreatment PSA ≥ 40 ng/mL and Gleason score group 5 were significantly associated with worse bPFS (p = 0.080 and 0.021, respectively). Grade ≥ 3 rectal toxicities occurred in 0.3% of patients and grade ≥ 3 urinary toxicities occurred in 3.4% of patients.

CONCLUSION

In patients with high- and very-high-risk prostate cancer treated with EBRT and HDR-BT, dose escalation and ADT were associated with improved tumor control. By comparison, Gleason score group 5 and pretreatment PSA >40 ng/mL were associated with worse tumor control.
目的:高剂量率近距离放疗(HDR-BT)联合外束放疗(EBRT)是治疗高、高危前列腺癌的有效方法。我们试图确定与HDR-BT后降低生化复发率相关的因素。方法:对304例接受HDR-BT和EBRT治疗的高、高危前列腺癌患者进行分析。EBRT为50 Gy,分为25组,HDR-BT为18 Gy,分为2组。生化复发定义为前列腺特异性抗原(PSA)较最低水平升高≥2.0 ng/mL。结果:HDR-BT后中位随访时间为8.2年(3.4-13.7年)。5年无生化进展生存率(bPFS)、总生存率和病因特异性生存率分别为87.4%、93.3%和100%。在单因素和多变量分析中,生物有效剂量(α/β = 1.5)≥240 Gy和雄激素剥夺治疗(ADT)与较好的bPFS显著相关(p = 0.020和0.007),而预处理PSA≥40 ng/mL和Gleason评分5组与较差的bPFS显著相关(p = 0.080和0.021)。0.3%的患者发生≥3级直肠毒性,3.4%的患者发生≥3级泌尿毒性。结论:在接受EBRT和HDR-BT治疗的高、高危前列腺癌患者中,剂量递增和ADT与肿瘤控制改善相关。相比之下,Gleason评分5组和预处理PSA >40 ng/mL与肿瘤控制较差相关。
{"title":"Escalating the dose of high-dose-rate brachytherapy combined with external beam radiotherapy improves the disease control rate in patients with high- or very-high-risk prostate cancer","authors":"Takaya Inagaki ,&nbsp;Yasutaka Noda ,&nbsp;Yuya Iwahashi ,&nbsp;Takahiro Naka ,&nbsp;Maria Kojima ,&nbsp;Riki Inagaki ,&nbsp;Ryuki Shimono ,&nbsp;Azusa Awaya ,&nbsp;Yasuo Kohjimoto ,&nbsp;Isao Hara ,&nbsp;Tetsuo Sonomura","doi":"10.1016/j.brachy.2024.10.011","DOIUrl":"10.1016/j.brachy.2024.10.011","url":null,"abstract":"<div><h3>PURPOSE</h3><div>High-dose-rate brachytherapy (HDR-BT) combined with external beam radiotherapy (EBRT) is an effective treatment for patients with high- and very-high-risk prostate cancer. We sought to identify the factors associated with reduced biochemical recurrence rates following HDR-BT.</div></div><div><h3>METHODS</h3><div>A total of 304 patients with high- or very-high-risk prostate cancer who underwent HDR-BT and EBRT were analyzed. EBRT comprised 50 Gy in 25 fractions and HDR-BT comprised 18 Gy in 2 fractions. Biochemical recurrence was defined as an increase in prostate specific antigen (PSA) by ≥2.0 ng/mL from the nadir level.</div></div><div><h3>RESULTS</h3><div>The median follow-up time was 8.2 years (range, 3.4‒13.7 years) after HDR-BT. The 5-year biochemical progression-free survival (bPFS), overall survival, and cause-specific survival rates were 87.4%, 93.3%, and 100%, respectively. In univariate and multivariable analyses, a biologically effective dose (α/β = 1.5) ≥ 240 Gy and androgen deprivation therapy (ADT) were significantly associated with better bPFS (<em>p</em> = 0.020 and 0.007, respectively), whereas pretreatment PSA ≥ 40 ng/mL and Gleason score group 5 were significantly associated with worse bPFS (<em>p</em> = 0.080 and 0.021, respectively). Grade ≥ 3 rectal toxicities occurred in 0.3% of patients and grade ≥ 3 urinary toxicities occurred in 3.4% of patients.</div></div><div><h3>CONCLUSION</h3><div>In patients with high- and very-high-risk prostate cancer treated with EBRT and HDR-BT, dose escalation and ADT were associated with improved tumor control. By comparison, Gleason score group 5 and pretreatment PSA &gt;40 ng/mL were associated with worse tumor control.</div></div>","PeriodicalId":55334,"journal":{"name":"Brachytherapy","volume":"24 2","pages":"Pages 223-230"},"PeriodicalIF":1.7,"publicationDate":"2025-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142916566","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
High-dose-rate (2 fractions of 13.5 Gy) and low-dose-rate brachytherapy as monotherapy in prostate cancer. Long term outcomes and predictive value of nadir prostate-specific antigen 高剂量率(2 次,每次 13.5 Gy)和低剂量率近距离放射治疗作为前列腺癌的单一疗法。前列腺特异性抗原最低值的长期疗效和预测价值。
IF 1.7 4区 医学 Q4 ONCOLOGY Pub Date : 2025-03-01 DOI: 10.1016/j.brachy.2024.10.014
Silvia Rodríguez Villalba , Diana Guevara Barrera , Luis Suso-Martí , Enrique Sanchis-Sánchez , Jose Pérez-Calatayud , Jose Domingo Lago Martín , Francisco Blázquez Molina , Manuel Santos Ortega

