Preoperative Window Study of Metformin for the Treatment of Endometrial Cancer

UNC Lineberger Comprehensive Cancer Center

Status and phase

Completed

Early Phase 1

Conditions

Endometrial Cancer

Treatments

Drug: Metformin

Study type

Interventional

Funder types

Other

NIH

Identifiers

NCT01911247

LCCC1102

1K23CA143154-01A1 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

The overall goal of this proposal is to investigate the potential benefit of metformin as a novel therapy for the treatment of endometrial cancer. Investigators will evaluate the effect of short-term metformin treatment on the endometrium of obese women with endometrial cancer by comparing each patient's endometrial biopsy before treatment with metformin to their post-treatment hysterectomy specimen.

Participants: Obese women who are to undergo surgical staging for endometrial cancer will also receive short-term treatment (1-4 weeks) with metformin that will continue until the day prior to surgical staging.

The effect of metformin on proliferation, apoptosis and downstream signaling pathways will be compared between pre-treatment endometrial biopsies and post-treatment hysterectomy specimens. Tissue microarrays will be constructed and immunohistochemstry performed to evaluate proliferation, apoptosis and changes in critical signaling pathways mediated by metformin, and these findings will be correlated with our in vitro preclinical studies. Fresh tissue will also be obtained, and Western immunoblotting will be used to assess expression of the phosphorylated forms of the downstream targets of metformin. The hypothesis is that treatment with metformin will result in a decrease in proliferative markers and an increase in markers of apoptosis in the endometrial cancer tumors. AMPK phosphorylation and inhibition of critical downstream targets of the mTOR pathway will be seen in the post-treatment hysterectomy specimens. Metabolomic profiling will also be performed of tumors and associated biofluids (i.e. serum and urine) before and after treatment with metformin to identify potential biomarkers of response to this therapy.

Enrollment

28 patients

Sex

Female

Ages

18 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Be between the ages of 18-75 years old
Have a confirmed diagnosis of type I endometrial cancer (endometrioid) based on pre-operative endometrial biopsy or dilation and curettage (D&C)
Be obese (BMI greater than or equal to 30) with or without diabetes
Have no contraindications to short-term metformin therapy
Have a serum creatinine greater 1.0 mg/dL
Have normal serum transaminase values (AST and ALT)
Need to be able to undergo metformin treatment for a minimum of 1 weeks but no more than a maximum of 4 weeks prior to surgical staging

Exclusion criteria

Are currently taking metformin or have taken metformin in the past 6 months or have a history of an allergic reaction or intolerance at any time to metformin
Have a history of liver or renal dysfunction
Have a history of alcoholism
Have a history of vitamin B12 deficiency
Are pregnant
Are currently taking insulin
Are currently taking any hormonal therapy or have been on hormonal therapy in the past 4 weeks
Are taking a drug that may significantly interact or influence the metabolism of metformin
In the opinion of the investigator, the patient is felt not to be appropriate for the study