Peer-review started: November 9, 2014
First decision: December 12, 2014
Revised: January 15, 2015
Accepted: February 4, 2015
Article in press: February 9, 2015
Published online: March 28, 2015
Processing time: 136 Days and 23 Hours
Metformin is the most widely used hypoglycemic agent. Besides its conventional indications, increasing evidence demonstrate a potential efficacy of this biguanide as an anticancer drug. Possible mechanisms of actions seem to be independent from its hypoglycemic effect and seem to involve the interference with key pathways in cellular proliferation and glycolysis. To date, many clinical trials implying the use of metformin in cancer treatment are on-going. The increasing use of 18F-2-fluoro-2-deoxy-d-glucose positron emission tomography (FDG-PET) in cancer evaluation raises a number of questions about the possible interference of the biguanide on FDG distribution. In particular, the interferences exerted by metformin on AMP-activated protein kinase pathway (the cellular energy sensor), on insulin levels and on Hexokinase could potentially have repercussion on glucose handling and thus on FDG distribution. A better comprehension of the impact of metformin on FDG uptake is needed in order to optimize the use of PET in this setting. This evaluation would be useful to ameliorate scans interpretation in diabetic patients under chronic metformin treatment and to critically interpret images in the context of clinical trials. Furthermore, collecting prospective data in this setting would help to verify whether FDG-PET could be a valid tool to appreciate the anticancer effect of this new therapeutic approach.
Core tip: Given the recent increasing number of clinical trials involving the use of metformin as anticancer agent and with the widespread use of 18F-2-fluoro-2-deoxy-d-glucose positron emission tomography (FDG-PET), this editorial deals with a critical evaluation of the main variables regulating FDG uptake that could be potentially influenced by the biguanide. This analysis could optimize not only the interpretation of PET images in diabetic patients but could also help to verify whether FDG-PET could be a valid tool to appreciate anticancer potential of this new therapeutic approach thus opening a new window on clinical trials.