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Diabetologia

, Volume 60, Issue 9, pp 1639–1647 | Cite as

Repurposing metformin for the prevention of cancer and cancer recurrence

  • Brandy M. Heckman-Stoddard
  • Andrea DeCensi
  • Vikrant V. Sahasrabuddhe
  • Leslie G. Ford
Review

Abstract

Multiple epidemiological studies have documented an association between metformin, used for treatment of type 2 diabetes, and reduced cancer incidence and mortality. Cell line models may not accurately reflect the effects of metformin in the clinical setting. Moreover, findings from animal model studies have been inconsistent, whilst those from more recent epidemiological studies have tempered the overall effect size. The purpose of this review is to examine metformin’s chemopreventive potential by outlining relevant mechanisms of action, the most recent epidemiologic evidence, and recently completed and ongoing clinical trials. Although repurposing drugs with excellent safety profiles is an appealing strategy for cancer prevention and treatment in the adjuvant setting, there is no substitute for well-executed, large randomised clinical trials to define efficacy and determine the populations that are most likely to benefit from an intervention. Thus, enthusiasm remains for understanding the role of metformin in cancer through ongoing clinical research.

Keywords

Cancer Cancer prevention Cancer recurrence Chemoprevention Metformin Review 

Abbreviations

ACF

Aberrant crypt foci

AMPK

AMP-activated protein kinase

CAV1

Caveolin-1

HNSCC

Head and neck squamous cell carcinoma

MCT4

Monocarboxylate transporter 4

mTOR

Mammalian target of the rapamycin

NSAID

Non-steroidal anti-inflammatory drug

OCT

Organic cation transporter

pS6K

Phospho-serine 6 kinase

SRR

Summary RR

Introduction

Metformin, a biguanide, is the first-line treatment for type 2 diabetes mellitus as an oral glucose-lowering agent. It decreases hepatic gluconeogenesis and improves insulin sensitivity by increasing peripheral glucose uptake and use, lowering both basal and postprandial plasma glucose [1]. It was first approved in the UK in 1958, followed by Canada in 1972, and then the USA in 1994 [2]. The most common side effects that occur in >5% of patients include diarrhoea, nausea/vomiting, flatulence, indigestion, abdominal discomfort, lack of energy and headache [1]. Lactic acidosis is a rare but potentially fatal side effect that can be avoided by checking and monitoring renal function. This tolerable and safe profile, in addition to its low cost as a generic drug, has made metformin an excellent candidate for repurposing. The ease of access to metformin has led to a multitude of preclinical and clinical investigations, as a single agent and in combination with other agents, for both cancer prevention and treatment. According to Web of Science (http://wok.mimas.ac.uk, accessed 15 March 2017), publications on ‘metformin’ AND ‘cancer’ have increased from <40 in 2008 to almost 500 per year in 2015 and 2016, with more than 12,000 citations in 2016. In this review, we provide an update of the recent progress in this field and provide insights into the clinical development of metformin as both a preventive and adjuvant intervention for cancer.

Molecular mechanisms

The potential molecular mechanisms of metformin in cancer prevention and treatment have been extensively reviewed. Metformin is thought to have two potential routes of action that contribute to its anti-neoplastic activity: (1) an indirect route related to its insulin-lowering activity, which may slow tumour proliferation in individuals with hyperinsulinaemia; and (2) direct action in target tissues against respiratory complex I of the electron transport chain in mitochondria of preneoplastic and neoplastic cells, reducing energy consumption in the cell [3]. Both routes of action involve the activation of AMP-activated protein kinase (AMPK) by metformin, which inhibits the mammalian target of the rapamycin (mTOR) pathway, reducing cell proliferation, and inducing apoptosis and cell-cycle arrest [4, 5]. Depending on the target organ, the mechanism of metformin action may be direct, indirect or a combination of the two.

