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Ok<strong>an</strong>o K et al . FDG-PET small p<strong>an</strong>creatic c<strong>an</strong>cer diagnosis<br />

approximates the <strong>an</strong>nual incidence, thereby reflecting a<br />

generally short survival time <strong>as</strong>sociated with p<strong>an</strong>creatic<br />

c<strong>an</strong>cer, which is generally less th<strong>an</strong> 1 year. C<strong>an</strong>cer <strong>of</strong> the<br />

p<strong>an</strong>cre<strong>as</strong> h<strong>as</strong> the shortest medi<strong>an</strong> survival time out <strong>of</strong> all<br />

c<strong>an</strong>cer types in a stage for stage b<strong>as</strong>is. Early diagnosis is<br />

the most import<strong>an</strong>t <strong>factor</strong> for improving the overall survival<br />

<strong>an</strong>d quality <strong>of</strong> life in patients with p<strong>an</strong>creatic c<strong>an</strong>cer.<br />

Recently, positron emission tomography (PET) h<strong>as</strong><br />

demonstrated superiority to computed tomography (CT),<br />

ultr<strong>as</strong>onography (US), <strong>an</strong>d endoscopic US (EUS) in its<br />

sensitivity <strong>an</strong>d specificity in diagnosing p<strong>an</strong>creatic c<strong>an</strong>cer<br />

[3-6] . Furthermore, the metabolic activity <strong>of</strong> the tumor<br />

may be <strong>of</strong> prognostic signific<strong>an</strong>ce. We have been reported<br />

the efficacy <strong>of</strong> delayed additional 18 F-fluorodeoxyglucose<br />

PET (FDG-PET) imaging in the differential diagnosis<br />

<strong>of</strong> malign<strong>an</strong>t from benign lesions in patients who are<br />

suspected <strong>of</strong> having p<strong>an</strong>creatic c<strong>an</strong>cer [7] . Furthermore,<br />

the detection rate <strong>of</strong> liver met<strong>as</strong>t<strong>as</strong>es smaller th<strong>an</strong> 1 cm in<br />

diameter from p<strong>an</strong>creatic c<strong>an</strong>cer w<strong>as</strong> only 33% on early<br />

image <strong>an</strong>d 58% on delayed image [7] . However, the role <strong>of</strong><br />

dual time point FDG-PET in the diagnosis <strong>of</strong> small p<strong>an</strong>creatic<br />

c<strong>an</strong>cers h<strong>as</strong> yet to be established.<br />

Therefore, the present study investigated whether<br />

small c<strong>an</strong>cers <strong>of</strong> the p<strong>an</strong>cre<strong>as</strong> could be accurately diagnosed<br />

by FDG-PET with dual time point evaluation.<br />

MATERIALS AND METHODS<br />

Patients<br />

Thirty-one patients with p<strong>an</strong>creatic carcinoma suspected<br />

on the b<strong>as</strong>is <strong>of</strong> conventional radiological studies (22 males<br />

<strong>an</strong>d 9 females; me<strong>an</strong> age, 65 years; age r<strong>an</strong>ge, 44-82 years)<br />

<strong>an</strong>d who underwent FDG-PET between 2003 <strong>an</strong>d 2007<br />

were retrospectively selected. Patients were excluded from<br />

this study if they had poorly controlled diabetes mellitus<br />

(presenting with blood glucose level > 200 mg/dL<br />

prior to PET imaging). Conventional radiological staging<br />

w<strong>as</strong> performed by me<strong>an</strong>s <strong>of</strong> CT or magnetic reson<strong>an</strong>ce<br />

imaging (MRI). The location <strong>of</strong> the c<strong>an</strong>cer w<strong>as</strong> in<br />

the head <strong>of</strong> the p<strong>an</strong>cre<strong>as</strong> in 17 patients <strong>an</strong>d in the body<br />

<strong>an</strong>d tail in 14 patients. Twelve <strong>of</strong> the 31 c<strong>an</strong>cers were<br />

diagnosed to be unresectable, <strong>an</strong>d 19 patients eventually<br />

underwent surgery with a curative intention, although the<br />

c<strong>an</strong>cer turned out to be unresectable in 7 because <strong>of</strong> intraoperative<br />

findings.<br />

Methods<br />

The patients were divided into 3 groups according to the<br />

maximum diameter <strong>of</strong> the tumor: TS1 (maximum size ≤<br />

2.0 cm), TS2 (> 2.0 cm <strong>an</strong>d ≤ 4.0 cm) or TS3-4 (> 4.0 cm)<br />

<strong>as</strong> indicated by the cl<strong>as</strong>sification system <strong>of</strong> the Jap<strong>an</strong><br />

P<strong>an</strong>cre<strong>as</strong> Society. FDG-PET w<strong>as</strong> <strong>an</strong>alyzed semi-qu<strong>an</strong>titatively<br />

using the st<strong>an</strong>dardized uptake values (SUVs). The<br />

sensitivity <strong>of</strong> diagnosing p<strong>an</strong>creatic c<strong>an</strong>cer w<strong>as</strong> examined<br />

for FDG-PET, CT, MRI <strong>an</strong>d the serum levels <strong>of</strong> carcinoembryonic<br />

