Time Restricted Eating And Metformin (TEAM) in Invasive Breast Cancer (IBC) or Ductal Carcinoma in Situ (DCIS). A Randomized, Phase IIb, Window of Opportunity Presurgical Trial.

Who is this study for? Patients with invasive breast cancer or ductal carcinoma in situ
What treatments are being studied? Metformin Hydrochloride+Monitoring+Nutritional Assessment+Short-Term Fasting
Status: Recruiting
Location: See all (3) locations...
Intervention Type: Other, Procedure, Drug
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

This phase IIb trial studies the combined effect of prolonged nightly fasting and metformin hydrochloride extended release in decreasing breast tumor cell proliferation and other biomarkers of breast cancer. Preventing invasive breast cancer or DCIS. Metformin is widely used to treat type II diabetes and is associated with a decreased risk of cancer and death in diabetic individuals. Intermittent fasting may protect cancer patients from the toxic effects of chemotherapy agents without causing chronic weight loss. The combination of intermittent fasting and metformin may reduce breast cancer growth and may be used in women at risk for breast cancer or other cancers associated with being overweight.

Eligibility
Participation Requirements
Sex: Female
Minimum Age: 18
Healthy Volunteers: f
View:

• Women with histologically confirmed luminal (ER+ve and/or progesterone \[PgR\]+ve \>= 1%) operable IBC (cT1-2, cN0-1, Mx) candidate to elective surgery and not to neo-adjuvant treatment. Women with larger tumors who refuse neo-adjuvant chemotherapy before surgery can also be eligible. Luminal HER2+ve (cT1, cN0) IBC and DCIS are also eligible

• Age \>= 18 years

• Eastern Cooperative Oncology Group (ECOG) performance status =\< 1 (Karnofsky \>= 70%)

• Leukocytes \>= 3,000/microliter

• Absolute neutrophil count \>= 1,500/microliter

• Platelets \>= 100,000/microliter

• Aspartate aminotransferase (AST) (serum glutamic-oxaloacetic transaminase \[SGOT\])/alanine aminotransferase (ALT) (serum glutamate pyruvate transaminase \[SGPT\]) =\< 1.5 x institutional upper limit of normal

• Creatinine within normal institutional limits

• Creatinine clearance estimated with Cockcroft-Gault formula \> 45 mL/min

• Female participants of child-bearing potential must agree to use contraception such as barrier method of birth control or abstinence, prior to study entry and for the duration of study participation. Should a woman become pregnant or suspect she is pregnant while participating in this study, she has to inform her study physician immediately. The effects of metformin hydrochloride extended release on the developing human fetus at the recommended therapeutic dose are unknown

• Ability to understand and the willingness to sign a written informed consent document

Locations
United States
Texas
M D Anderson Cancer Center
RECRUITING
Houston
Other Locations
Italy
Galliera Hospital
RECRUITING
Genoa
European Institute of Oncology
RECRUITING
Milan
Contact Information
Primary
Parijatham Thomas, MD
psthomas@mdanderson.org
713-745-1075
Time Frame
Start Date: 2023-04-04
Estimated Completion Date: 2025-11-20
Participants
Target number of participants: 120
Treatments
Experimental: Arm I (fasting, glucose monitoring, counseling, metformin)
Patients fast for \>= 16 hours every night and use the continuous glucose monitoring system for 4-6 weeks. Patients also receive nutritional counseling sessions on days 0 and 10. Beginning week 2, patients also receive metformin hydrochloride extended release PO QD until the day of surgery. Treatment continues for 4-6 weeks (until surgery) in the absence of disease progression or unacceptable toxicity. Patients undergo the collection of blood samples at baseline and at the final study visit (days 28-43), and the collection of tissue at the time of surgery (days 28-43).
Active_comparator: Arm II (glucose monitoring)
Patients continue their usual dietary pattern and use the continuous glucose monitoring system for 4-6 weeks (until surgery). Patients undergo the collection of blood samples at baseline and at the final study visit (days 28-43), and the collection of tissue at the time of surgery (days 28-43).
Related Therapeutic Areas
Sponsors
Leads: M.D. Anderson Cancer Center
Collaborators: National Cancer Institute (NCI)

This content was sourced from clinicaltrials.gov