Clinical Trial

Postoperative Radiotherapy in Breast Cancer- Concurrent or Sequential With Chemotherapy

Study acronym: CONCERT
Recruiting Phase 3
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Summary
This clinical research aims to determine if concurrent chemotherapy and radiation therapy is more effective than sequential chemotherapy and radiation therapy for patients with stage IIB-III breast cancer. It seeks to answer the following key questions: 1. When compared to sequential treatment, does concurrent chemoradiotherapy increase disease-free survival? 2. What effects does concurrent treatment have on post-operative look, quality of life, and side effects including arm swelling (lymphoedema)? 3. What are each treatment approach's financial costs? Researchers will compare the following to groups: Arm A: Participants in the sequential treatment group will first undergo chemotherapy and then radiation. and Arm B: Participants in the concurrent treatment group will undergo radiation therapy while undergoing chemotherapy. Participants are going to: 1. Get the usual chemotherapy (taxanes and/or anthracyclines). 2. Receive radiation therapy for three to four weeks. 3. Have follow-up visits every 6months for 5years to check for cancer recurrence, side effects, and quality of life.
Trial Details
NCT Number NCT06926543
Lead Sponsor Dr. Tabassum Wadasadawala
Conditions Invasive Breast Cancer, Stage III Breast Cancer, Stage IIB Breast Cancer
Enrollment 858 participants
Start Date 2024-05-14
Primary Completion 2031-05 (estimated)
Study Completion 2031-05 (estimated)
Updated on ClinicalTrials.gov 2025-04-13