Purpose

This study aims to evaluate the outcomes of patients treated for low-risk (LR) and favorable intermediate risk (FIR) prostate cancer with brachytherapy (BT) in monotherapy with LDR or HDR and its relationship with nadir PSA (nPSA).

Materials and Methods

We retrospectively analyzed 139 patients (2005-2019) with exclusive LDR (46%. 145/160 Gy) /HDR (54%. 2 implants of 13.5 Gy each separated 10 days). 69% LR and 31% FIR. PSA nadir was grouped into two categories: ≤ 0.2 ng/mL and > 0.2 ng/mL.

Results

Median patient age was 69 years (46-84). Seventy-six patients (55%) received androgen deprivation therapy, and 37% received neoadjuvant therapy. Median follow-up period was 90 months. Actuarial biochemical failure-free survival (BFFS), local control (LC), overall survival (OS), and cause-specific survival (CSS) rates for the total cohort were 78%, 87%, 68%, and 98% at 10 years, respectively. BFFS, LC, OS and CSS in nPSA ≤ 0,2 ng/ml was 90%, 96%, 67%, 100% at 10 years respectively, whereas, those with a nPSA > 0.2 ng/ml had a BFFS, LC, OS and CSS of was 37%, 51%, 72%, 90% at 10 years respectively Statistical significance between both groups was reached in BFFS (p=0,000), LC (p=0,000) and CSS (p=0,007)). In the univariate analysis, there was no difference between risk stratification, BT technique, ADT, or the development of bouncing.

