MedPath

NRG Oncology Trial Shows Regional Nodal Radiation Provides No Benefit for Breast Cancer Patients with Node Conversion After Neoadjuvant Chemotherapy

25 days ago4 min read
Share

Key Insights

  • The NRG-NSABP B-51/RTOG 1304 trial found that regional nodal irradiation does not reduce invasive breast cancer recurrence in patients whose axillary nodes converted from positive to negative after neoadjuvant chemotherapy.

  • Among 1,641 patients, five-year recurrence-free rates were nearly identical between treatment groups at 91.8% without radiation and 92.7% with radiation (HR=0.88, p=0.51).

  • The findings suggest pathologic complete response in axillary nodes serves as a biomarker identifying patients who derive no benefit from additional regional radiation therapy.

The landmark NRG-NSABP B-51/RTOG 1304 clinical trial has delivered paradigm-shifting results that challenge conventional breast cancer treatment approaches, demonstrating that regional nodal irradiation (RNI) provides no benefit for patients whose axillary lymph nodes convert from positive to negative status following neoadjuvant chemotherapy. The findings, published in the New England Journal of Medicine, represent a significant departure from traditional radiation therapy protocols.

Study Design and Patient Population

The multi-institutional trial enrolled 1,641 women who initially presented with pathologically involved axillary nodes but achieved nodal pathologic complete response (pCR) after neoadjuvant chemotherapy. Patients were randomized post-surgery to receive either RNI or no additional nodal radiation, with meticulous stratification based on surgery type (mastectomy versus lumpectomy), hormone receptor status including estrogen (ER) and progesterone (PgR), HER2 receptor expression, use of adjuvant chemotherapy, and achievement of pCR within the breast tissue.
The trial design ensured contemporary standard-of-care treatments were uniformly administered, with mandatory anti-HER2 therapy for HER2-positive tumors and endocrine therapy for hormone receptor-positive tumors. The primary efficacy endpoint was invasive breast cancer recurrence-free interval (IBCRFI), encompassing both local and distant disease events.

Key Clinical Outcomes

The trial was designed for final analysis after either 172 IBCRFI events or ten years of follow-up. At the time-driven analysis, 109 events had been confirmed, representing 63% of the targeted event number. The results definitively showed that RNI did not significantly reduce invasive breast cancer recurrence, with a hazard ratio of 0.88 (95% confidence interval 0.60-1.28, p=0.51).
Five-year estimated IBCRFI rates were nearly identical between treatment arms—91.8% without RNI and 92.7% with RNI. Secondary outcomes including loco-regional recurrence-free interval, distant recurrence-free interval, overall disease-free survival, and overall survival likewise showed no improvement attributable to RNI.

Clinical Implications and Expert Perspective

Dr. Eleftherios Mamounas, the study's lead author from AdventHealth Cancer Institute, emphasized the clinical significance of these findings. "Although numerous prior clinical trials have demonstrated benefit from RNI in patients with positive axillary lymph nodes who undergo surgery first, this trial evaluated RNI in patients who presented with node-positive breast cancer but whose axillary lymph nodes converted to pathologically negative after neoadjuvant chemotherapy," Mamounas stated.
He noted that the study results demonstrate that pathologic complete response in axillary lymph nodes predicts no benefit from RNI, contrasting with historical data showing RNI benefits in patients with residual nodal disease or node-positive status upfront.

Mechanistic Understanding

The lack of benefit with RNI in this context likely relates to effective systemic eradication of micrometastatic disease by neoadjuvant chemotherapy, coupled with pathologic clearance of nodal tumor deposits. These events substantially reduce the tumor cell reservoir that regional radiotherapy aims to eliminate, creating therapeutic redundancy that suggests radiation-associated toxicities may be avoidable in these patients without undermining oncologic control.

Impact on Treatment Paradigms

These insights will likely recalibrate clinical guidelines, promoting more personalized radiation strategies. The findings emphasize that pathologic complete response in axillary nodes after neoadjuvant chemotherapy may serve as a robust biomarker identifying patients who derive little to no benefit from additional regional nodal radiation.
The trial's robust design incorporating both mastectomy and breast-conserving surgery patients, a wide spectrum of molecular subtypes, and standard adjunct systemic therapies ensures the findings are applicable to a broad breast cancer population in routine clinical care. The large sample size and meticulous stratification reinforce the validity and precision of the results.
This investigation was supported by multiple funding sources, including grants from the National Cancer Institute (NCI) and the Susan G. Komen Foundation, reflecting the collaborative commitment to advancing breast cancer treatment through rigorous clinical trials conducted by NRG Oncology, a leading research consortium dedicated to practice-changing investigations in cancer care.
Subscribe Icon

Stay Updated with Our Daily Newsletter

Get the latest pharmaceutical insights, research highlights, and industry updates delivered to your inbox every day.

© Copyright 2025. All Rights Reserved by MedPath