Phase 2 Trial of Accelerated Partial Breast Irradiation (APBI) Using Noninvasive Image Guided Breast Brachytherapy (NIBB).
Aged
Aged, 80 and over
Brachytherapy
/ adverse effects
Breast
Breast Diseases
/ etiology
Breast Neoplasms
/ pathology
Carcinoma, Intraductal, Noninfiltrating
/ pathology
Dose Fractionation, Radiation
Female
Humans
Immobilization
/ methods
Iridium Radioisotopes
/ adverse effects
Middle Aged
Neoplasm Recurrence, Local
Prospective Studies
Radiotherapy, Image-Guided
/ methods
Telangiectasis
/ etiology
Treatment Outcome
Journal
International journal of radiation oncology, biology, physics
ISSN: 1879-355X
Titre abrégé: Int J Radiat Oncol Biol Phys
Pays: United States
ID NLM: 7603616
Informations de publication
Date de publication:
01 12 2020
01 12 2020
Historique:
received:
28
04
2020
revised:
17
07
2020
accepted:
23
07
2020
pubmed:
30
7
2020
medline:
16
4
2021
entrez:
30
7
2020
Statut:
ppublish
Résumé
Noninvasive image guided breast brachytherapy (NIBB) is a novel approach to delivery of accelerated partial breast irradiation (APBI) that may hold advantages over established techniques. NIBB is not invasive but maintains a high level of precision by using breast immobilization via breast compression and image guidance; it therefore does not require large planning tumor volume margins. We present the primary outcomes of this prospective phase 2 study (BrUOG Br-251). Eligible patients with early-stage breast cancer underwent NIBB APBI using a dose 34 Gy in 10 fractions delivered daily or twice a day. Treatment was delivered using an Ir-192 high-dose-rate source via specialized applicators. Two orthogonal treatment axes were used for each fraction. The primary endpoints were late toxicity and cosmesis assessed at 2 and 5 years. Toxicity was assessed using the National Cancer Institute Common Terminology Criteria for Adverse Events v3.0. Cosmesis was assessed using the NRG/Radiation Therapy Oncology Group scale. Ipsilateral breast tumor recurrence was defined as any recurrence or new primary in the treated breast. Forty patients underwent protocol treatment. Median patient age was 68 years (50-92 years). Mean tumor size was 1.1 cm (0.3-3.0 cm). Among the cohort, 62.5% had invasive carcinoma and 37.5% had ductal carcinoma in situ. Thirty-nine percent elected to receive hormone therapy. No grade ≥3 late toxicities were observed at any time point. Grade 2 toxicity was 5% and 10% at 2 and 5 years, respectively. Telangiectasia grade 1 and 2 occurred in 27.5% and 5%, respectively. Breast separation of >7 cm was associated with telangiectasia (P < .01). The rate of good to excellent cosmetic outcome was 95% at 2 years and 100% at 5 years. With a median follow-up of 68 months, the actuarial 5-year freedom from ipsilateral breast tumor recurrence was 93.3% (±4.8%), and overall survival was 93.7% (±4.4%). NIBB to deliver APBI is well tolerated with a low incidence of significant late toxicity and has favorable cosmetic outcomes. Continued evaluation of the NIBB APBI technique in a larger cohort is warranted.
Identifiants
pubmed: 32721422
pii: S0360-3016(20)33731-7
doi: 10.1016/j.ijrobp.2020.07.2312
pii:
doi:
Substances chimiques
Iridium Radioisotopes
0
Banques de données
ClinicalTrials.gov
['NCT01463007']
Types de publication
Clinical Trial, Phase II
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
1143-1149Informations de copyright
Copyright © 2020 Elsevier Inc. All rights reserved.