Conclusions

Prostate brachytherapy as monotherapy (LDR and HDR) is an effective treatment option for patients with LR and FIR prostate cancer. nPSA ≤0,2 ng/ml is a representative value that provides prognostic information for favorable outcomes in this group of patients.
目的:本研究旨在评估低风险(LR)和中度风险(FIR)前列腺癌患者接受近距离放射治疗(BT)(LDR或HDR单药治疗)后的疗效,以及其与血中PSA(nPSA)的关系:我们回顾性分析了139例(2005-2019年)接受LDR(46%,145/160 Gy)/HDR(54%,2次植入,每次13.5 Gy,间隔10天)单次治疗的患者。69%为LR,31%为FIR。PSA nadir分为两类:≤ 0.2 ng/mL和> 0.2 ng/mL:患者年龄中位数为 69 岁(46-84 岁)。76名患者(55%)接受了雄激素剥夺治疗,37%接受了新辅助治疗。中位随访期为 90 个月。整个组群的精算无生化失败生存率(BFFS)、局部控制率(LC)、总生存率(OS)和病因特异性生存率(CSS)在10年后分别为78%、87%、68%和98%。nPSA ≤ 0.2 ng/ml 的患者 10 年后的 BFFS、LC、OS 和 CSS 分别为 90%、96%、67% 和 100%,而 nPSA > 0.2 ng/ml 的患者 10 年后的 BFFS、LC、OS 和 CSS 分别为 37%、51%、72% 和 90%,两组患者的 BFFS(P=0,000)、LC(P=0,000)和 CSS(P=0,007)均有统计学意义。)在单变量分析中,风险分层、BT 技术、ADT 或反弹发生率之间没有差异:前列腺近距离放射治疗作为一种单一疗法(LDR 和 HDR)是前列腺癌 LR 和 FIR 患者的有效治疗选择。
{"title":"High-dose-rate (2 fractions of 13.5 Gy) and low-dose-rate brachytherapy as monotherapy in prostate cancer. Long term outcomes and predictive value of nadir prostate-specific antigen","authors":"Silvia Rodríguez Villalba ,&nbsp;Diana Guevara Barrera ,&nbsp;Luis Suso-Martí ,&nbsp;Enrique Sanchis-Sánchez ,&nbsp;Jose Pérez-Calatayud ,&nbsp;Jose Domingo Lago Martín ,&nbsp;Francisco Blázquez Molina ,&nbsp;Manuel Santos Ortega","doi":"10.1016/j.brachy.2024.10.014","DOIUrl":"10.1016/j.brachy.2024.10.014","url":null,"abstract":"<div><h3>Purpose</h3><div>This study aims to evaluate the outcomes of patients treated for low-risk (LR) and favorable intermediate risk (FIR) prostate cancer with brachytherapy (BT) in monotherapy with LDR or HDR and its relationship with nadir PSA (nPSA).</div></div><div><h3>Materials and Methods</h3><div>We retrospectively analyzed 139 patients (2005-2019) with exclusive LDR (46%. 145/160 Gy) /HDR (54%. 2 implants of 13.5 Gy each separated 10 days). 69% LR and 31% FIR. PSA nadir was grouped into two categories: ≤ 0.2 ng/mL and &gt; 0.2 ng/mL.</div></div><div><h3>Results</h3><div>Median patient age was 69 years (46-84). Seventy-six patients (55%) received androgen deprivation therapy, and 37% received neoadjuvant therapy. Median follow-up period was 90 months. Actuarial biochemical failure-free survival (BFFS), local control (LC), overall survival (OS), and cause-specific survival (CSS) rates for the total cohort were 78%, 87%, 68%, and 98% at 10 years, respectively. BFFS, LC, OS and CSS in nPSA ≤ 0,2 ng/ml was 90%, 96%, 67%, 100% at 10 years respectively, whereas, those with a nPSA &gt; 0.2 ng/ml had a BFFS, LC, OS and CSS of was 37%, 51%, 72%, 90% at 10 years respectively Statistical significance between both groups was reached in BFFS (p=0,000), LC (p=0,000) and CSS (p=0,007)). In the univariate analysis, there was no difference between risk stratification, BT technique, ADT, or the development of bouncing.</div></div><div><h3>Conclusions</h3><div>Prostate brachytherapy as monotherapy (LDR and HDR) is an effective treatment option for patients with LR and FIR prostate cancer. nPSA ≤0,2 ng/ml is a representative value that provides prognostic information for favorable outcomes in this group of patients.</div></div>","PeriodicalId":55334,"journal":{"name":"Brachytherapy","volume":"24 2","pages":"Pages 310-317"},"PeriodicalIF":1.7,"publicationDate":"2025-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142824928","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Transition from point A to volume based image guided brachytherapy across a network of centers in India through workshop and mentoring 通过研讨会和指导,从A点过渡到基于体积的图像引导近距离治疗,跨越印度的中心网络。
IF 1.7 4区 医学 Q4 ONCOLOGY Pub Date : 2025-03-01 DOI: 10.1016/j.brachy.2024.11.005
Harjot Kaur Bajwa , Manikumar Singamsetty , Mohan Lal , Manjinder Singh Sidhu , Sumeet Aggarwal , Ritu Agarwal , Midhun Murali , Dhanya K S , Rajesh Natte , Suresh Chaudhari , Vibhor Gupta , Sushil Beriwal

AIM

To demonstrate how workshop and mentoring across a network of radiotherapy centers helped in transitioning from point A to volume-based image guided brachytherapy in carcinoma cervix.

MATERIALS AND METHODS

Based on discussion with different centers across the network, the lapses in cervical cancer treatment were identified and a workshop was designed to change the practice pattern. The main focus of the workshop was to streamline EBRT dose prescription protocols and implement volume based image guided brachytherapy through mentoring and hands on training. Patient data was analyzed 1 year post workshop to assess the impact in changing practice pattern.