Indirect action of metformin involves the insulin/IGF-1 pathway, which is activated in a setting of nutrient availability [6]. By activating both the phosphatidylinositol-4,5-bisphosphate 3-kinase (PI3K)/Akt/mTOR and the Ras/Raf/mitogen-activated protein kinase (MAPK) pathways, insulin/IGF-1 activity contributes to increased cell growth and proliferation. Metformin decreases hepatic glucose output, increasing muscle uptake of glucose and reducing plasma insulin levels, which in turn may reduce proliferation of both preneoplastic and neoplastic cells. Metformin may also affect cancer cells indirectly through modulation of the immune response [7].

Metformin is hydrophilic (logD [where D is distribution-coefficient] of 26.13 at pH 6.0) and charged at all physiological pH values (pK a [the logarithmic constant of the acid dissociation constant (K a)] is 12.4), requiring transporters to cross the cell membrane for direct action [8]. These include the organic cation transporters (OCT) 1–3, plasma monoamine transporter (PMAT) and the multidrug and toxin extrusion protein (MATE) 1 and 2 [1, 9]; OCT1 is critical for uptake into hepatocytes [10]. The expression of metformin transporters is variable across tumour cell lines and has been shown to be downregulated in breast tumour tissues in comparison with adjacent nonmalignant tissues [11]. In human cancer cell lines, which are known to express OCT1, metformin has been shown to decrease cell proliferation through inhibition of complex I [12]. However, often the transporter expression is not examined in these types of mechanistic, as well as clinical, studies. Furthermore, experiments involving a broad range of cancer cell lines grown in a low-glucose environment suggested that defects in glucose utilisation and mitochondrial function may predict sensitivity to metformin [13]. In women undergoing surgery for ovarian cancer who were taking metformin vs matched women who were not taking metformin, using metabolomics investigators showed metformin to be present in the ovarian tissue along with altered mitochondria metabolism, suggesting a direct effect of metformin on tumours, at clinical doses [14].

In addition to the role of metformin in cellular proliferation and apoptosis, metformin has been shown to inhibit many other cancer pathways. This includes blocking invasion of tumour cells by inhibiting matrix metalloproteinase-9 activation [15], activating growth suppressors through phosphorylation of retinoblastoma protein (pRb) resulting in G0/G1 arrest in prostate cancer cells [16] and inhibiting cancer stem-cell activity [17].

Epidemiological evidence

A substantial body of observational studies, reviewed in numerous systematic reviews, have examined the effect of metformin on overall cancer incidence and mortality, as well as individual cancer sites. Multiple meta-analyses of case–control and cohort studies have now reported a decrease in overall cancer incidence of approximately 10 to 40% with metformin use, along with a decrease in mortality by a similar range [18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28] (Table 1, modified from [29]). In contrast, meta-analyses of RCTs have shown a non-significant change in cancer incidence [22, 23, 24, 28]; however, the randomised trials included were conducted to treat diabetes or reduce cardiovascular events and had baseline median ages ranging from 47 to 60 and short follow-up time, making them underpowered to detect an effect on cancer incidence. We also performed a meta-analysis, paying particular attention to biases and confounders following a review by Suissa and Azoulay underscoring the prevalence of time-related biases in observational studies and their potential to inflate estimates of the protective effect of metformin [30]. Similar to prior studies, we found the overall reduction of cancer incidence with metformin use was 30 to 40%; however, excluding time-biased studies, the reduction in overall cancer incidence was only 10%, albeit still statistically significant [24].
Table 1

Meta-analyses examining the effect of metformin use on cancer incidence and mortality

Study authors (date)

Association of metformin use with overall cancer incidence, SRR (95% CI)

Association of metformin use with overall cancer mortality, SRR (95% CI)

DeCensi et al (2010) [18]

0.68 (0.52, 0.88)

0.70 (0.51, 0.96)

Noto et al (2012) [20]

0.67 (0.53, 0.85)

0.66 (0.49, 0.88)

Soranna et al (2012) [21]

0.61 (0.54, 0.70)

ND

Stevens et al (2012) [28]

1.02 (0.82, 1.26)a

ND

Thakkar et al (2013) [22]

1.01 (0.81, 1.26)a

0.70 (0.67, 0.73)b

0.90 (0.84, 0.98)c

ND

Franciosi et al (2013) [19]

