- Research article
- Open Access
- Open Peer Review
The role of PET/CT in detection of gastric cancer recurrence
© Sim et al; licensee BioMed Central Ltd. 2009
- Received: 18 August 2008
- Accepted: 01 March 2009
- Published: 01 March 2009
In the course of surveillance of gastric cancer recurrence after curative resection, contrast CT scan is used in general. However, new findings from CT scan are not always confirmatory for the recurrence. In this case, we usually use short-term follow up strategy or therapeutic intervention with clinical decision. Recently, the use of fusion Positron Emission Tomography/Computed Tomography (PET/CT) is increasing. The purpose of this study is to evaluate the efficacy and usefulness of PET/CT for detecting recurrence of gastric cancer after curative resection.
Fifty two patients who received curative resection of gastric cancer and had undergone PET/CT and contrast CT for surveillance of recurrence until Dec 2006 in Seoul National University Hospital were analyzed retrospectively. Recurrence of gastric cancer was validated by histologic confirmation (n = 17) or serial contrast CT follow up with at least 5 month interval (n = 35). McNemar's test and Fisher's exact test were used to evaluate sensitivity and specificity of PET/CT and contrast CT.
Of 52 patients, 38 patients were confirmed as recurrence. The sensitivity was 68.4% (26/38) for PET/CT and 89.4% (34/38) for contrast CT (p = 0.057). The specificity was 71.4% (10/14) and 64.2% (9/14), respectively (p = 1.0). In terms of the recurred sites, the sensitivity and specificity of PET/CT were similar to those of contrast CT in all sites except peritoneum. Contrast CT was more sensitive than PET/CT (p = 0.039) for detecting peritoneal seeding. Additional PET/CT on contrast CT showed no further increase of positive predictive value regardless of sites. Among 13 patients whose image findings between two methods were discordant and tissue confirmation was difficult, the treatment decision was made in 7 patients based on PET/CT, showing the final diagnostic accuracy of 42.8% (3/7).
PET/CT was as sensitive and specific as contrast CT in detection of recurred gastric cancer except peritoneal seeding. However, additional PET/CT on contrast CT did not increase diagnostic accuracy in detection of recurred gastric cancer. Further studies are warranted to validate the role of PET/CT in detection of gastric cancer recurrence.
- Gastric Cancer
- Positron Emission Tomography
- Curative Resection
- Peritoneal Carcinomatosis
- Gastric Cancer Recurrence
Gastric cancer is the fourth most common cancer worldwide with approximately 930,000 new cases and 700,000 deaths per year . The incidence of stomach cancer is high in Asia, and it is the most common cancer in Korea .
Early gastric cancer can be cured by complete resection, while advanced disease often recurs in 40~60% of patients after surgery [3, 4]. To detect cancer recurrence, various methods such as tumor markers, endoscopy or imaging studies have been used. However, tumor markers cannot localize the recurrence site and endoscopy cannot detect extra-luminal recurrence .
At present, the most frequently used method for the detection of gastric cancer recurrence is contrast-enhanced computed tomography (contrast CT) [5, 6]. However, CT has a notable limitation on diagnosis of malignancy because it uses the size criteria. Therefore, it cannot reflect the presence and viability of tumor precisely.
Fluorine 18 (18F) fluorodeoxyglucose (FDG) positron emission tomography (PET), in contrast with CT, is a tool that reflects cancer metabolism and cell biology. Recently, FDG-PET combined with CT (Fusion PET/CT) has been introduced and is expected to give us more precise anatomical data with metabolic information. Fusion PET/CT has been reported to be useful for staging of lung, colorectal, breast, lymphoma, head and neck cancer and for detecting recurrence of lung, colorectal, thyroid, and breast cancer [7–14]. However, in contrast to the other cancer, it has been reported that FDG uptake of gastric cancer cell is relatively poor and the PET image has a limitation on the detection of recurred gastric cancer [15, 16].
The definitive method for diagnosis of gastric cancer recurrence is the pathologic confirmation. However, getting adequate tissues is often difficult because either recurred tumor size is very small or it is deeply located or too close to great vessels or organs for needle biopsy.
In clinical practice, it is hard to make treatment decision when gastric cancer recurrence is suspicious in contrast CT but tissue confirmation is difficult. In this case, additional PET/CT could give us more information on the detection of recurrence. Therefore, we conducted this study to evaluate efficacy and usefulness of PET/CT for the detection and confirmation of recurred gastric cancer after curative resection.
