Trials / Active Not Recruiting
Active Not RecruitingNCT03269981
Randomized Study of Elective Regional Lymph Node Irradiation in N1 Breast Cancer
A Phase III Prospective Randomized Study of Elective Regional Lymph Node Irradiation in Pathologic N1 Breast Cancer Patients Treated With Breast Conserving Surgery
- Status
- Active Not Recruiting
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 827 (actual)
- Sponsor
- Samsung Medical Center · Academic / Other
- Sex
- Female
- Age
- 20 Years – 70 Years
- Healthy volunteers
- Not accepted
Summary
This study evaluates the impact of elective regional lymph node irradiation on N1 breast cancer patients receiving post-lumpectomy radiotherapy and anthracycline plus taxane (AT)-based chemotherapy. We randomly assign patients having one to three metastatic lymph nodes (pN1) after breast-conserving surgery (BCS) and AT-based chemotherapy to undergo either whole-breast and regional nodal irradiation (WB+RNI group) or whole-breast irradiation alone (WBI group).
Detailed description
Objective: * Compare the effect of post-BCS WBI vs. WB+RNI on disease-free survival in pN1 breast cancer patients who received AT-based chemotherapy. * Evaluate the impact of WBI or WB+RNI according to molecular subtype of tumor. * Compare the treatment-related toxicities between the WBI and WB+RNI. * Compare the patient's quality of life between the WBI and WB+RNI. Outline: This is a a randomized, multi-center, phase III study. Patients are stratified according to molecular subtype of tumor (luminal A vs luminal vs luminal HER2 vs HER2-enriched vs basal-like), axillary lymph node management (sentinel lymph node biopsy \[SLN\] only vs axillary lymph node dissection+/- SLN) and participating institutions. Patients are randomized to one of two treatment arms. * Arm I: Patients receive WB+RNI. * Arm II: Patients receive WBI alone. Arm circumference and quality of life (EORTC QLQ-C30 \& EORTC QLQ-BR23) are assessed within 2 weeks prior to randomization, during the last week of radiotherapy, at 3 months after completion of radiotherapy, and then annually thereafter for five years. Patients are followed at 3 months after completion of radiotherapy and annually thereafter for seven years.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| RADIATION | Whole breast irradiation | Radiotherapy to the whole breast alone. |
| RADIATION | Whole breast and nodal irradiation | Radiotherapy to the whole breast and regional lymph nodes. |
Timeline
- Start date
- 2017-04-01
- Primary completion
- 2029-12-30
- Completion
- 2029-12-30
- First posted
- 2017-09-01
- Last updated
- 2023-11-27
Locations
1 site across 1 country: South Korea
Source: ClinicalTrials.gov record NCT03269981. Inclusion in this directory is not an endorsement.