Final analysis of the NEOMET trial of neoadjuvant metformin: Examining effects on Ki67, gene expression, and pathway analysis in primary operable breast cancer.

Authors

Alastair Thompson

A. M. Thompson

University of Dundee, Dundee, United Kingdom

A. M. Thompson , T. Iwamoto , L. Jordan , C. Purdie , S. E. Bray , L. Baker , G. Hardie , L. Pusztai , S. L. Moulder , J. A. Dewar , S. M. Hadad

Organizations

University of Dundee, Dundee, United Kingdom, University of Texas M. D. Anderson Cancer Center, Houston, TX, Department of Investigational Cancer Therapeutics (Phase I Program), University of Texas M. D. Anderson Cancer Center, Houston, TX

Research Funding

Other

Background: Metformin is associated with a reduced incidence of breast cancer and enhanced response to neoadjuvant chemotherapy in epidemiological studies of diabetic women. Cell line and xenograft studies suggest metformin, widely used in the treatment of diabetes, may be a candidate anti-cancer agent. This randomized phase II neoadjuvant trial examined the effects of metformin on Ki67 and gene expression in primary breast cancer, testing the hypothesis that metformin has anti-cancer effects in women with breast cancer. Methods: Non-diabetic women with operable, primary invasive breast cancer received pre-operative metformin. The trial had two components: a pilot cohort of 8 luminal A patients had core biopsy at three time points: at presentation; a week later without treatment (internal control); then following metformin 500mg o.d. for one week increased to 1g b.d. for a further week up to definitive surgery. A further 47 Luminal A and Luminal B patients had core biopsy measurement at diagnosis, were randomized to metformin or no metformin, and 2 weeks later had core biopsy prior to resection. Ki67 measurements and transcriptome analyses were performed on formalin fixed paraffin embedded tissues. Results: The mean percentage of cells staining for Ki67 fell significantly in both the pilot cohort (p=0.041, paired t-test) and patients randomized to metformin (p=0.027, Wilcoxon rank test) following metformin treatment, but was unchanged in the control arm. By Ingenuity Pathway Analysis, the TNFR1 signaling pathway was most significantly affected by metformin: TGFB, MEKK were commonly up regulated and cdc42 down regulated. The mTOR and AMPK pathways were also significantly affected. By Gene Set Analysis the p53, BRCA1 and cell cycle pathways had reduced expressed following metformin. Conclusions: This window of opportunity trial presents evidence of antiproliferative and anti-cancer effects via specific biomarker pathways for metformin action in primary breast cancer and provides support for further trials testing the use of metformin in the treatment of breast cancer.

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Abstract Details

Meeting

2011 ASCO Annual Meeting

Session Type

Poster Discussion Session

Session Title

Breast Cancer - HER2/ER

Track

Breast Cancer

Sub Track

ER+

Citation

J Clin Oncol 29: 2011 (suppl; abstr 534)

Abstract #

534

Poster Bd #

23

Abstract Disclosures