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Dose Deintensified 3-Day Photon, Proton, or Brachytherapy: A Nonrandomized Controlled Partial Breast Irradiation Trial

  • Robert W. Mutter
  • , Michael A. Golafshar
  • , Matthew R. Buras
  • , Bryce P. Comstock
  • , Maddi Jacobson
  • , Todd DeWees
  • , Nicholas B. Remmes
  • , Leah N. Francis
  • , Judy C. Boughey
  • , Kathryn J. Ruddy
  • , Lisa A. McGee
  • , Arslan Afzal
  • , Laura A. Vallow
  • , Keith M. Furutani
  • , Christopher L. Deufel
  • , Dean A. Shumway
  • , Haeyoung Kim
  • , Minetta C. Liu
  • , Amy C. Degnim
  • , James W. Jakub
  • Tamara Z. Vern-Gross, William W. Wong, Samir H. Patel, Carlos E. Vargas, Bradley J. Stish, Mark R. Waddle, Deanna H. Pafundi, Michele Y. Halyard, Kimberly S. Corbin, Tina J. Hieken, Sean S. Park
  • Mayo Clinic Rochester, MN
  • Mayo Clinic Graduate School of Biomedical Sciences
  • Mayo Clinic Scottsdale-Phoenix, Arizona
  • Mayo Clinic in Jacksonville, Florida

Research output: Contribution to journal › Article › peer-review

Abstract

Purpose: The optimal approach for partial breast irradiation (PBI) is unknown. We investigated a novel de-intensified 3-fraction PBI regimen for photons, protons, and brachytherapy. Methods and Materials: A multicenter nonrandomized controlled trial with the primary outcome of adverse cosmesis at 3 years versus before PBI. Eligibility criteria were age ≥50 years treated with breast-conserving surgery for node-negative estrogen receptor–positive (ER+) invasive breast cancer or any ductal carcinoma in situ (DCIS) measuring ≤2.5 cm. Photon and proton PBI were prescribed 21.9 Gy (relative biological effectiveness) and brachytherapy 21 Gy in 3 fractions. Radiation therapy technique and adjuvant endocrine therapy were selected at physician and patient discretion. Results: Between June 17, 2015, and July 13, 2017, 161 eligible patients were treated with photons (56), protons (49), or brachytherapy (56). Median patient age was 66.8 years. One hundred twenty-six (78.3%) had invasive breast cancer (all ER+) and 35 (21.7%) had DCIS (88.6% ER+). Fifty-four percent of patients with invasive breast cancer and 25.8% of patients with ER+ DCIS initiated and adhered to the prescribed endocrine therapy. The proportion of patients with adverse cosmesis (by trained nurse assessment) was 14.5% at baseline and 2.3% at 3 years (difference, −12.2%; 95% CI, −100% to −6.4%). Adverse cosmesis at the last follow-up, with a median follow-up of 5 years, was 5.7% by nurse assessment, 5.6% by panel assessment of digital photographs, and 5.2% by patient self-report. There were no observed clinically meaningful changes in other patient-reported outcomes, and just 2 grade 2 or higher adverse events, both grade 2, in the brachytherapy cohort. Five-year local recurrence–free survival and progression-free survival were 98.0% and 95.5%, respectively. There were no local recurrences among 60 patients with invasive breast cancer and Ki67 ≤13.25%. Conclusions: Deintensified 3-day PBI provided favorable disease control, tolerability, and cosmetic outcomes, meeting the prespecified criteria for acceptability. This approach is an attractive option for patients with small node-negative ER+ breast cancer and DCIS.

Original languageEnglish
Pages (from-to)352-364
Number of pages13
JournalInternational Journal of Radiation Oncology Biology Physics
Volume121
Issue number2
DOIs
StatePublished - 1 Feb 2025

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

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