RESULTS

A total of 246 cervical cancer patients treated with radical chemo radiotherapy and image guided brachytherapy were analyzed. 207 patients received CT based intracavitary brachytherapy whereas 39 patients received MR based hybrid brachytherapy. In patients who received EBRT and brachytherapy at the same center, the EBRT prescription dose was 45Gy in 25 fractions in 95% patients. The mean dose received by 90% of the HRCTV was 80.8Gy EQD2 in CT based intracavitary brachytherapy and 89.48Gy EQD2 in MR based hybrid brachytherapy. The mean bladder, rectum, sigmoid and small bowel D2cc doses were 63.87Gy, 62.18Gy, 61.2Gy and 55.1Gy EQD2 respectively.

CONCLUSION

This report demonstrates successful implementation and change of carcinoma cervix treatment practice pattern through workshop and mentoring across a network of radiotherapy centers in India.
目的:展示研讨会和指导如何跨越放射治疗中心网络帮助从a点过渡到基于体积的图像引导近距离治疗宫颈癌。材料和方法:通过与网络上不同中心的讨论,确定了宫颈癌治疗的失误,并设计了一个研讨会来改变实践模式。研讨会的主要重点是简化EBRT剂量处方方案,并通过指导和实践培训实施基于体积的图像引导近距离治疗。研究人员分析了讲习班后1年的患者数据,以评估改变实践模式的影响。结果:对246例宫颈癌患者行根治性化疗和影像引导近距离放疗进行分析。207例患者接受基于CT的腔内近距离治疗,39例患者接受基于MR的混合近距离治疗。在同一中心接受EBRT和近距离治疗的患者中,95%的患者的EBRT处方剂量为45Gy,分为25个部分。90% HRCTV的平均剂量为:基于CT的腔内近距离治疗80.8Gy EQD2,基于MR的混合近距离治疗89.48Gy EQD2。膀胱、直肠、乙状结肠和小肠D2cc平均剂量分别为63.87Gy、62.18Gy、61.2Gy和55.1Gy。结论:本报告展示了通过研讨会和指导在印度的放疗中心网络成功实施和改变宫颈癌治疗实践模式。
{"title":"Transition from point A to volume based image guided brachytherapy across a network of centers in India through workshop and mentoring","authors":"Harjot Kaur Bajwa ,&nbsp;Manikumar Singamsetty ,&nbsp;Mohan Lal ,&nbsp;Manjinder Singh Sidhu ,&nbsp;Sumeet Aggarwal ,&nbsp;Ritu Agarwal ,&nbsp;Midhun Murali ,&nbsp;Dhanya K S ,&nbsp;Rajesh Natte ,&nbsp;Suresh Chaudhari ,&nbsp;Vibhor Gupta ,&nbsp;Sushil Beriwal","doi":"10.1016/j.brachy.2024.11.005","DOIUrl":"10.1016/j.brachy.2024.11.005","url":null,"abstract":"<div><h3>AIM</h3><div>To demonstrate how workshop and mentoring across a network of radiotherapy centers helped in transitioning from point A to volume-based image guided brachytherapy in carcinoma cervix.</div></div><div><h3>MATERIALS AND METHODS</h3><div>Based on discussion with different centers across the network, the lapses in cervical cancer treatment were identified and a workshop was designed to change the practice pattern. The main focus of the workshop was to streamline EBRT dose prescription protocols and implement volume based image guided brachytherapy through mentoring and hands on training. Patient data was analyzed 1 year post workshop to assess the impact in changing practice pattern.</div></div><div><h3>RESULTS</h3><div>A total of 246 cervical cancer patients treated with radical chemo radiotherapy and image guided brachytherapy were analyzed. 207 patients received CT based intracavitary brachytherapy whereas 39 patients received MR based hybrid brachytherapy. In patients who received EBRT and brachytherapy at the same center, the EBRT prescription dose was 45Gy in 25 fractions in 95% patients. The mean dose received by 90% of the HRCTV was 80.8Gy EQD2 in CT based intracavitary brachytherapy and 89.48Gy EQD2 in MR based hybrid brachytherapy. The mean bladder, rectum, sigmoid and small bowel D2cc doses were 63.87Gy, 62.18Gy, 61.2Gy and 55.1Gy EQD2 respectively.</div></div><div><h3>CONCLUSION</h3><div>This report demonstrates successful implementation and change of carcinoma cervix treatment practice pattern through workshop and mentoring across a network of radiotherapy centers in India.</div></div>","PeriodicalId":55334,"journal":{"name":"Brachytherapy","volume":"24 2","pages":"Pages 348-353"},"PeriodicalIF":1.7,"publicationDate":"2025-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142901216","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Haralick texture feature analysis for Monte Carlo dose distributions of permanent implant prostate brachytherapy 对永久植入式前列腺近距离放射治疗的蒙特卡洛剂量分布进行哈拉利克纹理特征分析。
IF 1.7 4区 医学 Q4 ONCOLOGY Pub Date : 2025-01-01 DOI: 10.1016/j.brachy.2024.08.256
Iymad R. Mansour , Nelson Miksys , Luc Beaulieu , Éric Vigneault , Rowan M. Thomson

