Metformin use and its effect on survival in diabetic patients with advanced non-small cell lung cancer

In Mexico, more than 95 % of all patients with non-small cell lung cancer (NSCLC) present with advanced-stage disease at the time of diagnosis [1]. Because the prevalence of type 2 diabetes is high both worldwide and in Mexico, it is very important to understand the effects of preexisting diabetes on the survival of patients with advanced NSCLC. The physiopathology of diabetes, the effects of its treatment and the changes in different organ systems observed in diabetic patients might be associated with clinical outcomes. Existing data regarding the effects of diabetes on NSCLC outcomes are conflicting. Although some early studies found longer survival rates in diabetic patients with NSCLC [2], this result was not confirmed in other larger series [3, 4]. Indeed, an elevated fasting glucose level was found to be independently associated with a significantly higher risk of mortality in patients with NSCLC [3].

Among the major hypoglycemic agents that are used for the treatment of diabetes, metformin has received the most attention regarding its potential antineoplastic uses. At the cellular level, metformin has profound effects on the mitochondrial respiration rate and the production of ATP [5]. Metformin affects multiple cellular pathways via the activation of AMP-activated protein kinase (AMPK) by liver kinase 1 (LKB1), which leads to decreases in growth factor signaling and proliferation via the inhibition of mTOR [6].

There is a general lack of information regarding the outcomes of diabetic patients with NSCLC who are treated with different antidiabetic agents, including metformin, and the published data come from large epidemiological databases that are prone to bias [7]. In this study, our objective was to analyze the effects of diabetes and its treatment in terms of the survival of patients with NSCLC.

We conducted a retrospective cohort observational study. Consecutive patients diagnosed with NSCLC at the Instituto Nacional de Cancerología (INCan) between January 2008 and December 2014 were retrieved from our electronic medical records. The study was approved by INCan’s research committee (REV/05/16). Because the study was deemed as without risk, patient consent was not required. The patient and tumor characteristics, including age, comorbidities, body mass index, stage at diagnosis, tobacco use, wood smoke exposure and mutational analysis results, were obtained. All patients were staged using thoracic and abdominal CT scans, PET scans and MRI imaging of the central nervous system. Previous diagnoses of diabetes, current antidiabetic treatments and glucose measurements for each individual patient were also recorded at the time of the lung cancer diagnosis. The patients were considered to have a diagnosis of diabetes if they either fulfilled the American Diabetes Association (ADA) criteria for diabetes or were being treated with antidiabetic medications prior to diagnosis with NSCLC. The patients were treated according to published guidelines for the treatment of lung cancer [8]. Patients with missing data were excluded from the analysis.

Proper glycemic control was defined by a pre-prandial (fasting) glucose level of 70–130 mg/dL at the time of the lung cancer diagnosis, in accordance with the current guidelines of the ADA [9]. Because most patients lacked a measurement of glycated hemoglobin (HbA1C), we calculated the mean plasma glucose by averaging the patient’s pre-prandial glucose measurements (at least 3). We considered patients with mean plasma glucose levels under 130 mg/dL to be within the proper glycemic control goals and those with a mean plasma glucose level over 130 mg/dL to have improperly controlled diabetes. The overall survival (OS) was calculated from the date of cancer diagnosis to the date of the last visit or death.

The de-identified patient dataset supporting the conclusions of this article is included within the article and its additional supporting file (Additional file 1).

Our results revealed that both the use of metformin and the maintenance of proper glycemic control are related to improved survival in the diabetic patients with advanced NSCLC. In our population, the use of metformin and the maintenance of proper glycemic control affected survival, independent of stage, histology and other antidiabetic treatments. Our results suggest that treatment with metformin, but not other hypoglycemic agents, is associated with a significant improvement in survival in patients with NSCLC and diabetes.

Evidence from epidemiological studies and meta-analyses has demonstrated associations of diabetes with several malignancies, including pancreatic [10], breast [11], prostate [12], colonic [13] and hepatocellular carcinomas [14]. In contrast, the relationship between diabetes and NSCLC is not well established, and epidemiological data have yielded conflicting results. Although some studies have reported an association between diabetes and NSCLC [15, 16], the majority has reported null or inverse relationships [17‐19]. This potentially negative relationship is further illustrated by the fact that NSCLC has not been found to be associated with obesity, which is strongly related to the presence of diabetes [20]. Indeed, a high body mass index has been found to be a protective factor against NSCLC in some studies [21]. Further, a recently published meta-analysis by Zhang et al. concluded that metformin use in patients with diabetes appears to be associated with a reduced risk of lung cancer. This area requires further study and should be considered in the treatment of patients with diabetes and NSCLC [22].

The association between diabetes mellitus and survival in lung cancer patients is controversial [23] Whereas some studies suggest that patients with diabetes mellitus have worse prognoses due to comorbidities and disease complications that can be related to a reduced tolerance of treatment [24, 25], other studies have demonstrated that diabetic patients exhibited increased survival compared with non-diabetics [7, 26, 27]. The contradictory results between different studies might be the consequence of the analyses of heterogeneous populations. In the present study, we found that diabetes mellitus was not associated with an improved OS in all patients; however, our findings demonstrated that the diabetic patients with proper glycemic control exhibited a better OS than did the other diabetic patients and even the non-diabetics, which is consistent with previously published data [26].

