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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.

Phase 2RecruitingUniversity of California, San DiegoNCT07227233Data as of May 2026

Treatment: A CDK4/6 inhibitor different from the first that the participant had received, plus fulvestrant. · Treatment of physician's choiceThe 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.

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Extracted 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

Max 1 prior line
Min 1 prior line

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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