0.98 (0.81, 1.19)a

0.73 (0.61, 0.88)

0.65 (0.53, 0.80)

Zhang et al (2013) [25]

0.73 (0.64, 0.83)

0.82 (0.76, 0.89)

Lega et al (2014) [26]

ND

0.74 (0.62, 0.88)

Zhang and Li (2014) [27]

ND

0.70 (0.55, 0.88)

Gandini et al (2014) [24]

0.69 (0.52, 0.90)

0.95 (0.69, 1.30)a

0.90 (0.89, 0.91)d

0.66 (0.54, 0.81)

Wu et al (2015) [23]

0.86 (0.83, 0.90)

1.05 (0.94, 1.18)a

0.88 (0.83, 0.92)b

0.71 (0.63, 0.80)c

0.70 (0.53, 0.94)

0.91 (0.37, 2.23)a

0.66 (0.49, 0.89)b

Table modified from [26]

aRCT

bCohort study

cCase–control study

dAdjusted for time bias

ND, no data

Metformin has been associated with a decreased risk of breast, colon, liver, pancreas, prostate, endometrium and lung cancer across meta-analyses. Besides time bias, individual organ-specific confounders are also important. For lung cancer, overall and time-unbiased analyses point to a protective effect of metformin with a summary RR (SRR) of 0.82 (95% CI 0.67, 0.99), whereas adjustment for smoking, the leading cause of lung cancer, resulted in loss of significance with an SRR of 0.95 (95% CI 0.82, 1.11). A recent meta-analysis that focused on the role of metformin and colorectal adenoma, a precursor to colorectal cancer, showed a pooled OR of 0.76 (95% CI 0.63, 0.92). However, they also noted publication bias against negative studies [31]. Metformin use has previously been shown to be associated with a reduced risk of colorectal cancer [32, 33, 34].

Compared with cancer incidence, the effect of metformin on cancer mortality is informed by fewer studies and, thus, site-specific analyses of the effects of metformin on overall mortality have not been performed in older meta-analyses [24]. However, more recent meta-analyses have focused on the impact of metformin on site-specific cancer mortality and overall survival, as reviewed in Table 2 [26, 27, 35, 36, 37, 38, 39, 40, 41, 42, 43]. These analyses have shown marked reductions in cancer-specific mortality for colon, lung and early-stage prostate cancer, and improvements in overall survival for breast, colon, gynaecological (endometrial and ovarian), liver, lung, prostate and pancreatic cancer.
Table 2

Meta-analyses examining the effect of metformin use on cancer site-specific mortality

Cancer Site

Study authors (date)

Association of metformin use with cancer site-specific mortality, HR (95% CI)

Association of metformin use with overall mortality, HR (95% CI)

Breast

Yang et al (2015) [35]

ND

0.70 (0.51, 0.96)

Colon

Lega et al (2014) [26]

Zhang and Li (2014) [27]

Coyle et al (2016) [39]

0.65 (0.56, 0.76)

ND

0.58 (0.39, 0.86)

ND

0.70 (0.59, 0.84)

0.69 (0.58, 0.83)

Endometrial

Perez-Lopez et al (2017) [36]

ND

0.64 (0.45, 0.89)

Liver

Ma et al (2016) [37]

ND

0.59 (0.42, 0.83)

Lung

Wan et al (2016) [38]

Tian et al (2016) [42]

0.65 (0.52, 0.83)

ND

0.78 (0.64, 0.93)

0.90 (0.84, 0.96)

Ovarian

Zhang and Li (2014) [27]

ND

0.44 (0.30, 0.64)

Prostate

Raval et al (2015) [43]

Coyle et al (2016)a [39]

Stopsack et al (2016) [40]

0.76 (0.43, 1.33)

0.58 (0.37, 0.93)

0.76 (0.44, 1.31)

0.86 (0.67, 1.10)

0.82 (0.73, 0.93)

0.88 (0.86, 0.90)

Pancreas

Zhou et al (2017) [41]

ND

0.84 (0.73, 0.96)

aStudy focused on localised, early-stage disease

ND, no data

Taken together, these results point out the inconsistent evidence from epidemiological studies that often do not completely capture or misclassify important information prior to analysis, such as the dose and duration of metformin therapy, diabetes history (duration and progression diabetes), changes in glucose-lowering medications, and the potential that participants may be taking multiple combined glucose-lowering medications [44]. Therefore, while most studies, including our meta-analysis, suggest that metformin use is associated with a reduced risk of cancer and death from cancer, the effect size may be smaller than previously believed.