All information was collected and analyzed retrospectively. We screened all the patients with gastric cancer who received curative resection and had subsequently undergone contrast CT and PET/CT for the surveillance of recurrence between Apr. 2004 and Dec. 2006 in Seoul National University Hospital. The patients were enrolled when the cancer recurrence can be validated by tissue confirmation or by the change of lesions on contrast CT follow up of at least 5-month interval. Basically, all the patients had undergone routine follow up with 3 to 6 month interval after curative resection. Regardless of PET/CT, the diagnostic contrast CT scan was performed with 120 kVP, 120 mA, 5 mm thickness and 90 ml contrast media, which were adjusted to body weight.
All scans were performed by PET/CT system (Philips Gemini, DA best, Netherlands). The patients were asked to fast for at least 4 hours before undergoing PET/CT and 555–740 MBq (15–20 mCi; 0.22 mCi/kg body weight) of FDG was administered intravenously 1 hour prior to imaging. CT was performed prior to PET, and the resulting data were used to generate an attenuation correction map for PET. Five-millimeter-thick sections were obtained at 50 mA (but adjusted for body thickness) and 120 kVp from the skull base to the mid-thigh. Next, PET was performed with a 5-min emission acquisition per imaging level and the images were reconstructed.
Data analysis and Statistical methods
Fusion PET/CT was reviewed by a nuclear medicine physician who was aware of patients' information on clinical findings and other imaging results. All lesions in PET/CT and contrast CT were categorized as suspicious, negative or equivocal lesions. Exo and Endo luminal recurrence was categorized as locoregional recurrence and the other patents of recurrence categorized as metastasis. In statistical analysis, the equivocal lesions were considered as negative lesions. Recurrence of gastric cancer was validated by histologic confirmation or serial contrast CT follow up. It was regarded as negative lesion when there was no change between CT images of at least the 5 month interval. Overall and site-specific sensitivity, specificity, positive and negative predictive values were calculated. McNemar's test and Fisher's exact test were used to evaluate the efficacy of PET/CT and contrast CT.
The study protocol was reviewed and approved by the institutional review board of Seoul National University Hospital. The recommendations of the Declaration of Helsinki for biomedical research involving human subjects were also followed.
signet ring cell type
Interval between CT and PET/CT
Detection of Recurrence by fusion PET/CT and contrast CT
Recurrence and its specific site
Clinical confirmation by image
(Remnant stomach or anastomosis site)
Other site (bone, skin, etc.)
Fusion PET/CT in addition to contrast CT
Overall and site specific sensitivity and specificity of contrast CT and fusion PET/CT
Remnant stomach or anastomosis site
Positive predictive value of contrast CT alone and of combination of the two methods
PPV(%) in Contrast CT +*
PPV(%) in Fusion PETCT +* and contrast CT +*
Remnant stomach or anastomosis
Age and stage distribution in patients with discordant findings but no tissue confirmation
Age(mean ± SD)
57.0 ± 15.4
62.8 ± 11.1
Our study showed that PET/CT was as sensitive and specific as contrast CT in the detection of gastric cancer recurrence except in peritoneal carcinomatosis. Despite this result, additional PET/CT on contrast CT did not give us more accurate information to confirm cancer recurrence.
There are some reports about the role of FDG-PET or fusion PET/CT in the evaluation of gastric cancer recurrence after curative resection, but the results are inconsistent. Jadvar, et al. reports that FDG PET might be useful in the post-therapy evaluation of recurrent disease. Park, et al. also suggested that PET/CT might have a role for detecting recurrence in post-operative patients with gastric cancer. On the other hand, De Potter, et al. reported that FDG-PET might not be suitable as a primary tool for follow up due to its moderate accuracy.
In the aspect of sensitivity, fusion PET/CT alone was as sensitive as contrast CT in most recurred sites according to our study. However, the statistical significance is marginal (p = 0.057) and the sensitivity of PET/CT showed inferior tendency compared to contrast CT. Moreover, PET/CT was inferior to contrast CT for detection of peritoneal recurrence, which corresponds with other previous reports [10, 20].
These might be attributed to the method of CT validation that could make the ability of contrast CT overestimated. The other explanation would be due to the low metabolic activity of recurred gastric cancer. The interpretation of PET/CT is on both metabolic status of lesion and its anatomical location on non-contrast CT. It is well known FDG avidity depends on histologic type . Signet ring cell type or mucinous type is known to have low FDG avidity. However, only a small portion of signet ring cell cancer patients was included in the study population. And the FDG avidity has not been known yet in recurred gastric cancer.
In the aspect of the confirmation of recurrence, the benefits of additional PET/CT on contast CT were low. This may be because either additional PET/CT has little benefit on prediction of gastric cancer recurrence or the study population is too small to reveal the substantial benefits. However, considering its high cost and small benefits, the usefulness of additional PET/CT on contrast CT is unsatisfactory.
