RecruitingNot ApplicableNCT05977036

BettER: Biomarker Driven Early Therapeutic Selection in Patients With HR+ HER2- Metastatic or Unresectable Breast Cancer


Sponsor

Washington University School of Medicine

Enrollment

65 participants

Start Date

Sep 25, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

This is a prospective study to assess the impact of biomarker driven, early therapeutic switching and delayed imaging with the incorporation of DiviTum® serum TK1 activity ("DiviTum® TKa") in patients with HR positive, HER-2 negative metastatic or unresectable breast cancer. Patients will receive first-line treatment with a CDK4/6 inhibitor (CDK4/6i) and endocrine therapy. All patients will have blood drawn for thymidine kinase activity (TKa) testing at baseline and at C1D15. Patients who are found to have a lack of TKa suppression at C1D15 will be recommended to switch to an alternative therapy. Patients with suppressed C1D15 TKa levels will continue on CDK4/6i and endocrine therapy until clinical progression. Patients with TKa which remains suppressed will be recommended to delay restaging scans from 24 weeks to 36 weeks. The investigators hypothesize that a patient's TKa level at C1D15 is prognostic for progression-free survival (PFS) on a CDK4/6 inhibitor and early therapeutic switching in patients with a lack of C1D15 TKa suppression will be associated with prolonged PFS.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study is collecting biological samples (blood and sometimes tumor tissue) from patients with hormone receptor-positive, HER2-negative metastatic breast cancer to find biomarkers — biological signals — that predict how well they'll respond to standard first-line treatment (endocrine therapy plus a CDK4/6 inhibitor like ribociclib). **You may be eligible if...** - You have metastatic or advanced breast cancer that is hormone receptor-positive (HR+) and HER2-negative - You are about to start first-line standard treatment with hormone therapy plus a CDK4/6 inhibitor - You have had any prior treatment for earlier-stage breast cancer (including prior CDK4/6 inhibitor therapy completed more than 1 year ago) **You may NOT be eligible if...** - You have already started treatment for your metastatic disease - You are unable to provide the required biomarker samples Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DEVICEDiviTum® TKa assay

Will be utilized for determination of serum enzymatic activity of TK1 according to the manufacturer's instructions

DRUGCDK4/6 + Endocrine therapy

FDA-approved endocrine therapy plus CDK4/6 inhibitor. Ribociclib is the preferred CDK4/6 inhibitor. In the event this drug cannot be obtained due to insurance authorization or if there are specific side effect profile concerns from the treating physician, an alternative CDK4/6 inhibitor is allowed.


Locations(1)

Washington University School of Medicine

St Louis, Missouri, United States

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NCT05977036


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