Radiation Therapy After Upfront Surgery for T1/T2 N0 ER+/PR+/HER2- Breast Cancer
For postmenopausal women with T1/T2 N0 ER+/PR+/HER2- breast cancer after breast-conserving surgery, hypofractionated whole-breast radiation therapy (40-42.5 Gy in 15-16 fractions) is the preferred approach, with a tumor bed boost (10-16 Gy) recommended for higher-risk features including age <50 years or high-grade disease. 1
Standard Whole-Breast Radiation Therapy
Dose and Fractionation
Hypofractionated regimens are preferred over conventional fractionation based on 10-year data from the START trials and Canadian trial showing equivalent local control and superior cosmetic outcomes. 1
- Preferred regimen: 40.0-42.5 Gy in 15-16 fractions over 3.2 weeks 1
- Alternative regimen: 45-50 Gy in 23-25 fractions over 5 weeks 1
The hypofractionated approach reduces radiation-related effects on normal breast tissue including breast shrinkage, telangiectasia, and breast edema compared to conventional fractionation. 1
Tumor Bed Boost
A boost to the tumor bed is strongly recommended for patients with higher-risk features. 1
Indications for boost include:
- Age <50 years 1
- High-grade disease 1
- Positive axillary nodes 1
- Lymphovascular invasion 1
- Focally positive margins (if no re-excision performed) 1
Boost dosing: 10-16 Gy at 2 Gy per fraction, delivered via brachytherapy, electron beam, or photon fields 1
Technical Delivery
Uniform dose distribution and minimal normal tissue toxicity should be achieved using compensators (wedges), forward planning with segments, intensity-modulated radiation therapy (IMRT), respiratory gating, or prone positioning. 1
CT-based treatment planning is encouraged to identify lung and heart volumes and minimize exposure to these organs. 1
Accelerated Partial Breast Irradiation (APBI)
APBI may be considered as an alternative to whole-breast radiation in highly selected low-risk patients, though it remains investigational and enrollment in clinical trials is encouraged. 1, 2
Patient Selection Criteria for APBI
Suitable candidates must meet ALL of the following criteria: 1, 2
- Age ≥60 years
- Not carriers of known BRCA1/2 mutation
- Unifocal, unicentric stage I disease
- ER-positive tumor
- Infiltrating ductal carcinoma or favorable histology
- No extensive intraductal component or LCIS
- Negative surgical margins
- Node-negative (N0)
- Tumor size ≤3 cm 2
APBI Dosing Regimens
Two acceptable regimens exist: 1, 2
- Brachytherapy: 34 Gy in 10 fractions delivered twice per day
- External-beam photon therapy: 38.5 Gy in 10 fractions delivered twice per day
Important Caveats for APBI
- ASTRO stratification guidelines may not adequately predict ipsilateral breast tumor recurrence after APBI 1, 2
- Follow-up data remains limited and studies are ongoing 1, 2
- Intraoperative radiation therapy techniques have shown significantly higher ipsilateral breast cancer recurrence rates compared to whole-breast radiation therapy 2
- Some recent studies document inferior cosmetic outcomes with APBI compared to standard whole-breast radiation 1
Timing of Radiation Therapy
If adjuvant chemotherapy is indicated, radiation should be given after chemotherapy is completed. 1
This recommendation is based on the "Upfront-Outback" trial, though differences in local or distant recurrence were not statistically significant at 135-month follow-up. 1
Sequential administration of chemotherapy followed by endocrine therapy, then radiation is acceptable. 1
Regional Nodal Irradiation
For T1/T2 N0 disease, regional nodal irradiation is NOT routinely indicated. 1
Regional nodal radiation is reserved for patients with positive lymph nodes (1-3 positive nodes or high-risk node-negative disease), which does not apply to the N0 population in this question. 1
Practical Algorithm Summary
For your postmenopausal T1/T2 N0 ER+/PR+/HER2- patient after breast-conserving surgery:
- Standard approach: Hypofractionated whole-breast RT (40-42.5 Gy in 15-16 fractions) 1
- Add tumor bed boost (10-16 Gy) if high-grade disease present 1
- Consider APBI only if patient meets ALL strict selection criteria (age ≥60, unifocal, ≤3 cm, favorable histology) and preferably within a clinical trial 1, 2
- Deliver radiation after completion of any adjuvant chemotherapy 1