Some reports showed that clinical information including age, tumor size, histologic type, the number of involved LN could be the risk factors for gastric cancer recurrence[21, 22]. Our study also showed similar results of increasing tendency of recurrence in higher stages regardless of results of fusion PET/CT (Table 5). Therefore, clinical factors such pathological stage could be more helpful to making treatment decision than PET/CT findings.
Our study has a few limitations. First, not all the recurred cases were confirmed by pathologic diagnosis. the validation of recurrence by contrast CT may have caused physicians to overestimate the detection rate of contrast CT. In addition, 5-month interval may not be enough time to confirm the absence of recurrence. Second, it is a retrospective study with small study population. In our data, although about a half of total patients was early stage patients, the recurrence rate was extremely high. However, although the possibility of selection bas, recurrence to non-recurrence ratio showed the increasing trend of recurrence rate as the stage get advanced in the patients with discordant findings (Table 5).
Despite these deficiencies, our study has significance in giving us evidence of the role of fusion PET/CT in post operative surveillance and in the clinical decision-making process. Further prospective studies enrolling large populations are needed to establish the role of fusion PET/CT in detection of gastric cancer recurrence.
In conclusion, the role of fusion PET/CT in detection and confirmation of recurrence of gastric cancer is limited. Further well-designed prospective study is needed to establish the role of fusion PET/CT in detection of gastric cancer recurrence
This study was supported by a grant (A080316) of the Korea Healthcare technology R&D Project, Ministry for Health, Welfare & Family Affairs, Republic of Korea.
- Ferlay J, Bray F, Pisani P, Parkin DM: GLOBOCAN 2002, Cancer Incidence, Mortality and Prevalence Worldwide. 2004, IARC CancerBase No 5, version 20 IARCPress, LyonGoogle Scholar
- Ministry of Health and Welfare: Ministry of Health and Welfare 2002 Annual Report of the Korea Central Cancer Registry. 2003Google Scholar
- Macdonald JS, Smalley SR, Benedetti J, Hundahl SA, Estes NC, Stemmermann GN, Haller DG, Ajani JA, Gunderson LL, Jessup JM, et al: Chemoradiotherapy after surgery compared with surgery alone for adenocarcinoma of the stomach or gastroesophageal junction. The New England journal of medicine. 2001, 345 (10): 725-30. 10.1056/NEJMoa010187.View ArticlePubMedGoogle Scholar
- Wu CW, Lo SS, Shen KH, Hsieh MC, Chen JH, Chiang JH, Lin HJ, Li AF, Lui WY: Incidence and factors associated with recurrence patterns after intended curative surgery for gastric cancer. World journal of surgery. 2003, 27 (2): 153-8.PubMedGoogle Scholar
- Whiting J, Sano T, Saka M, Fukagawa T, Katai H, Sasako M: Follow-up of gastric cancer: a review. Gastric Cancer. 2006, 9 (2): 74-81. 10.1007/s10120-006-0360-0.View ArticlePubMedGoogle Scholar
- Kim KW, Choi BI, Han JK, Kim TK, Kim AY, Lee HJ, Kim YH, Choi JI, Do KH, Kim HC, et al: Postoperative anatomic and pathologic findings at CT following gastrectomy. Radiographics. 2002, 22 (2): 323-36.View ArticlePubMedGoogle Scholar
- Gamez C, Rosell R, Fernandez A, Andia E, Arnaiz MD, Cardenal F, Lorenzo C: PET/CT fusion scan in lung cancer: current recommendations and innovations. J Thorac Oncol. 2006, 1 (1): 74-7.View ArticlePubMedGoogle Scholar
- Chen LB, Tong JL, Song HZ, Zhu H, Wang YC: (18)F-DG PET/CT in detection of recurrence and metastasis of colorectal cancer. World J Gastroenterol. 2007, 13 (37): 5025-9.View ArticlePubMedPubMed CentralGoogle Scholar
- Even-Sapir E, Parag Y, Lerman H, Gutman M, Levine C, Rabau M, Figer A, Metser U: Detection of recurrence in patients with rectal cancer: PET/CT after abdominoperineal or anterior resection. Radiology. 2004, 232 (3): 815-22. 10.1148/radiol.2323031065.View ArticlePubMedGoogle Scholar
