Sylwia Kellas-Sleczka PhD , Stankiewicz Magdalena PhD , Wojcieszek Piotr PhD , Szlag Marta PhD , Lelek Piotr MD , Sleczka Maciej PhD , Cholewka Agnieszka MS
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The inclusion criteria were: ZUBROD 0 or 1, age ≥50 years, pT1-2aN0 cM0, tumor size ≤3 cm, unifocal, invasive carcinoma without neuroinvasion or angioinvasion, with a minimal surgical margin of 2 mm or DCIS with a minimal margin of 5 mm, without extensive intraductal components, positive estrogen receptors. A total dose of 32 Gy in 8 fractions was delivered twice daily with a minimum 6-hour interval. The recommended dose constraints from the Groupe Européen de Curiethérapie and the European Society for Radiotherapy and Oncology (GEC ESTRO) were followed. The primary endpoint was local recurrence.</div></div><div><h3>Results</h3><div>The median age was 65 years (range 46-86 years). The median follow-up was 101 months (range 5-209 months). No serious complications occurred during the procedure and all patients completed the treatment without interruptions. The treatment was well tolerated. In the first 40 cases the 2D treatment planning was used, while in the subsequent cases - 3D treatment planning. The recommended dose-volume limits for the implant, planning target volume (PTV) and organs at risk (OARs) were met. The mean volume of the PTV was 74 cc, with the average coverage with the prescribed dose (PTV ref) of 94%. The mean conformity index (COIN) was 0.69, while the mean dose homogeneity index (DHI) was 0.67. There were no grade ≥ 3 complications. In the whole group, a total of 10 local recurrences (1.96%) were observed. In 3 cases distant metastases (0.6%) and ipsilateral breast tumor recurrence in 8 cases (1.57%) were observed. The 5- and 10-year overall survival (OS) was 97.5% and 96.6%, respectively. The 5- and 10-year disease-free survival (DFS) was 95.6% and 91.3%, respectively.</div></div><div><h3>Conclusions</h3><div>APBI with interstitial multicatheterhigh-dose-rate brachytherapy is a safe and effective treatment, associated with a good toxicity profile and low relapse rates. We believe that patient selection criteria should be revised and possibly expanded. However, further studies are required to validate this approach.</div></div>","PeriodicalId":55334,"journal":{"name":"Brachytherapy","volume":null,"pages":null},"PeriodicalIF":1.7000,"publicationDate":"2024-10-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"BP03 Presentation Time: 4:18 PM\",\"authors\":\"Sylwia Kellas-Sleczka PhD , Stankiewicz Magdalena PhD , Wojcieszek Piotr PhD , Szlag Marta PhD , Lelek Piotr MD , Sleczka Maciej PhD , Cholewka Agnieszka MS\",\"doi\":\"10.1016/j.brachy.2024.08.027\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Purpose</h3><div>The study aims to present the long-term results of 508 cases of early breast cancer treated with accelerated partial breast irradiation (APBI) using interstitial multicatheter high-dose-rate brachytherapy (HDR-BT) following breast-conserving surgery (BCS) in a single institution.</div></div><div><h3>Materials and Methods</h3><div>Between July 2006 and December 2020, a total of 514 cases of low-risk invasive and in situ carcinoma after BCS were treated with APBI using interstitial multicatheter HDR brachytherapy (MIB) at our department and 508 who met the inclusion criteria were analyzed. The inclusion criteria were: ZUBROD 0 or 1, age ≥50 years, pT1-2aN0 cM0, tumor size ≤3 cm, unifocal, invasive carcinoma without neuroinvasion or angioinvasion, with a minimal surgical margin of 2 mm or DCIS with a minimal margin of 5 mm, without extensive intraductal components, positive estrogen receptors. A total dose of 32 Gy in 8 fractions was delivered twice daily with a minimum 6-hour interval. The recommended dose constraints from the Groupe Européen de Curiethérapie and the European Society for Radiotherapy and Oncology (GEC ESTRO) were followed. The primary endpoint was local recurrence.