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Breast boost using noninvasive image-guided breast brachytherapy vs. external beam: a 2:1 matched-pair analysis
Kara Lynne Leonard1, Jaroslaw T Hepel, John R Styczynski
1Department of Radiation Oncology, Rhode Island Hospital, Brown Alpert Medical School, Providence, RI; Department of Radiation Oncology, Tufts Medical Center, Tufts University School of Medicine, Boston, MA.
NIBB boost shows better short-term outcomes than external beam (EB) boost for early-stage breast cancer patients. This study found significantly less skin toxicity with NIBB compared to EB boost.
Area of Science:
- Oncology
- Radiation Oncology
- Breast Cancer Treatment
Background:
- External beam (EB) boost and Norwood Interstitial Brachytherapy Boost (NIBB) boost are used in early-stage breast cancer treatment.
- Comparing clinical outcomes and toxicity between these boost techniques is crucial for treatment optimization.
Purpose of the Study:
- To compare clinical outcomes and toxicity in patients receiving NIBB boost versus EB boost for early-stage breast cancer.
- To evaluate the safety and efficacy of NIBB boost in comparison to conventional EB boost techniques.
Main Methods:
- A retrospective analysis compared 47 women treated with NIBB boost to 94 matched controls treated with EB boost (electron or 3-D conformal radiation).
- Patients were matched based on age, stage, chemotherapy use, and fractionation.
- Acute and late toxicity, as well as oncologic outcomes, were reviewed using the McNemar nonparametric test.
Main Results:
- Grade 2+ desquamation occurred in 39% of NIBB patients versus 52% of EB patients (P = .07).
- Predictors for acute desquamation included breast size, electron energy, and fractionation.
- Significantly less combined skin/subcutaneous toxicity (P = .046) was observed in the NIBB group, with only 2% developing Grade 2+ fibrosis compared to 9.5% in the EB group.
Conclusions:
- NIBB boost is associated with favorable short-term clinical outcomes compared to EB boost.
- NIBB boost demonstrates a potential for reduced late toxicity, specifically skin/subcutaneous fibrosis.
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