drugset / Trial / NCT05826964

Levels of Circulating Tumor DNA as a Predictive Marker for Early Switch in Treatment for Patients With Metastatic (Stage IV) Breast Cancer

NCT05826964

Phase 2 Active not recruiting 24 enrolled University of Miami
RandomizedSequentialOpen-labelTreatment

Summary

The majority of patients (pts) with breast cancer have hormone receptor positive (HR+) disease, and this holds true for pts with advanced breast cancer (ABC). Currently frontline therapy for pts with HR+ ABC is antihormonal therapy with an aromatase inhibitor or selective estrogen receptor degrader plus a CDK4/6i. The proposed trial is a randomized study to further evaluate the potential benefit of switching a frontline regimen at the time that a molecular signal, ctDNA, suggests progression prior to detection of clinical progression using standard methods. The purpose of this study is to determine whether switching treatment earlier in the disease process, based on molecular progression, will increase the amount of time that a patient's metastatic breast cancer is controlled compared to patients with metastatic breast cancer who receive treatment later based on diagnostic imaging results or other methods currently used in medical practice.

Timeline

Start
2023-06-12
Primary completion
2026-07-31
Completion
2029-07-31

Drugs

EvaluationDrugModalityDoseRoute
Subject Abemaciclib Small molecule
Subject Alpelisib Small molecule
Subject Anastrozole Other / unclassified
Subject Capecitabine Small molecule
Subject Elacestrant Other / unclassified
Subject Eribulin Small molecule
Subject Everolimus Small molecule
Subject Exemestane Small molecule
Subject Fulvestrant Small molecule
Subject Letrozole Other / unclassified
Subject Olaparib Small molecule
Subject Palbociclib Small molecule
Subject Ribociclib Small molecule
Subject Talazoparib Small molecule
Subject Tamoxifen Small molecule
Subject Triciribine Unknown
Subject Vinorelbine Small molecule