</div></div><div><h3>Results</h3><div>The median age was 65 years (range 46-86 years). The median follow-up was 101 months (range 5-209 months). No serious complications occurred during the procedure and all patients completed the treatment without interruptions. The treatment was well tolerated. In the first 40 cases the 2D treatment planning was used, while in the subsequent cases - 3D treatment planning. The recommended dose-volume limits for the implant, planning target volume (PTV) and organs at risk (OARs) were met. The mean volume of the PTV was 74 cc, with the average coverage with the prescribed dose (PTV ref) of 94%. The mean conformity index (COIN) was 0.69, while the mean dose homogeneity index (DHI) was 0.67. There were no grade ≥ 3 complications. In the whole group, a total of 10 local recurrences (1.96%) were observed. In 3 cases distant metastases (0.6%) and ipsilateral breast tumor recurrence in 8 cases (1.57%) were observed. The 5- and 10-year overall survival (OS) was 97.5% and 96.6%, respectively. The 5- and 10-year disease-free survival (DFS) was 95.6% and 91.3%, respectively.</div></div><div><h3>Conclusions</h3><div>APBI with interstitial multicatheterhigh-dose-rate brachytherapy is a safe and effective treatment, associated with a good toxicity profile and low relapse rates. We believe that patient selection criteria should be revised and possibly expanded. 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The study aims to present the long-term results of 508 cases of early breast cancer treated with accelerated partial breast irradiation (APBI) using interstitial multicatheter high-dose-rate brachytherapy (HDR-BT) following breast-conserving surgery (BCS) in a single institution.
Materials and Methods
Between July 2006 and December 2020, a total of 514 cases of low-risk invasive and in situ carcinoma after BCS were treated with APBI using interstitial multicatheter HDR brachytherapy (MIB) at our department and 508 who met the inclusion criteria were analyzed. The inclusion criteria were: ZUBROD 0 or 1, age ≥50 years, pT1-2aN0 cM0, tumor size ≤3 cm, unifocal, invasive carcinoma without neuroinvasion or angioinvasion, with a minimal surgical margin of 2 mm or DCIS with a minimal margin of 5 mm, without extensive intraductal components, positive estrogen receptors. A total dose of 32 Gy in 8 fractions was delivered twice daily with a minimum 6-hour interval. The recommended dose constraints from the Groupe Européen de Curiethérapie and the European Society for Radiotherapy and Oncology (GEC ESTRO) were followed. The primary endpoint was local recurrence.
Results
The median age was 65 years (range 46-86 years). The median follow-up was 101 months (range 5-209 months). No serious complications occurred during the procedure and all patients completed the treatment without interruptions. The treatment was well tolerated. In the first 40 cases the 2D treatment planning was used, while in the subsequent cases - 3D treatment planning. The recommended dose-volume limits for the implant, planning target volume (PTV) and organs at risk (OARs) were met. The mean volume of the PTV was 74 cc, with the average coverage with the prescribed dose (PTV ref) of 94%. The mean conformity index (COIN) was 0.69, while the mean dose homogeneity index (DHI) was 0.67. There were no grade ≥ 3 complications. In the whole group, a total of 10 local recurrences (1.96%) were observed. In 3 cases distant metastases (0.6%) and ipsilateral breast tumor recurrence in 8 cases (1.57%) were observed. The 5- and 10-year overall survival (OS) was 97.5% and 96.6%, respectively. The 5- and 10-year disease-free survival (DFS) was 95.6% and 91.3%, respectively.
Conclusions
APBI with interstitial multicatheterhigh-dose-rate brachytherapy is a safe and effective treatment, associated with a good toxicity profile and low relapse rates. We believe that patient selection criteria should be revised and possibly expanded. However, further studies are required to validate this approach.
期刊介绍:
Brachytherapy is an international and multidisciplinary journal that publishes original peer-reviewed articles and selected reviews on the techniques and clinical applications of interstitial and intracavitary radiation in the management of cancers. Laboratory and experimental research relevant to clinical practice is also included. Related disciplines include medical physics, medical oncology, and radiation oncology and radiology. Brachytherapy publishes technical advances, original articles, reviews, and point/counterpoint on controversial issues. Original articles that address any aspect of brachytherapy are invited. Letters to the Editor-in-Chief are encouraged.