Neoplasms

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Nutritional and Metabolic Diseases

Breast Neoplasms

Insulin Resistance

Breast Diseases

Skin Diseases

Hyperinsulinism

Metabolic Diseases

Glucose Metabolism Disorders

Hypoglycemic Agents

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Metformin

White women on metformin Extended release 750 mg BID

Black women on metformin Extended release 750 mg BID

initial dose of metformin of 750 mg Q.D. (with dinner) for 3-4 weeks. They then will be increased to the final dose of 750 mg BID (breakfast and dinner) until the end of the study.

Metformin Extended Release Oral Tablet

Ericka Seidemann, MA

Cynthia Harper-Weinstein

Breast cancer is one of the most common malignancies in women globally, with \~1.4 million new cases diagnosed annually Breast cancer is one of the leading causes of cancer-related morbidity and mortality among women worldwide. While diabetes/insulin-resistance and breast cancer are distinct diseases, insulin-signaling plays a central role in both illnesses. Insulin activates key cancer processes including epithelial-mesenchymal transition (EMT), tissue inﬂammation, motility, and angiogenesis. There are key opportunities to impact and prevent hyperinsulinemia during breast cancer prevention, surgical assessment, and chemotherapy. Given the high prevalence of undiagnosed pre-diabetes and diabetes in the United States and worldwide, preoperative screening to identify such patients prior to surgical intervention is warranted. While it is not standard of care to test for insulin-resistance during the course of breast cancer screening and treatment, it is standard of care to screen and test high risk women for insulin-resistance as part of whole woman care. Given the important role insulin signaling plays in driving signaling pathways that promote aggressive cancer biology, more attention should be paid by cancer physicians to screening and treating insulin resistance. Several studies have reinforced a link between breast cancer risk and diabetes. Moreover, metformin significantly reduces breast cancer risk, compared to patients who are not using metformin and is independent of diabetes status. As metformin has an association with decreased breast cancer recurrence, as well as potentially improved survival, disparities in insulin resistance between black and white women with breast cancer is important to investigate. It is hypothesized that metformin decreases the development of resistance in breast cancer cells, thereby allowing current chemotherapy agents to work synergistically with metformin. Our objective is to elucidate whether or not metformin is efficacious in improving insulin resistance in black and white women with breast cancer and if racial disparities in breast cancer prognosis can be partially explained by differences in pre-diagnosis insulin resistance which are improved with metformin therapy.

Even as cancer research has led to more advanced, targeted cancer treatments than ever before, not all patients are able to reap the benefits of these efforts, as demonstrated by their persistently worse survival outcomes, lack of accrual onto clinical trials, and lower rates of genetic testing. According to the American Cancer Society, black patients have the highest death rates and shortest duration of survival of any racial or ethnic group in the U.S. for most cancers. Black individuals with cancer are 25% more likely to die of their disease than white patients. Although persisting across tumor types, this disparity is particularly evident among black women, whose population-based breast cancer mortality rate is higher than white women. Compared with white women, black women have a 42% higher breast cancer mortality rate and twofold higher incidence of biologically aggressive triple-negative disease. Additionally, the American Cancer Society reported that black women are significantly more likely to die of breast cancer than white women, a disparity that has increased over time.

For decades, researchers attributed higher mortality rates to socioeconomic factors such as inadequate health insurance, fewer years of education and lower income. However, research now supports the hypothesis that tumor biologic differences among black women could have a greater impact on response to treatment and outcomes. Some disparities are a function of environmental stressors influenced by race that affect biology. Body mass index (BMI), obesity, and rates of diabetes are higher for African Americans. Obesity is associated with a 35% to 40% increased risk of breast cancer recurrence and death and therefore poorer survival outcomes. This association is most clearly established for estrogen receptor-positive breast cancer, with the relationship in triple-negative and human epidermal growth factor receptor 2-overexpressing subtypes less well established. A range of biologic mechanisms that may underlie this association has been identified. In an early meta-analysis evaluating BMI and breast cancer risk, the authors found that every 5 kg/m2 increase of BMI was associated with 12% increased risk of breast cancer in postmenopausal women. The inflammatory and endocrine effects of obesity, a major risk factor for type 2 diabetes (T2DM), have been proposed as central mechanisms explaining associations between diabetes and cancer.

