Footnotes No potential conflict of interest.
Gastric cancer is one of the most prevalent cancers worldwide and is a leading cause of cancer mortality. In several Eastern countries, gastric cancer is the most common and deadly malignancy. In the Western Hemisphere gastric cancer incidence has been decreasing while esophageal and gastroesophageal

junction cancers have increased (1),(2). In Inhibitors,research,lifescience,medical the West, gastric cancers are typically distributed in the proximal lesser curvature, in the cardia, and in the GE junction; this distribution has been changing from a more distal distribution in the past and differs from Eastern countries with higher incidence. More than 80% of gastric cancer patients in the West are diagnosed at an advanced stage resulting in poor prognosis (3). Complete resection of gastric cancer is the only method of achieving permanent control. However, surgeries can be Inhibitors,research,lifescience,medical morbid and futile in patients who have advanced disease, making appropriate staging and characterization of disease burden of paramount importance. Staging of gastric cancer typically makes use of a variety of imaging modalities,

Inhibitors,research,lifescience,medical such as computed tomography (CT), magnetic resonance imaging (MRI), endoscopic ultrasounds (EUS), and combined positron tomography (PET-CT), as well as laparoscopic staging and cytogenetic analysis of peritoneal fluid in appropriate patients (4)-(6). The value of PET-CT has been of increasing interest among clinicians and data has supported its increased use in the detection, staging, and management of a variety of malignancies. During and after therapy, PET-CT may be useful in determining response to chemotherapy. It may be helpful for restaging and diagnosing recurrence at an earlier time or with greater certainty. This paper Inhibitors,research,lifescience,medical will address the potential uses

of PET-CT specifically within the management of gastric cancer. Background PET Inhibitors,research,lifescience,medical is performed by injecting a patient with a selleckbio radio-labeled tracer which is concentrated by the body in certain metabolically active tissues. As radioactive decay occurs, emissions are measured GSK-3 with a scanner and a three-dimensional image representing relative uptake of the tracer is produced. 2-[fluorine 18] fluoro-2-deoxy-D-glucose (FDG) labeled glucose is used most frequently as the tracer, and this paper will assume the use of FDG unless otherwise indicated. As fluorine-labeled glucose is transported into metabolically active cells, it is phosphorylated and trapped, ensuring that continued dissipation and transport do not dilute the signal. These e-book biochemical properties make FDG-PET a useful modality for measuring glucose demand as a surrogate for metabolically active tissues such as cancer. In several gastric cancer histologies, however, the metabolic differential between tumor and normal tissue is not as stark as with other malignancies, making the conceptual utility of PET less clear.