OncoMatch/Clinical Trials/NCT07227233
Artificial Intelligence and Machine Learning to Guide CDK4/6 Inhibitor Rechallenge in Breast Cancer.
Is NCT07227233 recruiting? Yes, currently enrolling (May 2026). This Phase 2 trial studies multiple treatments including A CDK4/6 inhibitor different from the first that the participant had received, plus fulvestrant. and Treatment of physician's choice for breast cancer.
Treatment: A CDK4/6 inhibitor different from the first that the participant had received, plus fulvestrant. · Treatment of physician's choice — The goal of this clinical trial is to learn if an artificial intelligence model will be able to select patients with advanced breast cancer who may respond to a second cyclin-dependent kinase 4/6 (CDK4/6) inhibitor after they have progressed on the first CDK4/6 inhibitor. Patients for this study need to have hormone receptor positive (HR+) human epidermal growth factor receptor 2 negative (HER2-) advanced breast cancer. The main questions the study aims to answer are: If the artificial intelligence model says that a patient's tumor should respond to the second CDK4/6 inhibitor, and that patient receives the second CDK4/6 inhibitor together with fulvestrant (an endocrine therapy also called Faslodex), will it take longer for the tumor to get worse than if the patient receives another type of therapy? Will the tumor respond better? Will the therapy be safe? Researchers will compare the combination of a second CDK4/6 inhibitor plus fulvestrant to the therapy chosen by the physician. Participants will: Take the assigned therapy based on the way the therapy is usually prescribed. Visit the clinic once every month for checkups, tests, and questionnaires. Keep a diary of the pills they take at home.
Check if I qualifyExtracted eligibility criteria
Cancer type
Breast Carcinoma
Biomarker criteria
Required: ESR1 hormone receptor positive
hormone receptor positive (HR+) ... per American Society of Clinical Oncology/College of American Pathologists (CAP) guidelines
Required: HER2 (ERBB2) negative
human epidermal growth factor receptor 2 negative (HER2-) ... per American Society of Clinical Oncology/College of American Pathologists (CAP) guidelines
Disease stage
Metastatic disease required
Performance status
ECOG 0–2(Ambulatory, capable of self-care)
Prior therapy
Must have received: cdk4/6 inhibitor — metastatic or adjuvant
Lab requirements
Blood counts
leukocytes > 3,000/microliter; hemoglobin > 8 g/deciliter; absolute neutrophil count > 1,200/microliter; platelets > 75,000/microliter
Structured fields extracted by AI. May contain errors — verify against the official protocol.
US trial sites
- University of California, San Diego · La Jolla, California
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