Three-Fraction Accelerated Partial Breast Irradiation (APBI) Delivered With Brachytherapy Applicators Is Feasible and Safe: First Results From the TRIUMPH-T Trial

التفاصيل البيبلوغرافية
العنوان: Three-Fraction Accelerated Partial Breast Irradiation (APBI) Delivered With Brachytherapy Applicators Is Feasible and Safe: First Results From the TRIUMPH-T Trial
المؤلفون: Catheryn M. Yashar, Doug Arthur, Roger G. Dale, Robert R. Kuske, Peter Y. Chen, Bruce G. Haffty, Matthew M. Poppe, Zeinab Abou Yehia, Atif J. Khan, Linna Li, Chirag Shah, Frank A. Vicini, Dirk F. Moore
المصدر: Int J Radiat Oncol Biol Phys
سنة النشر: 2019
مصطلحات موضوعية: Cancer Research, medicine.medical_specialty, Radiation, business.industry, medicine.medical_treatment, Brachytherapy, Lumpectomy, Dose fractionation, Partial Breast Irradiation, medicine.disease, Article, 030218 nuclear medicine & medical imaging, Metastasis, Clinical trial, 03 medical and health sciences, 0302 clinical medicine, Oncology, 030220 oncology & carcinogenesis, medicine, Radiology, Nuclear Medicine and imaging, Radiology, Prospective cohort study, business, Mastectomy
الوصف: Purpose Shorter courses of accelerated partial-breast irradiation delivered as single-fraction intraoperative therapy are now offered as an alternative to 4 to 6 weeks of whole-breast irradiation after lumpectomy. However, this approach has potential shortcomings in patient selection and target volume definition and in dosimetric, radiobiological, and logistical issues. We designed a prospective, phase 2, multi-institution clinical trial to study 2- or 3-day accelerated partial breast irradiation delivered with brachytherapy applicators. Methods and Materials This trial treats select breast cancers after breast-conserving surgery with brachytherapy applicators that deliver 22.5 Gy in 3 fractions of 7.5 Gy. The planning treatment volume was 1 to 1.5 cm beyond the surgical cavity. Eligible women were aged ≥45 years with unicentric invasive or in situ tumors ≤3.0 cm with positive estrogen or progesterone receptors and no metastasis to axillary nodes that have been excised with negative margins. Strict dosimetric parameters were required to be met before acceptance into the trial. Results A group of 200 patients was prospectively enrolled and followed for a minimum of 6 months. Two- or 3-day brachytherapy was associated with low acute or subacute toxicity, 97.25% excellent or good cosmetic outcomes, and excellent local control in select breast cancers. Conclusions Ultrashort breast brachytherapy is dosimetrically feasible and can be delivered with excellent short-term tolerance and low toxicity.
اللغة: English
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8c2fb0097dd2139e95cbe76859fe3cdd
https://europepmc.org/articles/PMC7373303/
Rights: OPEN
رقم الانضمام: edsair.doi.dedup.....8c2fb0097dd2139e95cbe76859fe3cdd
قاعدة البيانات: OpenAIRE