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Impact of maximum Standardized Uptake Value (SUVmax) evaluated by 18-Fluoro-2-deoxy-D-glucose positron emission tomography/computed tomography (18F-FDG-PET/CT) on survival for patients with advanced renal cell carcinoma: a preliminary report

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BMC Cancer201010:667

https://doi.org/10.1186/1471-2407-10-667

©  Namura et al; licensee BioMed Central Ltd. 2010

  • Received: 19 May 2010
  • Accepted: 3 December 2010
  • Published:
Open Peer Review reports

Abstract

Background

In this era of molecular targeting therapy when various systematic treatments can be selected, prognostic biomarkers are required for the purpose of risk-directed therapy selection. Numerous reports of various malignancies have revealed that 18-Fluoro-2-deoxy-D-glucose (18F-FDG) accumulation, as evaluated by positron emission tomography, can be used to predict the prognosis of patients. The purpose of this study was to evaluate the impact of the maximum standardized uptake value (SUVmax) from 18-fluoro-2-deoxy-D-glucose positron emission tomography/computed tomography (18F-FDG PET/CT) on survival for patients with advanced renal cell carcinoma (RCC).

Methods

A total of 26 patients with advanced or metastatic RCC were enrolled in this study. The FDG uptake of all RCC lesions diagnosed by conventional CT was evaluated by 18F-FDG PET/CT. The impact of SUVmax on patient survival was analyzed prospectively.

Results

FDG uptake was detected in 230 of 243 lesions (94.7%) excluding lung or liver metastases with diameters of less than 1 cm. The SUVmax of 26 patients ranged between 1.4 and 16.6 (mean 8.8 ± 4.0). The patients with RCC tumors showing high SUVmax demonstrated poor prognosis (P = 0.005 hazard ratio 1.326, 95% CI 1.089-1.614). The survival between patients with SUVmax equal to the mean of SUVmax, 8.8 or more and patients with SUVmax less than 8.8 were statistically different (P = 0.0012). This is the first report to evaluate the impact of SUVmax on advanced RCC patient survival. However, the number of patients and the follow-up period were still not extensive enough to settle this important question conclusively.

Conclusions

The survival of patients with advanced RCC can be predicted by evaluating their SUVmax using 18F-FDG-PET/CT. 18F-FDG-PET/CT has potency as an "imaging biomarker" to provide helpful information for the clinical decision-making.

Keywords

  • Renal Cell Carcinoma
  • Sorafenib
  • Sunitinib
  • Standardize Uptake Value
  • Metastatic Renal Cell Carcinoma

Background

Renal cell carcinoma (RCC) accounts for 3% of all adult cancers [1]. Approximately 30% of patients are diagnosed with metastases and an additional 20-40% of patients develop metastases after radical nephrectomy with curative intent [2, 3]. The outcome of patients with metastatic RCC is poor, with a median survival time of 10 to 21 months [4, 5]

Classical cytokine therapies have been the only systematic treatments available for advanced RCC for a long time [6–9]. The oncogenic mechanism of RCC has been elucidated and agents that target relevant biological pathways have been investigated. Multiple tyrosine kinase inhibitors (multiple TKIs) targeting vascular endothelial growth factor receptor (VEGFR) such as sunitinib and sorafenib have revolutionized the treatment of RCC [10, 11]. Although mammalian target of rapamycin (mTOR) inhibitor was not available in Japan at the time of this study, the efficacies of mTOR inhibitors have been reported [12, 13]. These developments have made it necessary to predict the prognosis of individual patients with advanced RCC and to select optimal management. Many clinical risk factors have been proposed, and classifications of patients using these risk factors have been established. The most common classification was proposed by the Memorial Sloan-Kettering Cancer Center group for cytokine-based therapies (MSKCC classification)[14], and modified criteria adapted for the new era of molecular targeting was reported recently and recommended in the National Comprehensive Cancer Network guideline (NCCN classification)[12, 15]. However, these classifications are not enough to determine the best treatment selection for an individual patient. Novel biomarkers to predict the prognosis of individual patients are therefore desired.