<strong>an</strong>tigen (CEA) <strong>an</strong>d carbohydrate <strong>an</strong>tigen<br />

19-9 (CA19-9) with regard to the size <strong>of</strong> the tumor. The<br />

details <strong>of</strong> SUVs, the histological findings <strong>an</strong>d correlation<br />

<strong>of</strong> CT findings were evaluated in patients with TS1 p<strong>an</strong>-<br />

WJG|www.wjgnet.com<br />

creatic c<strong>an</strong>cer. This study w<strong>as</strong> performed retrospectively<br />

by collecting <strong>an</strong>d <strong>an</strong>alyzing data from the patient records.<br />

FDG-PET<br />

The FDG-PET images were acquired with a PET machine<br />

(Siemens EXACT HR+, CTI, Knoxville, TN, USA).<br />

The patients were required to f<strong>as</strong>t for at le<strong>as</strong>t 4 h before<br />

PET imaging. The emission images were acquired (early<br />

image) 1 h after the intravenous administration <strong>of</strong> 5 mCi<br />

<strong>of</strong> FDG. Delayed PET emission images <strong>of</strong> the upper<br />

abdomen were acquired at 2 h after administration <strong>of</strong> 18 F-<br />

FDG, using 2 or 3 bed positions with a 3-min acquisition<br />

at each [7] . This acquisition w<strong>as</strong> immediately followed by<br />

a tr<strong>an</strong>smission sc<strong>an</strong> <strong>of</strong> the same tr<strong>an</strong>sverse pl<strong>an</strong>es, using<br />

a 2-min acquisition at each bed position. The early <strong>an</strong>d<br />

delayed PET images were reviewed independently <strong>an</strong>d<br />

consecutively by 2 radiologists with extensive experience<br />

in FDG-PET imaging. PET images were compared with<br />

the corresponding CT <strong>an</strong>d/or MRI images for accurate<br />

<strong>an</strong>atomical identification <strong>of</strong> the tumor. The findings were<br />

considered to be positive when both radiologists strongly<br />

suspected malign<strong>an</strong>t dise<strong>as</strong>e. In addition, the images were<br />

<strong>an</strong>alyzed semi-qu<strong>an</strong>titatively using the SUV, <strong>as</strong> reported<br />

elsewhere. Briefly, for semi-qu<strong>an</strong>titative <strong>an</strong>alysis, a region<br />

<strong>of</strong> interest w<strong>as</strong> placed over the entire FDG-avid lesion<br />

including the largest amount <strong>of</strong> radioactivity using the<br />

tr<strong>an</strong>sverse PET image. The SUV w<strong>as</strong> calculated <strong>as</strong>: SUV<br />

= (activity in region <strong>of</strong> interest in mCi)/(injected dose in<br />

mCi/weight in kg).<br />

CT<br />

CT studies were performed with a multidetector row CT<br />

sc<strong>an</strong>ner (Aquilion, Toshiba, Tokyo, Jap<strong>an</strong>). Helical images<br />

<strong>of</strong> the abdomen were routinely obtained <strong>an</strong>d reconstructed<br />

with 5 mm thickness. After pre-contr<strong>as</strong>t CT sc<strong>an</strong>s, arterial<br />

domin<strong>an</strong>t ph<strong>as</strong>e images <strong>of</strong> dynamic CT were obtained<br />

starting 40 s after the beginning <strong>of</strong> the intravenous bolus<br />

injection (3 mL/s) <strong>of</strong> 100 mL <strong>of</strong> iodized contr<strong>as</strong>t medium<br />

at 350 mg/mL. The p<strong>an</strong>creatic ph<strong>as</strong>e <strong>an</strong>d the late ph<strong>as</strong>e<br />

(near equilibrium ph<strong>as</strong>e) were also obtained, starting at<br />

60 <strong>an</strong>d 180 s after injection, respectively. The CT images<br />

were interpreted independently <strong>an</strong>d consecutively by 2 radiologists<br />

with extensive experience <strong>of</strong> more th<strong>an</strong> 10 years<br />

in CT sc<strong>an</strong>ning. The findings <strong>of</strong> the CT sc<strong>an</strong>s were considered<br />

positive when both radiologists strongly suspected<br />

malign<strong>an</strong>t dise<strong>as</strong>e due to a discrete low-attenuation m<strong>as</strong>s<br />

within the p<strong>an</strong>cre<strong>as</strong>.<br />

MRI<br />

Two 1.5 T superconducting units, Signa Adv<strong>an</strong>tage (General<br />

Electric, Milwaukee, WI, USA, USA) <strong>an</strong>d Visart<br />

(Toshiba, Tokyo, Jap<strong>an</strong>), were used for MRI. T1-weighted<br />

gradient-echo imaging; FS-T2-weighted turbo SE imaging<br />

<strong>an</strong>d heavily T2-weighted turbo SE images were acquired in<br />

the order <strong>of</strong> sc<strong>an</strong> after initial T1-weighted localizing images<br />

were obtained in the coronal <strong>an</strong>d tr<strong>an</strong>s-axial directions.<br />

Statistical <strong>an</strong>alysis<br />

The χ 2 test w<strong>as</strong> employed for a statistical comparison <strong>of</strong><br />

232 J<strong>an</strong>uary 14, 2011|Volume 17|Issue 2|

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