Reported clinical trials

To date, there are 17 clinical trials that have examined the effect of metformin on cancer related biomarkers and reported results (Table 3; adapted from [29]). The studies were conducted in various disease settings, spanning at-risk participants, individuals with preneoplastic lesions, individuals who were awaiting surgical excision, and those receiving metformin in an adjuvant setting.
Table 3

Completed clinical trials examining the effect of metformin on cancer biomarkers

Organ site; Trial phase; Trial registration numbera

Study design

Study population

Planned accrual (n); evaluable (n)

Primary outcomed

Barrett’s oesophagus; Phase II; NCT01447927 [45]

500–2000 mg/day (dose-escalated); for 12 weeks; metformin vs placebo

Barrett’s oesophagus ≥2 cm in length; daily PPI for ≥4 weeks; without high-grade dysplasia

74; 74

No significant change in pS6K levels; metformin vs placebo

Breast; Phase II [46]b

500 mg three times per day for 6 months

Women with IBC who completed therapy with fasting insulin ≥45 pmol/l and glucose <7.0 mmol/l

40; 22

22.4% decrease in insulin levels (p = 0.024)

Breast; Phase II; 2006–006236-22 [48]

1000 v. 1500 mg/day for 3 months

Postmenopausal women with a history of IBC; 6 months post-surgery; on tamoxifen for at least 6 months, planning to continue use; or at least 6 months post chemotherapy

125; 96

1500 mg/day decreased testosterone levels by 23% (p < 0.01) vs 1000 mg/day

Breast; Phase IV; 2007–000306-70 [49]

500 mg/day for 1 week followed by 1000 mg/day for 1 week; metformin vs placebo

IBC Stage 1–2; >1 cm; without history of diabetes

47; 39

3.4% decrease in Ki-67 (p = 0.027); metformin vs placebo

Breast; Phase II; 2008–004912-10 [50]

850 mg/day for 3 days followed by 850 mg twice daily (day 4–28) for 4 weeks prior to surgery; metformin vs placebo

Women; presurgical; without IBC Stage I–III (not suitable for neoadjuvant therapy)

200; 196

No overall change in Ki-67; 10.5% decrease in Ki-67 if HOMA-IR >2.8 (p for interaction = 0.045); metformin vs placebo

Breast; NCT00897884c [51]

500 mg twice daily for 2–3 weeks

Women; aged <70; presurgical; IBC Stage I–IV

48; 39

3% decrease in Ki-67 (p = 0.016)

Breast; Phase II (pilot study); NCT00930579 [52]

500 mg in morning and 1000 mg in the evening for 2 weeks

Women; presurgical; DCIS or operable IBC; BMI >25 kg/m2

40; 32

No change in Ki-67

Colon; Phase III [53]

UMIN000001241

250 mg/day for 4 weeks; metformin vs control (untreated)

Presence of ACFs; without concurrent use of NSAIDs

26; 23

Mean (± SD) number of ACFs decreased from 8.78 (± 6.45) to 5.11 (± 4.99) in metformin arm (p = 0.007) vs control

Colon; Phase III [54]

UMIN000006254

250 mg/day for 1 year; metformin vs placebo

Prior single or multiple colorectal adenomas resected by endoscopy

151; 143

Polyps RR 0.67 (95% CI 0.47, 0.97); Adenomas RR 0.60 (95% CI 0.39, 0.92); metformin vs placebo

Colon; Phase II; NCT01312467

500 mg/day on days 1–7, followed by 1000 mg/day on days 8–14, 1500 mg/day on days 15–21 and 2000 mg/day from day 22 to end of study endoscopy