During the last decade, 18-fluoro-2-deoxy-D-glucose positron emission tomography (18F-FDG-PET) emerged as a useful non-invasive tool to evaluate the metabolic status of tumors. Numerous recent studies of various types of malignancies have reported an association between the 18F-FDG accumulation rate evaluated by PET and patient prognosis. The standardized uptake value (SUV) is a semiquantitative simplified measurement of the tissue FDG accumulation rate, and studies of the head-and-neck, lung, and cervical cancer have explored the prognostic significance of the maximum standardized uptake value (SUVmax) [16–19]. However, the role of the SUVmax as a prognostic factor for patients with advanced RCC has not yet been evaluated. In the present study, we evaluated prospectively the impact of SUVmax on the survival of patients with advanced RCC.

Methods

Patients

This was a prospective study to clinically follow enrolled patients planning to undergo systematic therapies for advanced RCC. In principle, the pathologies of enrolled cases were confirmed by prior nephrectomy or biopsy, but only one case was diagnosed clinically by conventional imaging because the patient wished to be treated immediately and did not consent to biopsy. The patients were initially assessed by conventional imaging techniques (computed tomography [CT], magnet resonance imaging [MRI], or bone scintigraphy) and diagnosed as stage IV or metastatic RCC. Patients with uncontrolled diabetes mellitus, with other known malignancies and treated with therapeutics the last 2 weeks before the scan were excluded.

The study protocol was approved by the Yokohama City University Institutional Review Board. Written informed consent was obtained from all patients. The patients underwent various therapeutic interventions decided before the evaluation by PET/CT at Yokohama City University Hospital and Kanagawa Cancer Center.

Imaging

Patients fasted for at least 6 hours prior to intravenous injection of [18F] FDG. PET/CT images were obtained using a PET/CT system (Aquiduo 16; Toshiba Medical Systems, Tokyo, Japan). PET/CT images were acquired from the top of the head to the mid thigh at 60 min after intravenous injection of 2.5 MBq/kg of [18F] FDG. A low-dose non-contrasted CT scan was acquired first and used for attenuation correction. Emission images were acquired in 3-dimensional mode for 2 min per bed position. After PET acquisition, CECT was performed with a 2-mm slice thickness, 120 kV, 400 mA, 0.5 s/tube rotation, from the top of the head to the mid thigh, with breath holding. A total of 100 ml contrast medium (iopamidol) was administered intravenously at a rate of 1.0 ml/s. The scan delay was set at 120 s after starting the injection of contrast material. Images were reconstructed by attenuation-weighted ordered-subset expectation maximization (OSEM) (four iterations, fourteen subsets, 128' 128 matrix, with 5-mm Gaussian smoothing). The highest SUV in all RCC tumors of each patient was defined as SUVmax. To obtain the SUVmax, the SUV values of all lesions in tumors diagnosed as RCC by CT imaging were analyzed.

Statistical analysis

Survival time was calculated from the date of evaluation by 18F-FDG PET/CT to the date of death. Cox proportional hazards model was used to assess the effects of SUVmax on survival. The cancer-specific survival curve was estimated by the Kaplan-Meier methods, and the resulting curves were compared using the log-rank test. All statistical analyses were carried out with SPSS software (SPSS, Inc, Chicago, IL).

Results

Patient characteristics and intervention

A total of 26 patients (21 males and 5 females) were enrolled in this study between 2008 Jun and 2009 October (Table 1). The median age was 61 years (range of 32-82). There were 17 patients with recurrent diseases and 9 with stage IV disease. Pathological examination showed 18 cases of clear cell carcinoma, 5 of papillary, and 2 of clear/sarcomatoid; in one case, the pathological type was unknown. As for prior surgeries, 19 patients had undergone nephrectomy and 4 metastatectomy. Thirteen patients had not undergone previous systematic therapies. Of the other 13 cases with previous systematic therapies, 9 patients had undergone interferon-alpha (IFN-α therapies, one sorafenib, one S1, one combined therapy with IFN-α and sorafenib, and one combined therapies with IFN-α and UFT.
Table 1

Characteristics of the 26 patients

Patient ID

Sex

Age

Pathology

Nephrectomy

MSKCC classification

NCCN classification

Prior therapy

SUVmax

SUVmax site

   

type

grading

      