Metformin has been explored as a pharmacological agent that may improve the survival of patients with several types of cancer. A recent meta-analysis reported associations between metformin and prolonged survival in patients with breast, colorectal, ovarian and endometrial cancers [28]. In NSCLC patients, the benefit of metformin on the prognosis has been demonstrated in large epidemiological studies [11] and in a meta-analysis [29]. Unfortunately, the main limitation of these studies is that they included heterogeneous patients and treatments and were thus prone to bias. In contrast, our report included a large set of NSCLC patients who were treated at a single reference institution where the prevalence of diabetes is high.

One potential explanation for the beneficial effects of metformin and proper glycemic control is that both are related to a reduction in circulating insulin levels. Insulin can stimulate both the insulin receptor (IR) and the insulin-like growth factor-1 receptor (IGF-1R), and both of these receptors are overexpressed in NSCLC patients and correlated with worse prognoses [30] and poor responses to targeted treatments [31]. Metformin has been demonstrated to interact with IGF signaling to reduce both the proliferation and migration of cancer cells [29]. There is a growing body of evidence regarding the effects of metformin on the multiple pathways that regulate carcinogenesis. Metformin inhibits mTOR translation initiation, the epithelial-mesenchymal transition (EMT), IL-6 secretion and STAT3 activity [32]. Thus, several preclinical experiments have tested combinations of metformin with radiotherapy [33], chemotherapy [34] and targeted therapies in lung cancer patients to overcome the mechanisms of resistance and to achieve synergy [35]. Metformin has been demonstrated to sensitize EGFR tyrosine kinase inhibitor (TKI)-resistant lung cancer cells by reversing the EMT and decreasing IL-6 signaling activation [32]. The combination of gefitinib (a reversible EGFR-TKI) and metformin induces a strong antiproliferative effect in NSCLC cell lines that harbor the wild-type LKB-1 gene [36]. Antiproliferative synergism between metformin and the multikinase inhibitor sorafenib via AMPK activation has also been demonstrated in NSCLC cells that harbor KRAS mutations [37]. Taken together, these data have led to the design of clinical trials utilizing combinations of metformin and targeted therapies for NSCLC patients who harbor specific mutations [38]. The ALMERA trial is an ongoing phase II trial conducted by the Ontario Clinical Oncology Group that will provide prospective evidence regarding the potential of metformin to improve the outcomes of standard cytotoxic therapy in locally advanced NSCLC patients [39].

Due to its retrospective nature, our study has some inherent limitations. HbA1c measurements were not available for the majority of the patients; therefore, we were unable to clearly identify patients with proper glycemic control. To resolve this issue, we calculated the mean plasma glucose levels using the fasting measurements from each patient. Although it was not ideal, this approach yielded the expected results in terms of the comparisons of the patient groups. Additionally, due to the retrospective nature of the data, we were unable to assess whether the patients who were not taking metformin had specific contraindications for its use or whether the patients with metformin prescriptions properly adhered to their treatment regimen. Furthermore, we had no data regarding whether patients who failed to achieve proper glycemic control were undergoing different types of treatment (e.g., chemotherapy rather than targeted therapy) that might have included high-dose steroids or had negative effects on proper adherence.

It is important to mention that our patients exhibited particularly prolonged average OS despite having advanced stage NSCLC. This finding may have resulted from the large incidence of EGFR-mutated tumors in our population [40, 41] and the broad access to clinical trials available at our institution. Some retrospective studies have associated the use of metformin with a lower risk of lung cancer, but the designs of these studies have been questioned due to time-related bias [42, 43]. To reduce the risk of this bias, both metformin use and proper glycemic control were assessed at the time of the lung cancer diagnoses.

It is possible that patients undergoing cytotoxic chemotherapy rather than targeted therapy would be more likely to stop taking metformin or that the drug could have different effects depending on the mutational statuses of the patients. However, the small number of EGFR and KRAS patients taking metformin made it difficult to draw any conclusions regarding these particularly interesting populations.

Finally, we were unable to gather data about the related metabolic comorbidities, such as waist circumference and lipid levels. However, given that mortality in this patient population is mostly cancer-related, we believe that the influences of such comorbidities on outcome would be minimal.

The diabetic patients with proper glycemic control exhibited better OS than the diabetic patients without proper glycemic control and even exhibited better OS than did the patients without diabetes mellitus. Metformin use was independently associated with improved OS.

The use of metformin and the achievement of proper glycemic control have beneficial effects on the survival of patients with diabetes and advanced NSCLC. Prospective clinical trials of the use of metformin for lung cancer should be performed, particularly in selected populations in which the effects of metformin on signaling pathways could be potentially beneficial.

ADA, American Diabetes Association; AMPK, AMP-activated protein kinase; CI, confidence interval; EGFR, epidermal growth factor receptor; HbA1C, glycated hemoglobin; INCan, Instituto Nacional de Cancerología (Mexico City, Mexico); LKB1, liver kinase 1; NSCLC, Non-small cell lung cancer; OS, overall survival; SD, standard deviations