A Pilot Study of Monitoring Insulin Levels and Treating Hyperinsulinemia and Hyperglycemia With Pioglitazone in Patients Treated With Alpelisib for Metastatic Breast Cancer.

Trial statusRecruiting
Trial phaseEarly Phase 1
Trial typeInterventional
Biological sexFemale
Age18-85
SponsorRambam Health Care Campus

About this trial

The goal of this study is to test whether monitoring insulin levels and using pioglitazone to treat hyperglycemia and hyperinsulinemia in patients treated with Alpelisib for metastatic breast cancer is feasible and safe, and to assess the rates of glycemic control, dose reductions and treatment discontinuation and the progression free survival of patients treated with this regimen.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Patients with ER positive HER2 negative metastatic breast cancer, harboring an activating PIK3CA mutation, scheduled to start treatment with Alpelisib and fulvestrant.

Ages 18 - 85

ECOG performance status 0, 1 or 2

Ability to understand and willingness to sign a written informed consent.

Disqualifiers

Impairment of gastrointestinal (GI) function or GI disease that may significantly alter the absorption of Alpelisib

Uncontrolled diabetes mellitus, defined as HbA1c above 8%

Diabetes mellitus controlled by insulin

Uncontrolled intercurrent illness including, but not limited to: active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements

Trial design

Design model

Single group

Treatments tested in this trial

  • Pioglitazone

    Drug

    hyperinsulinemia and hyperglycemia

Treatment groups

30 Participants
are divided into 1 treatment group
Group A: Treatment armExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Rate of severe (grade 3 and 4) hyperglycemia in patients enrolled in the study and in patients treated per protocol

Time frame
through study completion, an average of 1 year
2

Rate of all grade hyperglycemia in patients enrolled in the study and in patients treated per protocol

Time frame
through study completion, an average of 1 year
3

Progression free survival in patients enrolled in the study and in patients treated per protocol

Time frame
through study completion, an average of 1 year

Secondary outcomes

Other outcomes

Sponsors and contacts

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