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Accelerated Partial Breast Irradiation (APBI): Where Are We Now?
Mira Goldberg1, Timothy J Whelan1
1Department of Oncology, McMaster University and Juravinski Cancer Centre, 699 Concession Street, Hamilton, ON L8V 5C2 Canada.
Current Breast Cancer Reports
|October 26, 2020
Summary
Accelerated partial breast irradiation (APBI) offers a convenient alternative to whole breast irradiation (WBI), with comparable local recurrence rates. However, careful patient selection is crucial due to potential differences in toxicity and cosmetic outcomes.
Area of Science:
- Oncology
- Radiation Oncology
- Breast Cancer Treatment
Background:
- Accelerated partial breast irradiation (APBI) is a time-efficient alternative to whole breast irradiation (WBI) in breast conserving therapy.
- APBI techniques include brachytherapy, intraoperative radiation, and external beam radiation therapy (EBRT).
- This review evaluates recent randomized controlled trials (RCTs) on APBI and their clinical implications.
Purpose of the Study:
- To appraise the latest modern randomized controlled trials (RCTs) of accelerated partial breast irradiation (APBI).
- To discuss the application of APBI data to clinical practice.
- To compare APBI outcomes with whole breast irradiation (WBI).
Main Methods:
- Review of recent randomized controlled trials (RCTs) including OCOG-RAPID, NSABP B-39/RTOG 0413, and University of Florence studies.
- Analysis of long-term outcomes, including ipsilateral breast tumor recurrence (IBTR), toxicity, and cosmetic results.
- Evaluation of different APBI delivery techniques (EBRT, brachytherapy) and fractionation schedules.
Main Results:
- The OCOG-RAPID trial showed non-inferiority of APBI to WBI in terms of IBTR (8-year rates: 3% vs. 2.8%), but with worse late toxicity and cosmesis.
- The NSABP B-39 trial, including higher-risk patients, did not demonstrate equivalence, with 10-year IBTR rates of 4.6% for APBI vs. 3.9% for WBI.
- The University of Florence study reported low 10-year local recurrence rates and excellent cosmetic outcomes with a specific EBRT fractionation (30 Gy/5 fractions).
Conclusions:
- APBI integration into practice requires careful patient selection, favoring low-risk ductal carcinoma in situ or early-stage (T1) invasive ductal cancer with favorable characteristics.
- Optimal dose and fractionation for EBRT-based APBI require further research.
- APBI offers improved patient convenience and cost savings compared to WBI when appropriately applied.
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