Age 35–80; history of adenoma in previous 3 years; BMI ≥30 kg/m2

45; 32

Non-significant change in pS6K Ser235

Endometrial; early Phase I; NCT01911247 [55]

850 mg/day for 1–4 weeks prior to surgery

BMI ≥30 kg/m2; confirmed type 1 endometrial cancer

28; 20

11.75% reduction in Ki-67 (p = 0.008)

Endometrial; UMIN000004852c [56]

750 mg/day, increasing to 2250 mg/day if no side effects occurred prior to surgery

Women aged 20–70; histologically confirmed endometrial adenocarcinoma Grade 1–2, without myometrium invasion

40; 31

44.2% decrease in Ki-67 (p < 0.001)

Endometrial; Phase II; 2011–001382-40 [57]

850 mg twice daily for 1–4 weeks prior to surgery; metformin vs control (untreated)

Biopsy-proven endometrial adenocarcinoma or hyperplasia; scheduled for hysterectomy

30; 28 (metformin)/

12 (control)

17.2% decrease in Ki-67 (p = 0.002; adjusted mean difference); metformin vs control

Endometrial; Phase II (pilot); UMIN000002210 [58]

400 mg/day MPA and 100 mg/day aspirin for 24 weeks followed by 1 mg norethisterone and 0.035 mg ethinylestradiol per day for six menstrual cycles, with 750 mg/day metformin (increased to 1500 mg/day if no side effects) taken continuously for 4 years

Histologically well-differentiated endometrial adenocarcinoma at presumed Stage IA, and atypical endometrial hyperplasia

38; 36

Two patients had progression to advanced cancer at 12 weeks; at 36 weeks, 29 patients had complete response (regression of disease) and five had partial response (down-staging of disease)

Head and neck; early Phase I; NCT02083692 [59]

500 mg/day on days 1–3, followed by 500 mg twice daily on days 4–6 and 1000 mg twice daily starting on day 7 for 9–28 days

Biopsy-proven head and neck cancer with planned definitive resection

40; 33

Significant increase in stromal CAV1 (p < 0.001); no significant change in stromal MCT4 expression

Prostate; Phase II; NCT00881725 [60]

500 mg three times daily for 4–12 weeks prior to surgery

Confirmed prostate cancer; scheduled for prostatectomy

40; 22

29.5% decrease in Ki-67 (p = 0.006)

Prostate; Phase II; NCT01433913

500 mg/day on days 1–7, followed by 1000 mg/day on days 8–14 and 1500 mg/day on day 22 to surgery; total study length: 4–12 weeks; metformin vs placebo

Men scheduled for prostatectomy

20; 19

Mean Ki-67% (± SD): 6.38 (± 3.41) (metformin); 5.19 (± 4.95) (placebo)

Table adapted from [26]

aTrial registered on ClinicalTrials.gov, EU Clinical Trials Register or University Hospital Medical Information Network Clinical Trials Registry (UMIN-CTR). Phase classification is given as registered on the site or as detailed in the reference

bCompleted prior to ClinicalTrials.gov registration requirement, therefore, clinical trial number is not available

cDetails of phase classification not given

dOutcomes are vs baseline unless otherwise stated

DCIS, ductal carcinoma in situ; IBC, invasive breast cancer; MPA, medroxyprogesterone acetate; PPI, proton pump inhibitor;

A multicentre randomised trial of metformin in individuals with Barrett’s oesophagus who were taking a proton pump inhibitor showed no significant change in phospho-serine 6 kinase (pS6K), a biomarker of insulin pathway activation, comparing baseline endoscopy biopsies with end of study biopsies [45]. Non-steroidal anti-inflammatory drug (NSAID) use was allowed in the study to aid patient accrual. Since NSAIDs are associated with decreased cancer risk, this may have affected the study’s ability to observe an effect.