PURPOSE

Demonstrate quantitative characterization of 3D patient-specific absorbed dose distributions using Haralick texture analysis, and interpret measures in terms of underlying physics and radiation dosimetry.

METHODS

Retrospective analysis is performed for 137 patients who underwent permanent implant prostate brachytherapy using two simulation conditions: “TG186” (realistic tissues including 0–3.8% intraprostatic calcifications; interseed attenuation) and “TG43” (water-model; no interseed attenuation). Five Haralick features (homogeneity, contrast, correlation, local homogeneity, entropy) are calculated using the original Haralick formalism, and a modified approach designed to reduce grey-level quantization sensitivity. Trends in textural features are compared to clinical dosimetric measures (D90; minimum absorbed dose to the hottest 90% of a volume) and changes in patient target volume % intraprostatic calcifications by volume (%IC).

RESULTS

Both original and modified measures quantify the spatial differences in absorbed dose distributions. Strong correlations between differences in textural measures calculated under TG43 and TG186 conditions and %IC are observed for all measures. For example, differences between measures of contrast and correlation increase and decrease respectively as patients with higher levels of %IC are evaluated, reflecting the large differences across adjacent voxels (higher absorbed dose in voxels with calcification) when calculated under TG186 conditions. Conversely, the D90 metric is relatively weakly correlated with textural measures, as it generally does not characterize the spatial distribution of absorbed dose.