2

M

63

sarc/clear

3

Yes

Poor

Poor

IFN

15.2

local recurrence

3

M

73

clear

2

Yes

Favorable

Not Poor

IFN IL

8.2

lung

4

M

61

papillary

3

No

Intermediate

Poor

non

8.8

primary

5

F

72

clear

1

No

Intermediate

Not Poor

non

5.2

primary

6

F

55

clear

2

No

Intermediate

Not Poor

IFN IL

6.8

primary

7

M

57

papillary

2

Yes

Intermediate

Poor

N

4.0

bone

8

M

59

clear

2

Yes

Intermediate

Poor

non

7.4

bone

9

M

68

clear

3

Yes

Intermediate

Not Poor

IFN

5.7

bone

10

F

57

clear

2

Yes

Poor

Poor

IFN N

9.1

lymph node

11

M

75

clear

2

Yes

Intermediate

Not Poor

IFN

5.3

muscle

12

M

58

clear

3

Yes

Favorable

Not Poor

IFN

8.5

local recurrence

13

F

61

clear

2

Yes

Intermediate

Poor

IFN C

4.3

pancreas

14

M

59

clear

2

Yes

Intermediate

Not Poor

non

1.4

lung

15

M

61

clear

2

Yes

Intermediate

Poor

IFN

7.7

lymph node

16

M

73

clear

2

No

Poor

Poor

non

16.6

primary

17

F

32

papillary

3

Yes

Favorable

Not Poor

non

16.1

uterus

18

M

56

papillary

2

Yes

Intermediate

Not Poor

C

7.0

lung

19

M

68

clear

2

Yes

Intermediate

Poor

non

9.0

bone

20

M

61

clear

2

Yes

Intermediate

Not Poor

non

5.6

IVC thrombus

21

F

56

sarc/clear

3

Yes

Intermediate

Poor

IFN

10.0

contralateral kidney

22

M

62

clear

3

No

Poor

Poor

non

12.0

primary

23

M

61

clear

3

No

Poor

Poor

non

14.3

primary

24

M

82

clear

1

Yes

Intermediate

Poor

non

5.1

bone

25

M

69

papillary

3

Yes

Favorable

Not Poor

non

13.4

lymph node

26

M

66

clear

1

Yes

Intermediate

Not Poor

IFN

8.2

lung

After the evaluation by PET/CT, 20 patients were treated with multiple TKIs (9 sorafenib, 9 sunitinib, 2 sequential therapy with sorafenib and sunitinib, and 1 sequential therapy with sorafenib and IFN-α), and 6 patients underwent cytokine therapies. At the follow-up end (January 2010), there were 9 cases with cancer death, and we confirmed the other 17 patients alive. There were no cases with death due to other causes and no cases dropped out during follow-up. The median follow-up period was 262 days (range, 43 to 531 days).

Accumulation of FDG in the lesions diagnosed as RCC tumor by CT imaging

We first, examined the FDG accumulation in all 368 tumor lesions in 26 patients who were diagnosed as stage IV or metastatic RCC by CT imaging. FDG uptake was detected in 230 of 243 lesions (94.7%) excluding lung or liver metastasis with diameters less than 1 cm. On the other hand, among 125 lung or liver lesions with diameters between 5 mm and 9 mm, FDG accumulations were detected in only 21 lesions (16.8%). The SUV in RCC lesions demonstrated various values from undetectable levels to 16.6. In 6 of 7 patients without prior nephrectomy, the primary tumor demonstrated the highest SUV in all RCC tumor lesions (Figure 1), and lung metastasis showed the highest SUV in another. In 19 cases with metastases or recurrence after nephrectomy, bone metastasis demonstrated the highest SUV in 5 cases, lung metastasis in 4 cases, lymph node metastases in 3 cases, and local recurrence in 2 cases (Figure 2). The uterus, pancreas, Inferior Vena Cava thrombus, muscle metastasis, and contra-lateral kidney metastasis demonstrated the highest SUV in one case each.
Figure 1
Figure 1

Four Cases with advanced RCC which original sites showed the highest value of SUV among all RCC sites and their prognosis. The patients with advanced RCCs having high values of SUV max demonstrated poor clinical courses. SUVmax, maximum standardized uptake value; CT, computed tomography; PET, positron emission tomography; Fused PET/CT, fusion of PET and CT.

