A Single-Institution Review of Accelerated Partial Breast Irradiation in Patients Considered “Cautionary” by the American Society for Radiation Oncology

2011 ◽  
Vol 19 (2) ◽  
pp. 553-559 ◽  
Author(s):  
Tari S. Stull ◽  
M. Catherine Goodwin ◽  
Edward J. Gracely ◽  
Michael R. Chernick ◽  
Richard J. Carella ◽  
...  
2018 ◽  
Vol 84 (8) ◽  
pp. 1261-1263
Author(s):  
Anthony M. Scott ◽  
Matthew C. Callier ◽  
Madison Lashley ◽  
David A. Cole ◽  
Paul S. Dale

Accelerated partial breast irradiation (APBI) using the implanted brachytherapy device MammoSite® was approved for routine use by the Food and Drug Administration in 2002. The American Society of Breast Surgeons MammoSite® Breast Brachytherapy Registry served as a guideline for our institution to begin offering this treatment in 2005. This report reviews our available data to provide an analysis of patient outcomes over 12 years of use at a single institution. A retrospective review was conducted of records of 150 patients who underwent APBI or attempted APBI after breast-sparing surgeries between 2006 and 2017. These charts were analyzed for documentation of patient age, cancer stage, incidence of recurrence, and posttreatment complications. Of the patients evaluated, 99 per cent (149/150) completed treatment. The median time since treatment completion is now 8.9 years. One hundred eleven patients (74%) are now greater than five years posttreatment. Ipsilateral breast recurrence was found in 2.7 per cent of patients (4/149), and 1.3 per cent of patients (2/149) developed new primary breast tumors. Acute complications, mostly skin erythema (21%), were uncommon and self-limited. Subacute effects were generally fibrosis (13%) and mild local pain (9.4%). APBI for breast cancer after breast-conserving surgery continues to be used at our institution for select patients with good outcomes. Local control and toxicity are similar to that reported in the literature. Five-year local recurrence rates compare favorably with national trials. Occasional complications included fibrosis, persistent pain, and skin irritation.


2011 ◽  
Vol 29 (27_suppl) ◽  
pp. 84-84
Author(s):  
J. A. Hattangadi ◽  
N. Taback ◽  
B. A. Neville ◽  
J. R. Harris ◽  
R. S. Punglia

84 Background: APBIb is a novel alternative to whole breast irradiation (WBI). The American Society for Radiation Oncology Guidelines (ASTRO-G) established appropriateness for APBIb use off protocol. Methods: 138,815 bca patients from the Surveillance, Epidemiology, and End Results database underwent WBI or APBIb after lumpectomy from 2000 to 2007. Patients were classified as suitable, cautionary, or unsuitable for APBIb according to ASTRO-G. Logistic regression was applied to study APBIb use overall and within each guideline category. Results: Overall, 2.6% received APBIb and use varied by ASTRO-G: 5% in suitable, 3.4% in cautionary, and 1.6% in unsuitable patients (p<0.0001). APBIb use increased with time (2000: 0.3%, 2007: 7%) and varied widely with region (0% Alaska; 7% Atlanta, Georgia). Independent predictors of APBIb among suitable patients included white (OR 2.0, p<0.001) race, region (OR 2.6-8.6, p<0.0001), later year (2006-7 v 2000-2 OR 20.3, p<0.0001), and lower grade (OR 1.3, p=0.01). Among cautionary patients, white race (OR 1.8, p<0.001), non-Hispanic ethnicity (OR 1.3, p<0.04), region (OR 3.1-10.2, p<0.0001), metropolitan location (OR 1.9, p=0.01), later year (2006-2007 OR 17.6, p<0.0001), and lower grade (OR 1.4, p<0.0001) predicted for APBIb. Among unsuitable patients, race (p<0.0001), region (OR 3.3-21.6, p<0.0001), later year (2006-7 OR 12.7, p<0.0001), estrogen receptor-positive status (OR 1.3, p=0.002), lower grade (OR 1.3, p<0.01), and negative lymph nodes (OR 2.0, p<0.0001) predicted for use. In several regions, odds of APBIb increased as appropriateness decreased (see Table). Conclusions: APBIb has been rapidly adopted in the US. Its use varied by race, ethnicity, and region, especially among patients who may not be suitable candidates for this technique. [Table: see text]


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