Two studies examined various doses of metformin given for 3 to 6 months to women after completion of chemotherapy and radiation for breast cancer [41, 42]. The first study examined specifically selected women whose plasma levels of insulin were at least 45 pmol/l [46]. This group was selected based on a prior cohort study that showed women with these characteristics were at an increased risk of breast cancer [47]. In this study, metformin decreased circulating insulin levels by 22.4% (p = 0.024) [46]. The second study enrolled women with elevated testosterone levels and compared two doses of metformin (1000 mg/day vs 1500 mg/day); the higher dose significantly reduced serum testosterone levels and free androgen index compared with the lower dose [48]. These findings demonstrate that metformin could reduce serum markers associated with breast cancer risk.

Four trials have examined the short-term effects (1–4 weeks) of various doses of metformin on cell proliferation (as assessed by the expression of Ki-67) in tissues from women awaiting surgery for breast cancer (presurgical trials) [44, 45, 46, 47]. One of these trials found a 3.4% reduction in Ki-67 (p = 0.027) in the metformin arm, comparing biopsies at diagnosis with biopsies at the time of surgery [49]. However, in the largest randomised, double-blind, placebo-controlled study of the effect of metformin on Ki-67 expression in breast cancer, the change in Ki-67 between diagnostic biopsy and surgical specimen was not significant relative to placebo [50]. Although, women with higher insulin resistance (HOMA-IR >2.8) had a non-significant decrease in Ki-67 expression of 10.5%, while women with no/lower insulin resistance (HOMA-IR <2.8) had a non-significant increase in expression (11.1%). The interaction between insulin resistance (as measured by the HOMA-IR) and metformin with regard to Ki-67 expression was statistically significant (p = 0.045) [50]. A third, single-arm trial reported a decrease in Ki-67 levels, from 36.5% to 33.5% (p = 0.016), after a median of 18 days of metformin treatment (diagnostic biopsy vs surgical specimen) [51], while a recently completed study in a majority Hispanic population with a historical control group matched for age, BMI and stage, showed no reduction in Ki-67 in the metformin arm or in the untreated control group, when baseline biopsies were compared with surgical excisional specimens [52].

Multiple studies have examined the effect of metformin on colon cancer prevention. The number of aberrant crypt foci (ACF; a putative precursor of colon cancer) was examined in individuals with pre-existing ACF, randomising participants to very low dose metformin (250 mg/day) or no treatment for 1 month [53]. A significant decrease in ACF (mean ± SD), from 8.78 ± 6.45 to 5.11 ± 4.99 (p = 0.007), was observed in the metformin arm but not in the control group. A follow-up Phase III, multicentre, double-blind, placebo-controlled trial performed by the same group randomised participants with a history of colorectal adenoma to either metformin at 250 mg/day (n = 151) or placebo (n = 143) for 1 year. Seventy-one participants in the metformin arm and 62 in the placebo group had an end-of-study colonoscopy and the RR of adenomas was 0.60 (95% CI 0.39, 0.92) [54]. A multicentre single-arm study also examined a similar population with a history of adenoma in the previous 3 years, with BMI ≥30 kg/m2. Participants were given metformin at an escalating dose, from 500 to 2000 mg/day for 12 weeks. No significant changes in the primary endpoint, pS6K levels, were observed (ClincalTrials.gov registration no. NCT01312467).