Figure 2
Figure 2

Four Cases with advanced RCC which metastatic sites showed the highest value of SUV among all RCC sites and their prognosis. A cranial bone metastasis showed the highest SUV among all RCC sites in Patient 9. A metastasis in thoracic vertebra did in Patinet 19. Lung metastases did in Patient 1 and Patient 2. The patients with advanced RCCs having high values of SUV max demonstrated poor clinical courses. SUVmax, maximum standardized uptake value; CT, computed tomography; PET, positron emission tomography; Fused PET/CT, fusion of PET and CT.

The impact of SUVmax on patient survival time

We next analyzed the association between SUVmax and patient survival time. The SUVmax of all patients ranged between 1.4 and 16.6 (mean 8.8 ± 4.0). The patients with RCC tumors showing high SUVmax tended to demonstrate poor prognosis, as shown in Figure 1, 2, 3 (26 patients were lined up in order of SUVmax in Figure 3). When the patient population was subdivided using the mean SUVmax (8.8), only 2 (13%) of 15 patients with RCC tumors having an SUVmax less than 8.8 were dead due to cancer and the median survival time of the 15 patients was not calculated because the number of dead patients was less than half, whereas 7 (64%) of 11 patients RCC tumors having SUVmax equal to 8.8 or more and the median survival time of the 11 patients was 156 day (95% CI 33-279). The survival for these patient subgroups were significantly different (Figure 4) (P = 0.0012). When SUVmax was analyzed as a continuous variable, it was correlated with survival time (P = 0.005 hazard ratio 1.326 95% CI 1.089-1.614).
Figure 3
Figure 3

The treatments and prognoses of 26 patients lined up in order of SUVmax.

Figure 4
Figure 4

Survival curves of 26 patients that are stratified by SUVmax of 18 F-FDG-PET/CT.

Discussion

In the present study, we demonstrated that the SUVmax evaluated by 18F-FDG-PET/CT is a useful predictive "imaging biomarker" for survival of patients with advanced RCC. PET has not been generally used for the screening of RCC due to the urinary excretion of the radiotracer, which can mask the presence of primary lesions [20, 21]. However the large RCCs often presenting in stage IV could be evaluated without the influence of urinary excretion of the radiotracer by PET/CT providing combined morphological and functional information (Figure 1). In this study, 7 primary RCC lesions, with diameters ranging from 8.5 cm to 14.7 cm, were examined by 18F-FDG-PET/CT, and abnormal FDG accumulations sufficient to evaluate SUV were detected in all lesions. Pathological diagnosis was confirmed in 6 cases. Distant metastases of RCC could also be detected without interference of excretory radiotracers. We did not confirm the pathologies of the individual metastatic lesions, but the previous report by Majhail et al. warranted the accuracy of metastasis diagnosis by 18F-FDG-PET. They performed biopsy or surgical resection of 36 distant metastatic lesions in 24 patients that were diagnosed by 18F-FDG-PET, and pathological findings revealed metastatic RCC in 33 lesions (89%) [22]. In this study, FDG accumulation was evaluated in 94.9% of all RCC lesions diagnosed by CT scan except for lung or liver metastases less than 1 cm. These results were consistent with a previous report [23] and indicated that the information gained by 18F-FDG-PET/CT was sufficient to characterize advanced RCCs.

In this era of molecular targeting therapy when various systematic treatments can be selected, prognostic biomarkers are required for the purpose of risk-directed therapy selection. We revealed that the SUVmax has the potency as a novel biomarker to predict the survival time of patients with advanced RCC, by multivariate analyses with standard risk factors or risk classifications. FDG accumulation is thought to be indicative of the metabolic activity of a targeted lesion and it has been found to be a useful index in a variety of cancers. It is reasonable that a tumor with high metabolism would show rapid progression and a poor prognosis. It has been reported recently that 18F-FDG PET/CT is useful for evaluating the response to sorafenib and sunitinib treatment of RCC [24, 25]. The results showing that these therapeutics decrease the FDG accumulation of RCC lesions encourage the hypothesis that the FDG accumulation is indicative of the biological activity of RCC. Additionally, it has been reported that intratumoral neutrophils were detected in RCCs showing poor prognosis [26]. SUV may reflect not only the biological activity of cancer cells but also the presence of migrating neutrophils.

