Breast Cancer Clinical Trial

Preventing High Blood Sugar in People Being Treated for Metastatic Breast Cancer

Summary

The purpose of this study to find out whether a very low carbohydrate diet (ketogenic diet), a low carbohydrate diet, or the study drug canagliflozin can prevent high blood sugar and may improve the effectiveness of cancer therapy in people who are receiving standard treatment with alpelisib and fulvestrant for their metastatic PIK3CA-mutant breast cancer.

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

Histologically confirmed metastatic HR-positive, HER2-negative breast cancer. HR positive is defined by ER status >10% immunohistochemical (IHC) staining of any intensity. HER2 negativity is defined as the following as per the 2018 American Society of

Clinical Oncology and College of American Pathologists guidelines:

IHC score of 0 or 1+ or
Single-probe average HER2 copy number of <4 signals/cell or
Dual-probe HER2/CEP17 ratio <2 with an average HER2 copy number of <4 signals/cell or
IHC 0, 1+, or 2+ and dual-probe HER2/CEP17 ratio ≥2 with an average HER2 copy number of <4 signals/cell or
IHC 0 or 1+ and dual-probe HER2/CEP17 ratio <2 with an average HER2 copy number of ≥6 signals/cell or

IHC 0 or 1+ and dual-probe HER2/CEP17 ratio <2 with an average HER2 copy number of ≥4 and <6 signals/cell.

Presence of one or more activating PIK3CA mutations in tumor tissue.
Measurable or non-measurable disease per RECIST v1.1 OR at least one predominantly lytic bone lesion must be present.
Written informed consent provided
Female or male ≥18 years of age
Adequate archived tumor tissue for the analysis of PIK3CA mutational status or evaluable circulating tumor DNA (ctDNA) for analysis of PIK3CA mutation status
Recurrence or progression of disease during or after endocrine-based therapy
Eastern Cooperative Oncology Group performance status of 0 or 1.
Life expectancy ≥6 months.
Adequate organ and marrow function as defined below:
Hemoglobin ≥9.0 g/dL (without blood transfusion within 7 days of laboratory test used to determine eligibility)
Absolute neutrophil count ≥1.5 × 109/L (without granulocyte colony stimulating factor support within 2 weeks of laboratory test used to determine eligibility)
Platelet count ≥100 × 109/L (without transfusion within 2 weeks of laboratory test used to determine eligibility)
Total bilirubin (TB) ≤1.0 × institutional upper limit of normal (ULN; Patients with known Gilbert's disease who have TB ≤3 × ULN may be enrolled)
Aspartate transaminase/alanine transaminase ≤2.5 × ULN with normal alkaline phosphatase (≤5 × ULN for patients with liver metastases) OR ≤1.5 × ULN in conjunction with alkaline phosphatase >2.5 × ULN

Creatinine ≤1.5 mg/dL.

Fasting blood glucose ≤140 mg/dL and HbA1c <8% (both criteria have to be met) and not on anti-hyperglycemic medications other than metformin (i.e., metformin is allowable if fasting blood glucose and HbA1c parameters are met).
Able to swallow oral medication.
Willing to be randomized to any of the diet arms and able to comply with the protocol for the duration of the study including undergoing treatment and scheduled visits and examinations
Women must be of postmenopausal status. Postmenopausal status is defined by any one of the following criteria:
Prior bilateral oophorectomy or current ovarian suppression with a GnRH agonist
Age ≥60 years
Age <60 years and amenorrheic for at least 12 months (spontaneous cessation of menses for 12 consecutive months or more in the absence of chemotherapy

Exclusion Criteria:

Multiple prior lines of chemotherapy in the metastatic setting (One line of chemotherapy is allowed. Also prior treatment with CDK4/6 inhibitors is allowed)
Currently participating in a study of an investigational agent
Current participation in a formalized weight loss program or currently consuming a ketogenic diet
Body mass index < 20 kg/m^2
Known hypersensitivity to alpelisib, fulvestrant, canagliflozin, or to any of the excipients of alpelisib or fulvestrant.
Concurrent malignancy (basal cell carcinoma of the skin, squamous cell carcinoma of the skin, or cervical cancer in situ that have undergone curative intent therapy are allowed)
Type 1 diabetes mellitus
Uncontrolled type 2 diabetes mellitus (hemoglobin A1c ≥8.0)
Type 2 diabetes mellitus requiring treatment with a sulfonylurea, meglitinide, SGLT2 inhibitors or insulin.
Vegetarian or vegan eating habits.
Allergy or intolerance to egg, gluten, nut or milk protein that would interfere with adherence to diet.
Individuals with impaired decision making capacity

Study is for people with:

Breast Cancer

Phase:

Phase 2

Estimated Enrollment:

106

Study ID:

NCT05090358

Recruitment Status:

Recruiting

Sponsor:

Memorial Sloan Kettering Cancer Center

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There are 8 Locations for this study

See Locations Near You

Memorial Sloan Kettering Basking Ridge (Limited Protocol Activities)
Basking Ridge New Jersey, 07920, United States More Info
Neil Iyengar, MD
Contact
646-888-8103
Memorial Sloan Kettering Monmouth (Limited Protocol Activities)
Middletown New Jersey, 07748, United States More Info
Neil Iyengar, MD
Contact
646-888-4714
Memorial Sloan Kettering Bergen (Limited Protocol Activities)
Montvale New Jersey, 07645, United States More Info
Neil Iyengar, MD
Contact
646-888-4714
Memorial Sloan Kettering Suffolk - Commack (Limited protocol activity)
Commack New York, 11725, United States More Info
Neil Iyengar, MD
Contact
646-888-4714
Memorial Sloan Kettering Westchester (All protocol Activities)
Harrison New York, 10604, United States More Info
Neil Iyengar, MD
Contact
646-888-4714
Memorial Sloan Kettering Cancer Center
New York New York, 10065, United States More Info
Neil Iyengar, MD
Contact
646-888-4714
Weill Cornell Medical College (Data Collection & Data Analysis)
New York New York, 10065, United States More Info
Eleni Andreopoulou, MD
Contact
646-962-9888
Memorial Sloan Kettering Nassau (Limited Protocol Activities)
Uniondale New York, 11553, United States More Info
Neil Iyengar, MD
Contact
646-888-4714
Ohio State University (Data Collection & Data Analysis)
Columbus Ohio, 43210, United States More Info
Sagar Sardesai, MD
Contact
614-293-8000

How clear is this clinincal trial information?

Study is for people with:

Breast Cancer

Phase:

Phase 2

Estimated Enrollment:

106

Study ID:

NCT05090358

Recruitment Status:

Recruiting

Sponsor:


Memorial Sloan Kettering Cancer Center

How clear is this clinincal trial information?

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