The role of metformin in endometrial cancer prevention is of particular interest because of the strong association between endometrial cancer and obesity, and the use of metformin for the treatment of polycystic ovary syndrome, a common condition that is associated with increased risk of endometrial cancer. Four studies have been reported in women with early-stage endometrial cancer and/or endometrial hyperplasia who were treated with metformin prior to hysterectomy [51, 52, 53, 54, 55]. Among women with Stage 1–2 endometrioid endometrial cancer and a BMI ≥30 kg/m2, treatment with 850 mg/day metformin resulted in an 11.75% reduction in Ki-67 (p = 0.008) [55]. In addition, using serum metabolomics, this study showed a greater modulation in lipid metabolism among metformin responders vs non-responders, which the authors suggest support an indirect mechanism of metformin action on cell proliferation [55]. Another study in individuals with endometrioid endometrial cancer with dosage escalation of metformin from 750 mg/day to 1500 mg/day or 2250 mg/day (based on the individual’s tolerance of metformin), for 4 weeks prior to surgery showed a 44.2% decrease in Ki-67 with metformin use (p < 0.001), with no significant change in the untreated historical control group [56]. This study also examined the concentration of metformin in endometrial tissue, which was found to be 1.2–5.1 μmol/kg wet weight (approximately 20% of that in plasma), demonstrating that metformin was present in the endometrium [56]. In a non-randomised study of women with biopsy-proven endometrial hyperplasia or endometrioid endometrial cancer, 28 women were treated with 850 mg of metformin twice daily, while 12 women received no drug. A significant adjusted mean difference in Ki-67 of −17.2% (p = 0.002) was observed in the metformin group vs control group [57]. Another study examined fertility preservation in women with endometrial hyperplasia or Grade 1 endometrial cancer using dose-escalated metformin therapy, from 750 mg/day to 1500 mg/day, in combination with 400 mg/day medroxyprogesterone acetate and 100 mg/day aspirin for 24 weeks, followed by a low-dose monophasic agent (1 mg norethisterone and 0.035 mg ethinylestradiol per day) for six menstrual cycles [58]. Two participants showed progression to advanced cancer at 12 weeks, while 29 achieved a complete response (regression of disease) and five had a partial response (down-staging of disease) at 36 weeks, with 16 of these individuals going on to conceive [58].

A single study has examined the role of metformin in head and neck squamous cell carcinoma (HNSCC) prior to surgery, with change in stromal caveolin-1 (CAV1) and monocarboxylate transporter 4 (MCT4) as the primary endpoint, with the rationale that metformin targets cells with altered glycolysis, which has been shown in cancer-associated fibroblasts particularly in HNSCC [59]. Low CAV1 and increased MCT4 levels are associated with aggressive disease in HNSCC. The study showed a significant increase in CAV1 but no change in MCT4 in 33 evaluable participants between baseline biopsy and surgical specimen [59].

Finally, two studies have evaluated metformin in men with prostate cancer treated with metformin (500 mg three times daily) for 4–12 weeks prior to surgery [56, 57]; a single-arm study examined change in Ki-67, comparing diagnostic biopsy with tissue from prostatectomy, showing an absolute decrease in the Ki67 proliferation index (percentage of nuclei showing nuclear immunoreactivity of any intensity) of 1.44%, which amounted to a statistically significant relative decrease from baseline of 29.5% (p = 0.006) [60]. The second randomised study demonstrated no difference in cell proliferation in prostatectomy samples between eight individuals in the metformin group (mean Ki-67, 6.38%) at surgery compared with nine individuals in the placebo group at surgery (mean Ki-67, 5.19%) (ClinicalTrials.gov registration no. NCT01433913). Baseline Ki-67 was not evaluated in this study. This study also evaluated metformin concentration in the prostate tissue, but the data are not yet published.

Ongoing clinical trials

An analysis of clinical trials registered on ClinicalTrials.gov (https://clinicaltrials.gov/, accessed 15 March 2017) revealed an additional 23 trials examining the effect of metformin in participants at risk of cancer, 30 presurgical studies and 30 studies in the adjuvant setting. This is a significant increase from a similar analysis of ongoing studies conducted in 2011, in which there were three studies examining the effect of metformin in participants at risk for cancer, nine presurgical studies and seven studies in the adjuvant setting. The ongoing studies examine similar endpoints, including pharmacodynamic markers, such as tumour/tissue levels of pS6K, or other measures of AMPK signalling. Many of the studies examine surrogate endpoints for cancer, such as atypia or breast density for breast cancer, or change in prostate specific antigen (PSA) for prostate cancer. As has been reported in many studies, accrual to clinical trials is challenging with many pilot studies closing because of poor accrual.