To our knowledge, this is the first report to evaluate the impact of SUVmax on survival of patients with advanced RCC. However, the number of patients and the follow-up period were limited. Enrollment for this study continues now, and the impact of SUVmax on the survival of patients with advanced RCC will be more apparent from results from an expanded number of patients and follow-up period.

Conclusions

These preliminary data indicate that the SUVmax evaluated by 18F-FDG-PET/CT has an impact on survival in patients with advanced RCC. Additional study with an expanded number of patients and period of follow-up is necessary.

Conflicts of interests

The authors declare that they have no competing interests.

Declarations

Acknowledgements

This works was supported by Grant for Research and Development Project II (No. 17) of Yokohama City University, Japan and " Establishment of research center for clinical proteomics of post-translational modifications" as part of the Special Coordination Fund for Promoting Science and Technology "Creation and Innovation Centers for Advanced Interdisciplinary ", and Grants-in-Aid for Scientific Research (No. 19591864 and 22591775) from the Ministry of Education, Science, Sports and Culture of Japan.

Authors’ Affiliations

(1)
Department of Urology, Yokohama City University Graduate School of Medicine, 3-9 Fukuura kanazawaku Yokohama, 236-0004, Japan
(2)
Department of Radiology, Yokohama City University Graduate School of Medicine, Yokohama, Japan
(3)
Department of Urology, Kanagawa Cancer Center, Yokohama, Japan
(4)
Department of Urology, Yokosuka Kyosai Hospital, Yokosuka, Japan
(5)
Advanced Medical Research Center, Yokohama City University, Yokohama, Japan

