Is accelerated partial‑breast irradiation appropriate for a 55‑year‑old woman with a 1.8 cm, estrogen‑receptor‑positive, node‑negative, unifocal invasive breast carcinoma with clear surgical margins (≥2 mm) after breast‑conserving surgery?

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Last updated: February 24, 2026View editorial policy

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Accelerated Partial Breast Irradiation for This Patient

Yes, APBI is appropriate for this 55-year-old woman with a 1.8 cm, ER-positive, node-negative, unifocal invasive breast carcinoma with clear surgical margins ≥2 mm after breast-conserving surgery. She meets all the established criteria for APBI as defined by current national guidelines.

Patient Eligibility Assessment

This patient satisfies the NCCN-endorsed ASTRO consensus criteria for patients "suitable" for APBI 1:

  • Age ≥50 years (patient is 55 years old) 1, 2
  • Invasive ductal carcinoma ≤2 cm (T1 disease; patient has 1.8 cm tumor) 1, 2
  • Negative margins by ≥2 mm (patient meets this criterion) 1, 2
  • Hormone receptor-positive (patient is ER-positive) 1, 2
  • Node-negative disease (N0) 1, 2
  • Unifocal disease (patient has unifocal tumor) 2

The European Society for Medical Oncology 2024 guidelines further support APBI for patients with tumor size ≤3 cm, which this patient clearly meets 2.

Recommended APBI Regimens

Two evidence-based treatment options are available 1, 2, 3:

Brachytherapy approach:

  • 34 Gy in 10 fractions delivered twice daily 1, 2, 3

External beam radiation therapy approach:

  • 38.5 Gy in 10 fractions delivered twice daily 1, 2, 3

Both regimens target the tumor bed and are delivered over approximately 5-8 days 4.

Evidence Supporting APBI in This Population

Non-inferiority has been demonstrated: A randomized study of APBI using interstitial brachytherapy versus whole breast radiation therapy showed APBI was not inferior to WBRT with respect to 5-year local control, disease-free survival, and overall survival 1. The RAPID trial confirmed non-inferiority with 8-year cumulative ipsilateral breast tumor recurrence rates of 3.0% for APBI versus 2.8% for whole breast irradiation (HR 1.27,90% CI 0.84-1.91) 4.

Long-term outcomes are favorable: The NSABP B-39 trial demonstrated 10-year IBTR rates of 4.6% with APBI versus 3.9% with whole breast irradiation, with overall low recurrence rates in both arms 5.

Important Caveats

Cosmetic outcomes require attention to technique: The RAPID trial showed increased late toxicity and worse cosmesis with twice-daily external beam APBI (17.7% adverse cosmesis at 7 years) 4, 5. This appears related to the twice-daily fractionation schedule 4, 5.

Alternative fractionation schemes may improve outcomes: Once-daily APBI regimens are under investigation and may provide better cosmetic results 1, 5. A novel once-daily scheme of 49.95 Gy in 15 fractions demonstrated 93.5% 12-year ipsilateral breast recurrence-free survival with 91% excellent-to-good cosmesis 6.

Brachytherapy may offer superior cosmesis: Interstitial brachytherapy showed similar toxicity profiles and cosmetic results to whole breast irradiation at 5 years, with fewer grade 2/3 late skin side effects 1. The American Brachytherapy Society identifies interstitial brachytherapy as having the strongest evidence among APBI techniques 7.

Ensure complete target coverage: Any APBI technique must allow full coverage of the entire target volume, typically 1-1.5 cm beyond the surgical cavity 2, 8. CT-based treatment planning is essential 3.

Clinical Trial Participation

While APBI is now guideline-endorsed for suitable patients like this one, the NCCN still encourages participation in high-quality prospective clinical trials when available, as some aspects remain investigational 1, 3.

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Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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