CONCLUSION

Patient-specific 3D dose distributions may be quantified using Haralick analysis, and trends may be interpreted in terms of fundamental physics. Promising future directions include investigations of novel treatment modalities and clinical outcomes.
目的:利用哈拉利克纹理分析展示三维患者特异性吸收剂量分布的定量特征,并从基础物理学和辐射剂量学的角度解释测量结果:使用两种模拟条件对 137 名接受永久植入式前列腺近距离放射治疗的患者进行回顾性分析:"TG186"(现实组织,包括 0-3.8% 的前列腺内钙化;种间衰减)和 "TG43"(水模型;无种间衰减)。五种哈拉利克特征(均质性、对比度、相关性、局部均质性、熵)采用原始哈拉利克形式和旨在降低灰度级量化敏感性的改进方法进行计算。纹理特征的变化趋势与临床剂量测量(D90;最热 90% 体积的最小吸收剂量)和患者目标体积的变化进行了比较:结果:原始和修改后的测量方法都能量化吸收剂量分布的空间差异。在 TG43 和 TG186 条件下计算的纹理测量值的差异与所有测量值的钙化率之间都存在很强的相关性。例如,在 TG186 条件下计算时,对比度和相关性测量值之间的差异分别随着评估 %IC 水平较高的患者而增大和减小,这反映了相邻体素之间的巨大差异(钙化体素的吸收剂量较高)。相反,D90 指标与纹理测量的相关性相对较弱,因为它通常不能描述吸收剂量的空间分布:结论:使用哈拉利克分析法可以量化特定患者的三维剂量分布,并从基础物理学角度解释其趋势。未来的发展方向包括研究新型治疗模式和临床结果。
{"title":"Haralick texture feature analysis for Monte Carlo dose distributions of permanent implant prostate brachytherapy","authors":"Iymad R. Mansour ,&nbsp;Nelson Miksys ,&nbsp;Luc Beaulieu ,&nbsp;Éric Vigneault ,&nbsp;Rowan M. Thomson","doi":"10.1016/j.brachy.2024.08.256","DOIUrl":"10.1016/j.brachy.2024.08.256","url":null,"abstract":"<div><h3>PURPOSE</h3><div>Demonstrate quantitative characterization of 3D patient-specific absorbed dose distributions using Haralick texture analysis, and interpret measures in terms of underlying physics and radiation dosimetry.</div></div><div><h3>METHODS</h3><div>Retrospective analysis is performed for 137 patients who underwent permanent implant prostate brachytherapy using two simulation conditions: “TG186” (realistic tissues including 0–3.8% intraprostatic calcifications; interseed attenuation) and “TG43” (water-model; no interseed attenuation). Five Haralick features (homogeneity, contrast, correlation, local homogeneity, entropy) are calculated using the original Haralick formalism, and a modified approach designed to reduce grey-level quantization sensitivity. Trends in textural features are compared to clinical dosimetric measures (D90; minimum absorbed dose to the hottest 90% of a volume) and changes in patient target volume % intraprostatic calcifications by volume (%IC).</div></div><div><h3>RESULTS</h3><div>Both original and modified measures quantify the spatial differences in absorbed dose distributions. Strong correlations between differences in textural measures calculated under TG43 and TG186 conditions and %IC are observed for all measures. For example, differences between measures of contrast and correlation increase and decrease respectively as patients with higher levels of %IC are evaluated, reflecting the large differences across adjacent voxels (higher absorbed dose in voxels with calcification) when calculated under TG186 conditions. Conversely, the D90 metric is relatively weakly correlated with textural measures, as it generally does not characterize the spatial distribution of absorbed dose.</div></div><div><h3>CONCLUSION</h3><div>Patient-specific 3D dose distributions may be quantified using Haralick analysis, and trends may be interpreted in terms of fundamental physics. Promising future directions include investigations of novel treatment modalities and clinical outcomes.</div></div>","PeriodicalId":55334,"journal":{"name":"Brachytherapy","volume":"24 1","pages":"Pages 122-133"},"PeriodicalIF":1.7,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142634411","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Impact of MRI-based planning in transperineal interstitial brachytherapy for locally advanced cervix tumors: Clinical, dosimetric and toxicity outcomes 基于磁共振成像的规划对局部晚期宫颈肿瘤经会阴间质近距离治疗的影响:临床、剂量测定和毒性结果。
IF 1.7 4区 医学 Q4 ONCOLOGY Pub Date : 2025-01-01 DOI: 10.1016/j.brachy.2024.10.005
Diana Guevara Barrera , Silvia Rodríguez Villalba , Luis Suso-Martí , Enrique Sanchis-Sánchez , Jose Perez-Calatayud , Jose Domingo Lago Martín , Francisco Blázquez Molina , Manuel Santos Ortega

PURPOSE

To compare dosimetric characteristics, clinical outcomes, and toxicity in patients with locally advanced cervical cancer(LACC) treated with transperineal interstitial brachytherapy(P-ISBT), using CT-based planning or MRI-based planning with a monoinstitutional MRI-compatible applicator, Template Benidorm(TB).

MATERIALS AND METHODS

We retrospectively analyzed 106 women treated with P-ISBT for LACC from 2006 to 2022. P-ISBT was CT-based, with Martinez Universal Perineal Interstitial Template(MUPIT) between 2006 and 2012, or MRI-based planning (TB) since 2013. Volumetric, clinical, and dosimetric parameters were compared between applicators.

RESULTS

Forty-six (43.4%) patients were treated with MUPIT, and 60 (56.6%) with TB. Median follow-up was 42 months (4–188). No significant difference was observed in 5-year local control (LC), regional control (RC), distant failure (DF), overall survival (OS), and disease-specific survival (DSS) between applicators. The TB cohort had fewer needles (p = 0.001), halved median CTV volume (p < 0.001), increased median D90%CTV dose (p < 0.005), and lower D2cc values in rectum/bladder (p < 0.001). G3 chronic toxicity was 15% in the MUPIT group and 6% in TB (p = 0.15), with no G4 toxicity reported. Rectal hemorrhage was lower in the TB group (p = 0.002). Larger CTV volumes correlated with higher rectal D2cc and rectal hemorrhage (p = 0.001; p = 0.029, respectively), and enterovaginal fistula (p = 0.03; p < 0.001, respectively). Median CTV volume was 152.82 cc (35.3–256.78) in patients with chronic rectal toxicity and 102.9 cc (21.4–329.41) in those without (p = 0.001).