References

  1. Chow WH, Devesa SS, Warren JL, Fraumeni JF: Rising incidence of renal cell carcinoma in the United States. JAMA. 1999, 281: 1628-31. 10.1001/jama.281.17.1628.View ArticlePubMedGoogle Scholar
  2. Linehan WM, Walther MM, Alexander RB, Rosenberg SA: Adoptive immunotherapy of renal cell carcinoma.:studies from the Surgery Branch, National Cancer Institute. Semin Urol. 1993, 11: 41-3.PubMedGoogle Scholar
  3. Janzen NK, Kim HL, Figlin RA, Belldegrun AS: Surveillance after radical or partial nephrectomy for localized renal cell carcinoma and management of recurrent disease. Urol ClinNorth Am. 2003, 30: 843-852. 10.1016/S0094-0143(03)00056-9.View ArticleGoogle Scholar
  4. Motzer RJ, Bander NH, Nanus DM: Renal-cell carcinoma. N Engl J Med. 1996, 335: 865-75. 10.1056/NEJM199609193351207.View ArticlePubMedGoogle Scholar
  5. Naito S, Yamamoto N, Takayama T, Muramoto M, Shinohara N, Nishiyama K, Takahashi A, Maruyama R, Saika T, Hoshi S, Nagao K, Yamamoto S, Sugimura I, Uemura H, Koga S, Takahashi M, Ito F, Ozono S, Terachi T, Naito S, Tomita Y: Prognosis of Japanese Metastatic Renal Cell Carcinoma Patients in the Cytokine Era: A Cooperative Group Report of 1463 Patients. Eur Urol. 2009, 57: 317-26. 10.1016/j.eururo.2008.12.026.View ArticlePubMedGoogle Scholar
  6. McDermott DF, Regan MM, Clark JI, Flaherty LE, Weiss GR, Logan TF, Kirkwood JM, Gordon MS, Sosman JA, Ernstoff MS, Tretter CP, Urba WJ, Smith JW, Margolin KA, Mier JW, Gollob JA, Dutcher JP, Atkins MB: Randomized phase III trial of high-dose interleukin-2 versus subcutaneous interleukin-2 and interferon in patients with metastatic renal cell carcinoma. J Clin Oncol. 2005, 23: 133-141. 10.1200/JCO.2005.03.206. (23)View ArticlePubMedGoogle Scholar
  7. Yang JC, Sherry RM, Steinberg SM, Topalian SL, Schwartzentruber DJ, Hwu P, Seipp CA, Rogers-Freezer L, Morton KE, White DE, Liewehr DJ, Merino MJ, Rosenberg SA: Randomized study of high-dose and low-dose interleukin-2 in patients with metastatic renal cancer. J Clin Oncol. 2003, 21: 3127-3132. 10.1200/JCO.2003.02.122.View ArticlePubMedPubMed CentralGoogle Scholar
  8. Negrier S, Escudier B, Lasset C, Douillard JY, Savary J, Chevreau C, Ravaud A, Mercatello A, Peny J, Mousseau M, Philip T, Tursz T: Recombinant human interleukin-2, recombinant human interferon alfa-2a, or both in metastatic renal cell carcinoma: Groupe Français D'Immunotherapie. N Engl J Med. 1998, 338: 1272-8. 10.1056/NEJM199804303381805.View ArticlePubMedGoogle Scholar
  9. Negrier S, Perol D, Ravaud A, Chevreau C, Bay JO, Delva R, Sevin E, Caty A, Escudier B, For The French Immunotherapy Intergroup: Medroxyprogesterone, interferon alfa-2a, interleukin 2, or combination of both cytokines in patients with metastatic renal carcinoma of intermediate prognosis: Results of a randomized controlled trial. Cancer. 2007, 110: 2468-2477. 10.1002/cncr.23056.View ArticlePubMedGoogle Scholar
  10. Motzer RJ, Hutson TE, Tomczak P, Michaelson MD, Bukowski RM, Rixe O, Oudard S, Negrier S, Szczylik C, Kim ST, Chen I, Bycott PW, Baum CM, Figlin RA: Sunitinib versus interferon alfa in metastatic renal cell carcinoma. N Engl J Med. 2007, 356: 115-124. 10.1056/NEJMoa065044.View ArticlePubMedGoogle Scholar
  11. Escudier B, Eisen T, Stadler WM, Szczylik C, Oudard S, Siebels M, Negrier S, Chevreau C, Solska E, Desai AA, Rolland F, Demkow T, Hutson TE, Gore M, Freeman S, Schwartz B, Shan M, Simantov R, Bukowski RM, TARGET Study Group: Sorafenib in advanced clear cell renal cell carcinoma. N Engl J Med. 2007, 356: 125-134. 10.1056/NEJMoa060655.View ArticlePubMedGoogle Scholar
  12. Hudes G, Carducci M, Tomczak P, Dutcher J, Figlin R, Kapoor A, Staroslawska E, Sosman J, McDermott D, Bodrogi I, Kovacevic Z, Lesovoy V, Schmidt-Wolf IG, Barbarash O, Gokmen E, O'Toole T, Lustgarten S, Moore L, Motzer RJ, Global ARCC Trial: Temsirolimus, interferon alfa, or both for advanced renal-cell carcinoma. N Engl J Med. 2007, 356 (22): 2271-81. 10.1056/NEJMoa066838.View ArticlePubMedGoogle Scholar
  13. Motzer RJ, Escudier B, Oudard S, Hutson TE, Porta C, Bracarda S, Grünwald V, Thompson JA, Figlin RA, Hollaender N, Urbanowitz G, Berg WJ, Kay A, Lebwohl D, Ravaud A, RECORD-1 Study Group: Efficacy of everolimus in advanced renal cell carcinoma: a double-blind, randomised, placebo-controlled phase III trial. Lancet. 2008, 372 (9637): 449-56. 10.1016/S0140-6736(08)61039-9.View ArticlePubMedGoogle Scholar