Approximately \~ 10% of all cancers in women are attributable at least in part to obesity, with certain tumor types exhibiting an even stronger relationship between excess weight and cancer risk. Among these are breast and colon cancer, in which obesity promotes tumor appearance, progression, and metastasis in rodent models and in human patients. Obesity is associated with elevated insulin levels and increased insulin resistance. Insulin, a member of a family of growth factors that includes insulin-like growth factor (IGF)-I and IGF-II, exerts mitogenic effects on normal and malignant breast epithelial cells, acting via insulin and IGF-I receptors. Insulin resistance could lead to compensatory hyperinsulinemia, which enhances the cross-binding of insulin to the insulin-like growth factor-1 (IGF-1) receptors expressed on breast epithelial cells. Moreover, hyperinsulinemia may also accelerate the pathogenesis of breast cancer by stimulation of hepatic IGF-1 synthesis and inhibition the hepatic expression of IGF-1 receptors, leading to an increased circulating IGF-1 level. Interfering with insulin signaling may slow tumor growth while activation of the insulin receptor may promote tumor progression.

Hyperinsulinemia, which occurs as a consequence of lipid-induced insulin resistance and may also hasten its progression, is one of many putative links that may explain the association between obesity and cancer. Insulin promotes tumor cell division in vitro and plasma insulin concentrations are independently correlated with an increased risk and accelerated progression of both breast and colon cancer. High levels of fasting insulin identify women with poor outcomes in whom more effective treatment strategies should be explored. Black women are twice as likely to have prediabetes and type 2 diabetes as white women; improved monitoring of blood sugar and insulin levels to identify women with prediabetes could provide opportunities for reduction of the incidence of ER-negative breast cancer. A 12-week to 18-week course of chemotherapy appears to statistically significantly increase metabolic syndrome (MetS) and related anthropometrics, biomarkers of glucose metabolism, and inflammation in patients with early-stage breast cancer with no preexisting MetS. Lifestyle interventions such as diet and exercise may be preventive approaches for use during chemotherapy to reduce the onset of MetS in patients with breast cancer.

Breast cancer (BC) is one of the most common malignancies occurring in females. Weight loss and lifestyle interventions, as well as metformin and other obesity-targeted therapies, are promising avenues that require further study in women with breast cancer. The oral insulin-sensitizing drug metformin is a first line therapeutic in the management of T2DM. Metformin is a biguanide agent that reduces hepatic glucose production, increases hepatic fatty acid oxidation, reduces inflammation, and improves peripheral insulin sensitivity These activities reduce circulating glucose and insulin levels, although the exact mechanisms by which metformin achieves these effects are not well understood. In prior clinical studies elevated insulin levels were associated with poorer outcomes in patients with breast cancer; the use of metformin in women with early-stage breast cancer has been shown to reduce insulin levels. Metformin may affect breast cancer proliferation depending on a woman's insulin resistance, with decreased proliferation occurring in women with an increased homeostasis model assessment index (more insulin resistant). The rate of pathologic complete response was three time higher in women receiving neoadjuvant treatment for early-stage breast cancer plus metformin than in those women receiving neoadjuvant therapy without metformin.. Metformin has also been shown to have antiproliferative activity in vitro against multiple cancer cells lines. An early meta-analysis performed on T2DM patients taking metformin with cancer reported a 31% reduction in the incidence of new cancers including pancreas, colorectal, breast, and lung. Recent meta-analyses confirm that individuals with T2DM who also have lung, colorectal, and liver cancer derive significant survival benefits regarding clinical outcomes if also on metformin. Patients with breast cancer benefited from metformin treatment in terms of all cause survival (overall survival or chance of remaining alive after diagnosis). Data from previously conducted studies has shown metformin decreased the incidence of cancer and cancer-related deaths in patients with diabetes. Cellular glucose metabolism is linked tightly with the proliferation and development of breast cancer. Several studies suggested that metformin reduces the incidence of breast cancer in T2DM patients. Cancer cells show enhanced glucose uptake and metabolism and prefer glycolysis over OXPHOS, which is called the "Warburg effect." The noted specialty of metformin is to decrease glucose levels, thereby limiting the availability of energy for cancer cells. Metformin was also shown to decrease FAS expression, an essential component of the fatty acid synthesis pathway, thus affecting the survival of cancer cells. Metformin affects AMP-activated protein kinase, which effects mitochondrial energy generation and may deprive malignant, inefficient cells of energy and therefore reduce their potential growth rate. Although some of the observations \[with metformin\] imply not just \[preventing\] a progression of cancer but an incidence of cancer, which might suggest broader effects than merely energy deprivation. In parallel with that data, there are experimental findings that support a direct effect of metformin on specific pathways that mediate or promote cancer. It's been shown in both animal models and cell lines that metformin can inhibit some of the key steps that are important for tumors to grow, such as promotion of cell growth, motility, invasion, and migration. These findings provide us with new insight in the use of metformin combined with other drugs to treat tumors.

