Intraoperative radiotherapy boost as part of breast-conservation therapy for breast cancer: a single-institution retrospective analysis

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Názov: Intraoperative radiotherapy boost as part of breast-conservation therapy for breast cancer: a single-institution retrospective analysis
Autori: Stoian, Raluca, Erbes, Thalia, Zamboglou, Constantinos, Scholber, Jutta Ursula, Gainey, Mark, Sachpazidis, Ilias, Haehl, Erik, Spohn, Simon, Verma, Vivek, Krug, David, Rühle, Alexander, Juhasz-Böss, Ingolf, Grosu, Anca-Ligia, Nicolay, Nils H., Sprave, Tanja
Zdroj: Strahlenther Onkol
Informácie o vydavateľovi: Springer Science and Business Media LLC, 2021.
Rok vydania: 2021
Predmety: Female [MeSH], Mastectomy, Segmental [MeSH], Radiotherapy, Adjuvant/methods [MeSH], Adjuvant radiation therapy, Humans [MeSH], Breast Neoplasms/drug therapy [MeSH], Retrospective Studies [MeSH], Breast Neoplasms/radiotherapy [MeSH], Boost, Original Article, Early breast cancer, Breast-conservation therapy, Neoplasm Recurrence, Local [MeSH], Breast Neoplasms/surgery [MeSH], Breast/radiation effects [MeSH], Intraoperative radiotherapy, Breast Neoplasms, Mastectomy, Segmental, 3. Good health, 03 medical and health sciences, 0302 clinical medicine, Humans, Female, Radiotherapy, Adjuvant, Breast, Neoplasm Recurrence, Local, Retrospective Studies
Popis: Background There are currently no data from randomized controlled trials on the use of intraoperative radiotherapy (IORT) as a tumor bed boost as part of a breast-conservation approach for breast cancer. This study retrospectively reviewed the safety and efficacy of IORT as a boost treatment at a tertiary cancer center. Methods From 2015 to 2019, patients underwent breast-conserving surgery with axillary lymph node staging and a single dose of 20 Gy IORT with 50-kV photons, followed by whole-breast irradiation (WBI) and adjuvant systemic therapy (if applicable). Patients were followed for assessment of acute and late toxicities (using the Common Terminology Criteria for Adverse Events version 5.0) at 3–6-month intervals. Outcomes included ipsilateral (IBTR) and contralateral breast progression-free survival (CBE), distant metastasis-free survival (DMFS), and overall survival (OS). Results Median follow-up for the 214 patients was 28 (range 2–59) months. Most patients had T1 disease (n = 124) and were clinically node negative. Only few patients had high-grade and/or triple-negative disease. The vast majority of patients underwent sentinel node biopsy, and 32 (15%) required re-resection for initially positive margins. Finally, all tumor bed margins were clear. Nine (4.2%) and 48 (22.4%) patients underwent neoadjuvant and adjuvant chemotherapy, respectively. WBI was predominantly performed as conventionally fractionated WBI (n = 187, 87.4%), and the median time from BCS to WBI was 54.5 days. IORT was delivered with a single dose of 20 Gy. The median WBI dose was 50 Gy (range 29.4–50.4 Gy). No patients experienced grade 4 events; acute grade 3 toxicities were limited to 17 (8%) cases of radiation dermatitis. Postoperative toxicities were mild. After WBI only one case of late grade ≥ 2 events was reported. There were two recurrences in the tumor bed and one contralateral breast event. Conclusion This investigation provides additional preliminary data supporting the using of IORT in the boost setting and corroborates the existing literature. These encouraging results should be prospectively validated by the eventual publication of randomized studies such as TARGIT‑B.
Druh dokumentu: Article
Other literature type
Popis súboru: pdf
Jazyk: English
ISSN: 1439-099X
0179-7158
DOI: 10.1007/s00066-021-01785-2
Prístupová URL adresa: https://link.springer.com/content/pdf/10.1007/s00066-021-01785-2.pdf
https://pubmed.ncbi.nlm.nih.gov/33938966
https://link.springer.com/content/pdf/10.1007/s00066-021-01785-2.pdf
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8397646
https://europepmc.org/article/MED/33938966
https://link.springer.com/article/10.1007/s00066-021-01785-2
https://repository.publisso.de/resource/frl:6448667
Rights: CC BY
Prístupové číslo: edsair.doi.dedup.....9a2cbb1589ae335633aab75bdf1e4e93
Databáza: OpenAIRE
Popis
Abstrakt:Background There are currently no data from randomized controlled trials on the use of intraoperative radiotherapy (IORT) as a tumor bed boost as part of a breast-conservation approach for breast cancer. This study retrospectively reviewed the safety and efficacy of IORT as a boost treatment at a tertiary cancer center. Methods From 2015 to 2019, patients underwent breast-conserving surgery with axillary lymph node staging and a single dose of 20 Gy IORT with 50-kV photons, followed by whole-breast irradiation (WBI) and adjuvant systemic therapy (if applicable). Patients were followed for assessment of acute and late toxicities (using the Common Terminology Criteria for Adverse Events version 5.0) at 3–6-month intervals. Outcomes included ipsilateral (IBTR) and contralateral breast progression-free survival (CBE), distant metastasis-free survival (DMFS), and overall survival (OS). Results Median follow-up for the 214 patients was 28 (range 2–59) months. Most patients had T1 disease (n = 124) and were clinically node negative. Only few patients had high-grade and/or triple-negative disease. The vast majority of patients underwent sentinel node biopsy, and 32 (15%) required re-resection for initially positive margins. Finally, all tumor bed margins were clear. Nine (4.2%) and 48 (22.4%) patients underwent neoadjuvant and adjuvant chemotherapy, respectively. WBI was predominantly performed as conventionally fractionated WBI (n = 187, 87.4%), and the median time from BCS to WBI was 54.5 days. IORT was delivered with a single dose of 20 Gy. The median WBI dose was 50 Gy (range 29.4–50.4 Gy). No patients experienced grade 4 events; acute grade 3 toxicities were limited to 17 (8%) cases of radiation dermatitis. Postoperative toxicities were mild. After WBI only one case of late grade ≥ 2 events was reported. There were two recurrences in the tumor bed and one contralateral breast event. Conclusion This investigation provides additional preliminary data supporting the using of IORT in the boost setting and corroborates the existing literature. These encouraging results should be prospectively validated by the eventual publication of randomized studies such as TARGIT‑B.
ISSN:1439099X
01797158
DOI:10.1007/s00066-021-01785-2