  14. Motzer RJ, Mazumdar M, Bacik J, Berg W, Amsterdam A, Ferrara J: Survival and prognostic stratification of 670 patients with advanced renal cell carcinoma. J Clin Oncol. 1999, 17: 2530-40.PubMedGoogle Scholar
  15. National Comprehensive Cancer Network: NCCN Clinical Practice Guideline in Oncology: Kidney Cancer V.1. 2011, [http://www.nccn.org/professionals/physician_gls/f_guidelines.asp#site]Google Scholar
  16. Allal AS, Slosman DO, Kebdani T, Allaoua M, Lehmann W, Dulguerov P: Prediction of outcome in head-and-neck cancer oatients using the standardized uptake value of 2-[18F]fluoro-2-deoxy-D-glucose. Int J Radiat Oncol Biol Phys. 2004, 59: 1295-3000. 10.1016/j.ijrobp.2003.12.039.View ArticlePubMedGoogle Scholar
  17. Downey RJ, Akhurst T, Gonen M, Vincent A, Bains MS, Larson S, Rusch V: Preoperative F-18 fluorodeoxyglucose-positron emission tomography maximal standardized uptake value predicts survival after lung cancer resection. J Clin Oncol. 2004, 22: 3255-60. 10.1200/JCO.2004.11.109.View ArticlePubMedGoogle Scholar
  18. Sasaki R, Komaki R, Macapinlac H, Erasmus J, Allen P, Forster K, Putnam JB, Herbst RS, Moran CA, Podoloff DA, Roth JA, Cox JD: [18F] fluorodeoxyglucose uptake by positron emission tomographypredicts outcome of non-small-cell lung cancer. J Clin Oncol. 2005, 23: 1136-43. 10.1200/JCO.2005.06.129.View ArticlePubMedGoogle Scholar
  19. Lee YY, Choi CH, Kim CJ, Kang H, Kim TJ, Lee JW, Lee JH, Bae DS, Kim BG: The prognostic significance of the SUVmax (maximum standardized uptake value for F-18 fluorodeoxyglucose) of the cervical tumor in PET imaging for eary cervical cancer: Preliminary results. Gynecol Oncol. 2009, 115: 65-68. 10.1016/j.ygyno.2009.06.022.View ArticlePubMedGoogle Scholar
  20. Aide N, Cappele O, Bottet P, Bensadoun H, Regeasse A, Comoz F, Sobrio F, Bouvard G, Agostini D: Efficiency of [(18)F]FDG PET in characterising renal cancer and detecting distant metastases: a comparison with CT. Eur J Nucl Med Mol Imaging. 2003, 1236-45. 10.1007/s00259-003-1211-4.Google Scholar
  21. Kang DE, White RL, Zuger JH, Sasser HC, Teigland CM: Clinical use of fluorodeoxyglucose F 18 positron emission tomography for detection of renal cell carcinoma. J Urol. 2004, 171: 1806-9. 10.1097/01.ju.0000120241.50061.e4.View ArticlePubMedGoogle Scholar
  22. Majhail NS, Urbain JL, Albani JM, Kanvinde MH, Rice TW, Novick AC, Mekhail TM, Olencki TE, Elson P, Bukowski RM: F-18 fluorodeoxyglucose positron emission tomography in the evaluation of distant metastases from renal cell carcinoma. J Clin Oncol. 2003, 21: 3995-4000. 10.1200/JCO.2003.04.073.View ArticlePubMedGoogle Scholar
  23. Park JW, Jo MK, Lee HM: Significance of 18F-fluorodeoxyglucose positron-emission tomography/computed tomography for the postoperative surveillance of advanced renal cell carcinoma. BJU Int. 2009, 103: 615-9. 10.1111/j.1464-410X.2008.08150.x.View ArticlePubMedGoogle Scholar
  24. Lyrdal D, Boijsen M, Suurküla M, Lundstam S, Stierner U: Evaluation of sorafenib treatment in metastatic renal cell carcinoma with 2-fluoro-2-deoxyglucose positron emission tomography and computed tomography. Nucl Med Commun. 2009, 30: 519-24. 10.1097/MNM.0b013e32832cc220.View ArticlePubMedGoogle Scholar
  25. Vercellino L, Bousquet G, Baillet G, Barré E, Mathieu O, Just PA, Desgrandchamps F, Misset JL, Hindié E, Moretti JL: 18F-FDG PET/CT imaging for an early assessment of response to sunitinib in metastatic renal carcinoma: preliminary study. Cancer Biother Radiopharm. 2009, 24: 137-44. 10.1089/cbr.2008.0527.View ArticlePubMedGoogle Scholar
  26. Donskov F, von der Maase H: Impact of immune parameters on long-term survival in metastatic renal cell carcinoma. J Clin Oncol. 2006, 24: 1997-2005. 10.1200/JCO.2005.03.9594.View ArticlePubMedGoogle Scholar

    27. Pre-publication history

    1. The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2407/10/667/prepub

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© Namura et al; licensee BioMed Central Ltd. 2010

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 (<url>http://creativecommons.org/licenses/by/2.0</url>), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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