Epidemiologic studies suggest that metformin use may be associated with both reduced cancer incidence and mortality. In a study, Tesneg and colleagues analyzed data from 493,704 men and 502,139 women without colon cancer covered by national health insurance from 2003 to 2005, assessing whether metformin use had a protective effect. Although patients with diabetes had a higher risk for developing colon cancer, patients assigned metformin had a 27% reduced risk, according to researchers. Comparing patients with diabetes for less than 1 year, between 1 and 2 years, and at least 3 years with patients without diabetes, adjusted RRs were 1.308 (95% CI, 1.02-1.679), 1.087 (95% CI, 0.9-1.313) and 1.185 (95% CI, 1.055-1.33), respectively. The duration of metformin use showed an inverse trend, according to researchers, with an RR of 0.643 (95% CI, 0.49-0.845) in users for at least 3 years vs. nonusers. A few mechanisms have been hypothesized to explain what may be happening. The most prominent theory is the idea that metformin activates a specific protein kinase, which down regulates the mTOR signaling pathway, which is important for tumor cell metabolism. More broadly, there is some evidence that insulin itself - and insulin-related pathways - may promote cancers. There is the thought that metformin does modulate insulin and sensitizes cells to insulin, and that may also have something to do with its effects. Our objective is to elucidate whether or not metformin is efficacious in improving insulin resistance in black and white women with breast cancer and if racial disparities in breast cancer prognosis can be partially explained by differences in pre-diagnosis insulin resistance which are improved with metformin therapy.

Breast cancer tumor response rate to metformin treatment prior to surgery in black vs. white women.

Metformin Use to Reduce Disparities in Newly Diagnosed Breast Cancer

Metformin Use to Reduce Disparities in Newly Diagnosed Breast Cancer Response to Neoadjuvant Treatment

breast cancer response rate to metformin treatment prior to surgery pathologic response to treatment at surgery will be defined by the following categories: 0-no response; 1-partial response; and 2-complete response with metformin therapy

Mean blood glucose (MBG) concentrations will be calculated by summing glucose values obtained at 0, 30, 60, and 120 minutes during the OGTT and dividing by 4.

HOMA will be calculated using the equation: fasting insulin concentration (μIU/mL) × fasting glucose concentration (mmol/L) 22.5

SIOGTT will be calculated according to the formula:

10,000/√ \[fasting glucose (mg/dL) ×fasting insulin (μU/L) × \[MPG × MSI during OGTT\], where MPG (mg/dL) is mean plasma glucose OGTT, and MSI (μIU/mL) is mean serum insulin during OGTT

IGI/HOMA-IR estimated as the insulinogenic index (IGI) derived from the ratio of the increment of insulin to that of glucose 30 minutes after a glucose load (insulin 30 min - insulin 0 min/glucose 30 min - glucose 0 min) corrected for by the relative level of insulin resistance

IS-SI derived by applying the concept of the disposition index to measurements obtained during the 2-h OGTT and calculated as the index of insulin secretion factored by insulin resistance (ΔINS/ΔPG 30 x Matsuda SIOGTT) during the OGTT

Our Lady of the Lake Hospital

American Cancer Society, Inc.

Pfizer

Woman's

Digestive System Diseases

Symptoms and General Pathology

Ear, Nose, and Throat Diseases

Gastroesophageal Reflux

Barrett Esophagus

Metaplasia

Esophageal Motility Disorders

Esophageal Spasm, Diffuse

Deglutition Disorders

Esophageal Diseases

Gastrointestinal Diseases

Precancerous Conditions

Participants who self-identify as "not-Hispanic or Latino" and "White" and have been diagnosed by a physician with gastroesophageal reflux disease and do not have Barrett's esophagus.