CONCLUSION

MRI's superior CTV-volume definition results in smaller treatment volumes, lower D2cc for rectum and bladder, and a trend towards higher CTV D90%. Rectal hemorrhage was significantly lower in the MRI-based group. A significant correlation was observed between larger CTV-volumes, higher rectal D2cc and rectal hemorrhage/enterovaginal fistula.
目的:比较局部晚期宫颈癌(LACC)患者经会阴间质近距离放射治疗(P-ISBT)的剂量学特征、临床疗效和毒性:我们回顾性分析了2006年至2022年期间接受P-ISBT治疗的106名LACC妇女。P-ISBT以CT为基础,在2006年至2012年期间使用马丁内斯通用会阴间质模板(MUPIT),或自2013年起使用基于核磁共振的计划(TB)。对不同应用者的体积、临床和剂量参数进行了比较:46名患者(43.4%)接受了MUPIT治疗,60名患者(56.6%)接受了TB治疗。中位随访时间为 42 个月(4-188 个月)。在 5 年局部控制(LC)、区域控制(RC)、远处失败(DF)、总生存率(OS)和疾病特异性生存率(DSS)方面,观察到不同施用者之间无明显差异。肺结核队列的针数更少(p = 0.001),中位 CTV 容量减半(p < 0.001),中位 D90%CTV 剂量增加(p < 0.005),直肠/膀胱的 D2cc 值降低(p < 0.001)。MUPIT组G3慢性毒性为15%,TB组为6%(p = 0.15),无G4毒性报告。TB组直肠出血较少(p = 0.002)。较大的 CTV 体积与较高的直肠 D2cc 和直肠出血(分别为 p = 0.001;p = 0.029)以及肠瘘(分别为 p = 0.03;p < 0.001)相关。慢性直肠毒性患者的中位CTV体积为152.82cc(35.3-256.78),无慢性直肠毒性患者的中位CTV体积为102.9cc(21.4-329.41)(p = 0.001):结论:磁共振成像对CTV容积的定义更准确,因此治疗容积更小,直肠和膀胱的D2cc更低,CTV D90%也呈上升趋势。MRI 组的直肠出血量明显较低。较大的 CTV 容积、较高的直肠 D2cc 和直肠出血/肠瘘之间存在明显的相关性。
{"title":"Impact of MRI-based planning in transperineal interstitial brachytherapy for locally advanced cervix tumors: Clinical, dosimetric and toxicity outcomes","authors":"Diana Guevara Barrera ,&nbsp;Silvia Rodríguez Villalba ,&nbsp;Luis Suso-Martí ,&nbsp;Enrique Sanchis-Sánchez ,&nbsp;Jose Perez-Calatayud ,&nbsp;Jose Domingo Lago Martín ,&nbsp;Francisco Blázquez Molina ,&nbsp;Manuel Santos Ortega","doi":"10.1016/j.brachy.2024.10.005","DOIUrl":"10.1016/j.brachy.2024.10.005","url":null,"abstract":"<div><h3>PURPOSE</h3><div>To compare dosimetric characteristics, clinical outcomes, and toxicity in patients with locally advanced cervical cancer(LACC) treated with transperineal interstitial brachytherapy(P-ISBT), using CT-based planning or MRI-based planning with a monoinstitutional MRI-compatible applicator, Template Benidorm(TB).</div></div><div><h3>MATERIALS AND METHODS</h3><div>We retrospectively analyzed 106 women treated with P-ISBT for LACC from 2006 to 2022. P-ISBT was CT-based, with Martinez Universal Perineal Interstitial Template(MUPIT) between 2006 and 2012, or MRI-based planning (TB) since 2013. Volumetric, clinical, and dosimetric parameters were compared between applicators.</div></div><div><h3>RESULTS</h3><div>Forty-six (43.4%) patients were treated with MUPIT, and 60 (56.6%) with TB. Median follow-up was 42 months (4–188). No significant difference was observed in 5-year local control (LC), regional control (RC), distant failure (DF), overall survival (OS), and disease-specific survival (DSS) between applicators. The TB cohort had fewer needles (<em>p = 0.001</em>), halved median CTV volume (<em>p &lt; 0.001</em>), increased median D<sub>90%</sub>CTV dose (<em>p &lt; 0.005</em>), and lower D<sub>2cc</sub> values in rectum/bladder (<em>p &lt; 0.001</em>). G3 chronic