Building on results from early phase studies (described above) and other preclinical and observational epidemiological data, several Phase III studies are currently (2017) ongoing. For example, a Phase III randomized, placebo-controlled study in men with biopsy-proven, low-risk localised prostate cancer, undergoing active surveillance, is examining time to progression of prostate cancer with metformin (ClinicalTrial.gov registration no. NCT01864096). Further, the National Cancer Institute of Canada (NCIC) MA.32 trial, a Phase III adjuvant breast cancer trial, has randomised 3649 women within 12 months of diagnosis who have completed chemotherapy and radiation to metformin 850 mg twice a day (850 mg/day during weeks 1–4) vs placebo for 5 years (ClinicalTrial.gov registration no. NCT01101438). The primary endpoint is invasive disease-free survival. This study is fully accrued with an estimated completion date of July 2020. There was also a Phase III study planned in 408 individuals with hepatitis C liver cirrhosis, examining treatment with 1000 mg twice daily metformin vs placebo for 36 months, with the primary endpoint of rate of hepatocellular carcinoma occurrence and liver-related death or transplantation. This study was started in June 2015 but was terminated at the decision of the investigator in April 2016 after 11 participants were accrued (ClinicalTrial.gov registration no. NCT02319200). The Diabetes Prevention Program was a Phase III study that started in 1996 to examine the influence of metformin and intensive lifestyle intervention compared with placebo on progression from impaired glucose tolerance to diabetes. The follow-up to this study (the Diabetes Prevention Program Outcomes Study [ClinicalTrial.gov registration no. NCT00038727]) has continued to actively follow this cohort, with open-label use of metformin in the original metformin arm, to examine progression to diabetes as well as the development of long-term diabetes complications. The study group has also retrospectively collected medical records for cancer that have been reported over the course of the study and will continue to collect data on cancer outcomes as part of an extension to the original clinical trial [61]. This study is unique because of the extensive length of longitudinal follow-up, the use of glucose tolerance tests to robustly identify disease (diabetes) onset, and availability of excellent data on dosing, exposure and compliance to metformin.

Conclusions

There is a long history and much clinical experience with metformin that makes it a very attractive candidate for drug repurposing for cancer prevention. Data on the potential mechanisms of metformin action for cancer prevention and treatment, as well as additional longitudinal epidemiological data from new and previously examined cohorts, continues to accumulate. There is biological plausibility for a cancer preventive effect of metformin, given multiple ways that it can interfere with cancer promoting signalling pathways. However, both animal and epidemiological studies have shown somewhat mixed effects. The epidemiological literature has largely evaluated individuals with diabetes, and the cancer-preventive effect is of lesser magnitude than previously reported once appropriate adjustments have been made to account for various biases and confounders. It remains to be determined whether a similar protective effect can be demonstrated in individuals without diabetes or in individuals with impaired fasting glucose. Multiple clinical trials have reported promising results, but Phase III studies are ongoing and these will provide the best evidence. Cancer is not one disease and each cancer subtype may respond to metformin in a unique way. Additional studies may be needed as data becomes available to elucidate those that are most likely to benefit from metformin treatment for the prevention of cancer and its recurrence.

Notes

Acknowledgements

This material should not be interpreted as representing the viewpoint of the US Department of Health and Human Services, the National Institutes of Health, or the National Cancer Institute.

Funding

Work in AD’s laboratory is supported by grants from the Italian Association for Cancer Research (AIRC) and from TRANSCAN-ERANET (JTC 2013-056).

Duality of interest

The authors declare that there is no duality of interest associated with this manuscript.

Contribution statement

All authors participated in drafting the article and revising it critically for important intellectual content. All authors approved the version to be published.

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Copyright information

© US Government (outside the USA) 2017

Authors and Affiliations

  • Brandy M. Heckman-Stoddard
    • 1
  • Andrea DeCensi
    • 2
    • 3
  • Vikrant V. Sahasrabuddhe
    • 1
  • Leslie G. Ford
    • 1
  1. 1.Division of Cancer PreventionNational Cancer InstituteBethesdaUSA
  2. 2.Division of Medical OncologyEnte Ospedaliero Ospedali GallieraGenoaItaly
  3. 3.Wolfson Institute of Preventive MedicineQueen Mary University of LondonLondonUK

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