Metformin in early breast cancer: a prospective window of opportunity neoadjuvant study

被引:222
作者
Niraula, Saroj [1 ,2 ]
Dowling, Ryan J. O. [3 ]
Ennis, Marguerite
Chang, Martin C. [4 ,5 ]
Done, Susan J. [5 ,6 ,7 ]
Hood, Nicky [8 ]
Escallon, Jaime [9 ,10 ]
Leong, Wey Liang [10 ,11 ]
McCready, David R. [9 ,10 ]
Reedijk, Michael [10 ,11 ]
Stambolic, Vuk [3 ]
Goodwin, Pamela J. [1 ,2 ,8 ]
机构
[1] Mt Sinai Hosp, Dept Med, Div Med Oncol & Hematol, Toronto, ON M5G 1X5, Canada
[2] Univ Toronto, Princess Margaret Hosp, Toronto, ON M5G 1X5, Canada
[3] Univ Hlth Network, Ontario Canc Inst, Toronto, ON, Canada
[4] Mt Sinai Hosp, Dept Pathol & Lab Med, Toronto, ON M5G 1X5, Canada
[5] Univ Toronto, Dept Lab Med & Pathobiol, Toronto, ON M5G 1X5, Canada
[6] Univ Hlth Network, Campbell Family Inst Breast Canc Res, Toronto, ON, Canada
[7] Univ Hlth Network, Lab Med Program, Toronto, ON, Canada
[8] Mt Sinai Hosp, Div Clin Epidemiol, Samuel Lunenfeld Res Inst, Toronto, ON M5G 1X5, Canada
[9] Univ Toronto, Dept Surg, Mt Sinai Hosp, Toronto, ON M5G 1X5, Canada
[10] Univ Toronto, Univ Hlth Network, Dept Surg Oncol, Toronto, ON M5G 1X5, Canada
[11] Princess Margaret Hosp, Campbell Family Inst Breast Canc Res, Toronto, ON M4X 1K9, Canada
基金
加拿大健康研究院;
关键词
Breast cancer; Metformin; Neoadjuvant; Ki67; TUNEL; Insulin; DIABETIC-PATIENTS; INSULIN-RECEPTOR; APOPTOSIS; PROLIFERATION; RECOMMENDATIONS; CHEMOTHERAPY; RESPONSES; MODEL; RISK; KI67;
D O I
10.1007/s10549-012-2223-1
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Metformin may exert anti-cancer effects through indirect (insulin-mediated) or direct (insulin-independent) mechanisms. We report results of a neoadjuvant "window of opportunity" study of metformin in women with operable breast cancer. Newly diagnosed, untreated, non-diabetic breast cancer patients received metformin 500 mg tid after diagnostic core biopsy until definitive surgery. Clinical (weight, symptoms, and quality of life) and blood [fasting serum insulin, glucose, homeostasis model assessment (HOMA), C-reactive protein (CRP), and leptin] attributes were compared pre- and post-metformin as were terminal deoxynucleotidyl transferase-mediated dUTP nick end labeling (TUNEL) and Ki67 scores (our primary endpoint) in tumor tissue. Thirty-nine patients completed the study. Mean age was 51 years, and metformin was administered for a median of 18 days (range 13-40) up to the evening prior to surgery. 51 % had T1 cancers, 38 % had positive nodes, 85 % had ER and/or PgR positive tumors, and 13 % had HER2 overexpressing or amplified tumors. Mild, self-limiting nausea, diarrhea, anorexia, and abdominal bloating were present in 50, 50, 41, and 32 % of patients, respectively, but no significant decreases were seen on the EORTC30-QLQ function scales. Body mass index (BMI) (-0.5 kg/m(2), p < 0.0001), weight (-1.2 kg, p < 0.0001), and HOMA (-0.21, p = 0.047) decreased significantly while non-significant decreases were seen in insulin (-4.7 pmol/L, p = 0.07), leptin (-1.3 ng/mL, p = 0.15) and CRP (-0.2 mg/L, p = 0.35). Ki67 staining in invasive tumor tissue decreased (from 36.5 to 33.5 %, p = 0.016) and TUNEL staining increased (from 0.56 to 1.05, p = 0.004). Short-term preoperative metformin was well tolerated and resulted in clinical and cellular changes consistent with beneficial anti-cancer effects; evaluation of the clinical relevance of these findings in adequately powered clinical trials using clinical endpoints such as survival is needed.
引用
收藏
页码:821 / 830
页数:10
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