toxicity was 15% in the MUPIT group and 6% in TB (<em>p = 0.15</em>), with no G4 toxicity reported. Rectal hemorrhage was lower in the TB group (<em>p = 0.002</em>). Larger CTV volumes correlated with higher rectal D2cc and rectal hemorrhage (<em>p = 0.001; p = 0.029</em>, respectively), and enterovaginal fistula (<em>p = 0.03; p &lt; 0.001</em>, respectively). Median CTV volume was 152.82 cc (35.3–256.78) in patients with chronic rectal toxicity and 102.9 cc (21.4–329.41) in those without (<em>p = 0.001</em>).</div></div><div><h3>CONCLUSION</h3><div>MRI's superior CTV-volume definition results in smaller treatment volumes, lower D<sub>2cc</sub> for rectum and bladder, and a trend towards higher CTV D<sub>90%</sub>. Rectal hemorrhage was significantly lower in the MRI-based group. A significant correlation was observed between larger CTV-volumes, higher rectal D<sub>2cc</sub> and rectal hemorrhage/enterovaginal fistula.</div></div>","PeriodicalId":55334,"journal":{"name":"Brachytherapy","volume":"24 1","pages":"Pages 134-143"},"PeriodicalIF":1.7,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142647791","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
期刊
Brachytherapy
全部 Acc. Chem. Res. ACS Applied Bio Materials ACS Appl. Electron. Mater. ACS Appl. Energy Mater. ACS Appl. Mater. Interfaces ACS Appl. Nano Mater. ACS Appl. Polym. Mater. ACS BIOMATER-SCI ENG ACS Catal. ACS Cent. Sci. ACS Chem. Biol. ACS Chemical Health & Safety ACS Chem. Neurosci. ACS Comb. Sci. ACS Earth Space Chem. ACS Energy Lett. ACS Infect. Dis. ACS Macro Lett. ACS Mater. Lett. ACS Med. Chem. Lett. ACS Nano ACS Omega ACS Photonics ACS Sens. ACS Sustainable Chem. Eng. ACS Synth. Biol. Anal. Chem. BIOCHEMISTRY-US Bioconjugate Chem. BIOMACROMOLECULES Chem. Res. Toxicol. Chem. Rev. Chem. Mater. CRYST GROWTH DES ENERG FUEL Environ. Sci. Technol. Environ. Sci. Technol. Lett. Eur. J. Inorg. Chem. IND ENG CHEM RES Inorg. Chem. J. Agric. Food. Chem. J. Chem. Eng. Data J. Chem. Educ. J. Chem. Inf. Model. J. Chem. Theory Comput. J. Med. Chem. J. Nat. Prod. J PROTEOME RES J. Am. Chem. Soc. LANGMUIR MACROMOLECULES Mol. Pharmaceutics Nano Lett. Org. Lett. ORG PROCESS RES DEV ORGANOMETALLICS J. Org. Chem. J. Phys. Chem. J. Phys. Chem. A J. Phys. Chem. B J. Phys. Chem. C J. Phys. Chem. Lett. Analyst Anal. Methods Biomater. Sci. Catal. Sci. Technol. Chem. Commun. Chem. Soc. Rev. CHEM EDUC RES PRACT CRYSTENGCOMM Dalton Trans. Energy Environ. Sci. ENVIRON SCI-NANO ENVIRON SCI-PROC IMP ENVIRON SCI-WAT RES Faraday Discuss. Food Funct. Green Chem. Inorg. Chem. Front. Integr. Biol. J. Anal. At. Spectrom. J. Mater. Chem. A J. Mater. Chem. B J. Mater. Chem. C Lab Chip Mater. Chem. Front. Mater. Horiz. MEDCHEMCOMM Metallomics Mol. Biosyst. Mol. Syst. Des. Eng. Nanoscale Nanoscale Horiz. Nat. Prod. Rep. New J. Chem. Org. Biomol. Chem. Org. Chem. Front. PHOTOCH PHOTOBIO SCI PCCP Polym. Chem.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1