Efficacy of metformin for advanced-stage endometrial cancer: A case report

Introduction

Endometrial cancer (EC) is the third most common gynecological malignancy worldwide, after breast and cervical cancers (1). While insulin resistance and diabetes mellitus (DM) may facilitate the initiation and progression of EC, effective DM control has been suggested to prevent or modulate EC (2). Metformin is an oral insulin-sensitizing agent used as first-line therapy for type 2 DM (3). As shown in a recent review, several in vitro and observational studies have evaluated the potential benefits of metformin in the prevention or treatment of gynecological cancers (4,5). In vitro data have demonstrated that metformin administration inhibits the growth and decreases the invasion and metastasis of EC cell lines (6,7). A multi-institutional study recently demonstrated that metformin use was associated with an improvement in the recurrence-free and overall survival of patients with EC (8). We herein describe the case of a patient with EC who was treated with metformin and remained disease-free during a long follow-up period.

Case report

A 79-year-old woman, gravida 1, para 0, presented with lower abdominal pain. The patient was examined in a gynecological clinic (September, 2012). Magnetic resonance imaging (MRI) revealed a mass sized ~4 cm in the endometrium (Fig. 1) and computed tomography (CT) revealed two 2-cm peritoneal disseminations (Fig. 2). The carbohydrate antigen-125 level was 53 ng/ml (normal range, <35 ng/ml), and the carcinoembryonic antigen level was 8.6 ng/ml (normal range, <5.0 ng/ml). The diagnosis was endometrial adenocarcinoma. The patient had a history of type 2 DM and hypertension, but was not obese (body mass index, 23.6 kg/m2). The HbA1c level (National Glycohemoglobin Standardization Program) was 9.1%, and the patient was treated with oral medications [sulfonylurea and dipeptidyl peptidase-4 (DPP-4) inhibitor].

Figure 1. Magnetic resonance image showing the endometrial cancer. Preoperative T2-weighted images: (A) sagittal section and (B) horizontal section

Figure 2. Computed tomographic images showing peritoneal dissemination. (A) Dorsal side of the transverse colon and (B) anterior side of the left kidney.

The patient was referred to the Shimane University Hospital for treatment of the pelvic and abdominal masses, where she underwent modified radical hysterectomy, bilateral salpingo-oophorectomy, pelvic lymphadenectomy and abdominal mass resection. All identifiable masses were resected. Pathological examination revealed a stage IVB (International Federation of Gynecology and Obstetrics 2008), pT1aN0M1 endometrial serous adenocarcinoma.

Although adjuvant chemotherapy was planned, the postoperative follow-up was complicated by perforation of the digestive tract and severe inflammation of the peritoneum. To control glycemia, insulin was initially used, but it was replaced with metformin (250 mg once a day) and other oral medications (sulfonylurea and DPP-4 inhibitor) following discharge from the hospital. No further medical treatment was performed.

After being discharged from the hospital, the patient did not exhibit elevated levels of tumor markers or any metastases on CT. At 45 months after the initial metformin treatment, the patient had no complaints and maintained a good quality of life, without signs of tumor progression.

Discussion

The mechanism underlying the antitumor effect of metformin is considered to involve the activation of adenosine monophosphate-activated protein kinase and inhibition of the mammalian target of rapamycin, which reduces cell growth (9). Metformin arrests the cell cycle of EC cells, decreases human telomerase reverse transcriptase mRNA expression, and inhibits the phosphorylation of S6RP, resulting in the inhibition of signaling downstream of the mRNA pathway (10,11). Thus, in EC, cell cycle arrest by metformin has been observed in vitro, and inhibition of telomerase activity may be an important mechanism underlying the antitumor activity of this drug (10).

Clinical evidence on the effect of metformin on EC outcome is limited to retrospective data and does not generally account for the effects of multiple covariates, such as pathology, stage and treatment, on clinical outcome (12). It cannot be definitively concluded that patients who receive metformin are less likely to succumb to EC, as metformin may also reduce mortality from other causes (e.g., complications of diabetes and cardiovascular disease) (13).

In the present case, adjuvant chemotherapy and radiotherapy could not be administered, but the patient remained disease-free over a long period of time with metformin therapy alone. The contribution of complete surgical resection to this clinical benefit cannot be ruled out. Moreover, whether this was the natural course of EC in our patient remains unclear. Despite these limitations, this clinical case suggests that metformin is potentially beneficial in the prevention or treatment of EC. This finding deserves further validation in clinical studies (14–16).

References