- Yoshioka T, Yamaguchi K, Kubota K, Saginoya T, Yamazaki T, Ido T, Yamaura G, Takahashi H, Fukuda H, Kanamaru R: Evaluation of 18F-FDG PET in patients with a, metastatic, or recurrent gastric cancer. J Nucl Med. 2003, 44 (5): 690-9.PubMedGoogle Scholar
- Schoder H, Yeung HW, Gonen M, Kraus D, Larson SM: Head and neck cancer: clinical usefulness and accuracy of PET/CT image fusion. Radiology. 2004, 231 (1): 65-72. 10.1148/radiol.2311030271.View ArticlePubMedGoogle Scholar
- Freudenberg LS, Antoch G, Schutt P, Beyer T, Jentzen W, Muller SP, Gorges R, Nowrousian MR, Bockisch A, Debatin JF: FDG-PET/CT in re-staging of patients with lymphoma. European journal of nuclear medicine and molecular imaging. 2004, 31 (3): 325-9. 10.1007/s00259-003-1375-y.View ArticlePubMedGoogle Scholar
- Finkelstein SE, Grigsby PW, Siegel BA, Dehdashti F, Moley JF, Hall BL: Combined [(18)F]Fluorodeoxyglucose Positron Emission Tomography and Computed Tomography (FDG-PET/CT) for Detection of Recurrent, (131)I-Negative Thyroid Cancer. Ann Surg Oncol. 2008, 15 (1): 286-92. 10.1245/s10434-007-9611-5.View ArticlePubMedGoogle Scholar
- Veit-Haibach P, Luczak C, Wanke I, Fischer M, Egelhof T, Beyer T, Dahmen G, Bockisch A, Rosenbaum S, Antoch G: TNM staging with FDG-PET/CT in patients with primary head and neck cancer. European journal of nuclear medicine and molecular imaging. 2007, 34 (12): 1953-62. 10.1007/s00259-007-0564-5.View ArticlePubMedGoogle Scholar
- Stahl A, Ott K, Weber WA, Becker K, Link T, Siewert JR, Schwaiger M, Fink U: FDG PET imaging of locally advanced gastric carcinomas: correlation with endoscopic and histopathological findings. European journal of nuclear medicine and molecular imaging. 2003, 30 (2): 288-95.View ArticlePubMedGoogle Scholar
- Mochiki E, Kuwano H, Katoh H, Asao T, Oriuchi N, Endo K: Evaluation of 18F-2-deoxy-2-fluoro-D-glucose positron emission tomography for gastric cancer. World journal of surgery. 2004, 28 (3): 247-53. 10.1007/s00268-003-7191-5.View ArticlePubMedGoogle Scholar
- Jadvar H, Tatlidil R, Garcia AA, Conti PS: Evaluation of recurrent gastric malignancy with [F-18]-FDG positron emission tomography. Clinical radiology. 2003, 58 (3): 215-21. 10.1016/S0009-9260(02)00477-4.View ArticlePubMedGoogle Scholar
- Park MJ, Lee WJ, Lim HK, Park KW, Choi JY, Kim BT: Detecting recurrence of gastric cancer: the value of FDG PET/CT. Abdominal imaging. 2008, http://www.springerlink.com/content/27243342023246gw/fulltext.pdf, ,Google Scholar
- De Potter T, Flamen P, Van Cutsem E, Penninckx F, Filez L, Bormans G, Maes A, Mortelmans L: Whole-body PET with FDG for the diagnosis of recurrent gastric cancer. European journal of nuclear medicine and molecular imaging. 2002, 29 (4): 525-9. 10.1007/s00259-001-0743-8.View ArticlePubMedGoogle Scholar
- Lim JS, Kim MJ, Yun MJ, Oh YT, Kim JH, Hwang HS, Park MS, Cha SW, Lee JD, Noh SH, et al: Comparison of CT and 18F-FDG pet for detecting peritoneal metastasis on the preoperative evaluation for gastric carcinoma. Korean J Radiol. 2006, 7 (4): 249-56.View ArticlePubMedPubMed CentralGoogle Scholar
- Yoo CH, Noh SH, Shin DW, Choi SH, Min JS: Recurrence following curative resection for gastric carcinoma. The British journal of surgery. 2000, 87 (2): 236-42. 10.1046/j.1365-2168.2000.01360.x.View ArticlePubMedGoogle Scholar
- Marrelli D, Roviello F, De Stefano A, Fotia G, Giliberto C, Garosi L, Pinto E: Risk factors for liver metastases after curative surgical procedures for gastric cancer: a prospective study of 208 patients treated with surgical resection. Journal of the American College of Surgeons. 2004, 198 (1): 51-8. 10.1016/j.jamcollsurg.2003.08.013.View ArticlePubMedGoogle Scholar
- The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2407/9/73/prepub
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.