Clinical Trials Directory

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

TypeNameDescription
RADIATIONWhole breast irradiationRadiotherapy to the whole breast alone.
RADIATIONWhole breast and nodal irradiationRadiotherapy 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.