Participants who self-identify as "not-Hispanic or Latino" and "African American" and have been diagnosed by a physician with gastroesophageal reflux disease and do no have Barrett's esophagus.

Participants who self-identify as "not-Hispanic or Latino" and "White" and have been diagnosed by a physician with Barrett's Esophagus.

Participants who self-identify as "not-Hispanic or Latino" and "African American" and have been diagnosed by a physician with Barrett's Esophagus.

Nicholas Shaheen, MD, MPH

Xiaoxin Chen, MD, PhD

The goal of the proposed research is to investigate the molecular mechanisms of racial disparity in Barrett's esophagus (BE), the premalignant lesion of esophageal adenocarcinoma. Specifically, the investigators hypothesize that environmental factors, genetic factors, and potentially gene environment interactions play crucial roles in the observed racial disparity in developing Barrett's esophagus.

Patients are recruited through UNC hospitals prior to scheduled esophagogastroduodenoscopy (EGD). Participants complete a questionnaire, have body measurements obtained, and have blood, biopsies, and gastric aspirate collected. Participants also complete a 24 hour pH impedance test.

The goal of the proposed research is to investigate the molecular mechanisms of racial disparity in Barrett's esophagus, the premalignant lesion of esophageal adenocarcinoma. Specifically, the investigators hypothesize that environmental factors, genetic factors, and potentially gene environment interactions play crucial roles in the observed racial disparity in developing Barrett's esophagus.

Participants: Patients aged 18-80 presenting at the Gastrointestinal (Gl) Endoscopy Clinic at UNC-Chapel Hill for elective upper endoscopy with a primary or secondary indication of reflux symptoms.

Procedures (methods): Endoscopic biopsy, pH impedance and sampling of gastric secretions will be performed according to our standard protocol. A series of questionnaires assessing demographics, environmental exposure (e.g., smoking, drinking), markers of socioeconomic status (SES), body measurement, previous health history, and gastroesophageal reflux disease (GERD) symptomatology will be administered to our subjects.

serum, plasma, buffy, esophageal biopsies

Racial Disparity in Barrett's Esophagus

Odds ratios (ORs) and 95% confidence intervals (CI) will be used to estimate the association between gastroesophageal reflux disease (GERD) and Barrett's esophagus (BE) among Caucasian Americans and African Americans, separately, in relation to patterns of the exposures of interest (tobacco use, alcohol consumption, fruit and vegetable intake and other dietary measures, no NSAID use, and various measures of SES), with adjustments made for the frequency matching factors, age at reference (date of diagnosis for cases and date of identification for controls) and sex.

The promoter regions of Cdxl and Cdx2 genes will be examined for single nucleotide polymorphisms (SNPs). Pyrosequencing will be used to quantitatively determine the methylation status of Cdxl and Cdx2 promoters in esophageal biopsy tissues. For the single functional genotype analyses, conventional unconditional logistic regression will be used and ORs will be estimated for "at-risk" homozygotes and heterozygotes relative to "wild-type" homozygotes by creating indicator variables for each genotype.

Study title	NCT ID	Conditions	Interventions	Eligibility	Organization
Metformin Use to Reduce Disparities in Newly Diagnosed Breast Cancer	NCT04741204	Breast Cancer S... Insulin Resista... Racial Bias	Metformin Exten...	18 Years - 80 Years	Woman's
Metformin Use to Reduce Disparities in Newly Diagnosed Breast Cancer	NCT04741204	Breast Cancer S... Insulin Resista... Racial Bias	Metformin Exten...	18 Years - 80 Years	Woman's
Racial Disparity in Barrett's Esophagus	NCT01374074	Barrett's Esoph... Gastroesophagea... Intestinal Meta...		18 Years - 80 Years	University of North Carolina, Chapel Hill
Metformin Use to Reduce Disparities in Newly Diagnosed Breast Cancer	NCT04741204	Breast Cancer S... Insulin Resista... Racial Bias	Metformin Exten...	18 Years - 80 Years	Woman's
Metformin Use to Reduce Disparities in Newly Diagnosed Breast Cancer	NCT04741204	Breast Cancer S... Insulin Resista... Racial Bias	Metformin Exten...	18 Years - 80 Years	Woman's

Spots Global Cancer Trial Database for racial disparity