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Dynamic whole-body 18F-FDG PET for differentiating abnormal lesions from physiological uptake

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European Journal of Nuclear Medicine and Molecular Imaging Aims and scope Submit manuscript

Abstract

Purpose

Serial assessment of visual change in 18F-FDG uptake on whole-body 18F-FDG PET imaging was performed to differentiate pathological uptake from physiological uptake in the urinary and gastrointestinal tracts.

Methods

In 88 suspected cancer patients, serial 3-min dynamic whole-body PET imaging was performed four times, from 60 min after 18F-FDG administration. In dynamic image evaluation, high 18F-FDG uptake was evaluated by two nuclear medicine physicians and classified as “changed” or “unchanged” based on change in uptake shape over time. Detectability of pathological uptake based on these criteria was assessed and compared with conventional image evaluation.

Results

Dynamic whole-body PET imaging provided images of adequate quality for visual assessment. Dynamic image evaluation was “changed” in 118/154 regions of high physiological 18F-FDG uptake (77%): in 9/19 areas in the stomach (47%), in 32/39 in the small intestine (82%), in 17/33 in the colon (52%), and in 60/63 in the urinary tract (95%). In the 86 benign or malignant lesions, 84 lesions (98%) were “unchanged.” A high 18F-FDG uptake area that shows no change over time using these criteria is highly likely to represent pathological uptake, with sensitivity of 97%, specificity of 76%, PPV of 70%, NPV of 98%, and accuracy of 84%.

Conclusion

Dynamic whole-body 18F-FDG PET imaging enabled differentiation of pathological uptake from physiological uptake in the urinary and gastrointestinal tracts, based on visual change of uptake shape.

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References

  1. Fletcher JW, Djulbegovic B, Soares HP, Siegel BA, Lowe VJ, Lyman GH, et al. Recommendations on the use of 18F-FDG PET in oncology. J Nucl Med. 2008;49:480–508.

    Article  Google Scholar 

  2. El-Galaly TC, Gormsen LC, Hutchings M. PET/CT for staging: past, present, and future. Semin Nucl Med. 2017;48:4–16.

    Article  Google Scholar 

  3. Shen G, Lan Y, Zhang K, Ren P, Jia Z. Comparison of 18F-FDG PET/CT and DWI for detection of mediastinal nodal metastasis in non-small cell lung cancer: a meta-analysis. PLoS One. 2017;12(3):e0173104. https://doi.org/10.1371/journal.pone.0173104.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  4. Dahlbom M, Reed J, Young J. Implementation of true continuous bed motion in 2-D and 3-D whole-body PET scanning. IEEE Trans Nucl Sci. 2001;48(4):1465–9.

    Article  Google Scholar 

  5. Osborne DR, Acuff S, Cruise S, Syed M, Neveu M, Stuckey A, et al. Quantitative and qualitative comparison of continuous bed motion and traditional step and shoot PET/CT. Am J Nucl Med Mol Imaging. 2014;5(1):56–64.

    PubMed  PubMed Central  Google Scholar 

  6. Karakatsanis NA, Casey ME, Lodge MA, Rahmim A, Zaidi H. Whole-body direct 4D parametric PET imaging employing nested generalized Patlak expectation-maximization reconstruction. Phys Med Biol. 2016;61(15):5456–85.

    Article  Google Scholar 

  7. Braune A, Hofheinz F, Bluth T, Kiss T, Wittenstein J, Scharffenberg M, et al. Comparison of static 18F-FDG-PET/CT (SUV, SUR) and dynamic 18F-FDG-PET/CT (Ki) for quantification of pulmonary inflammation in acute lung injury. J Nucl Med. 2019;60(11):1629–34.

    Article  CAS  Google Scholar 

  8. Rahmim A, Lodge MA, Karakatsanis NA, Panin VY, Zhou Y, McMillan A, et al. Dynamic whole-body PET imaging: principles, potentials and applications. Eur J Nucl Med Mol Imaging. 2019;46:501–18.

    Article  Google Scholar 

  9. Gutman F, Alberini JL, Wartski M, Vilain D, Le Stanc E, Sarandi F, et al. Incidental colonic focal lesions detected by FDG PET/CT. Am J Roentgenol. 2005;185:495–500.

    Article  Google Scholar 

  10. Tatlidil R, Jadvar H, Bading JR, Conti PS. Incidental colonic fluorodeoxyglucose uptake: correlation with colonoscopic and histopathologic findings. Radiology. 2002;224:783–7.

    Article  Google Scholar 

  11. Kostakoglu L, Hardoff R, Mirtcheva R, Goldsmith SJ. PET-CT fusion imaging in differentiating physiologic from pathologic FDG uptake. Radiographics. 2004;24:1411–31.

    Article  Google Scholar 

  12. Drenth JP, Nagengast FM, Oyen WJ. Evaluation of (pre-)malignant colonic abnormalities: endoscopic validation of FDG-PET findings. Eur J Nucl Med. 2001;28:1766–9.

    Article  CAS  Google Scholar 

  13. Kamel EM, Thumshirn M, Truninger K, Schiesser M, Fried M, Padberg B, et al. Significance of incidental 18F-FDG accumulations in the gastrointestinal tract in PET/CT: correlation with endoscopic and histopathologic results. J Nucl Med. 2004;45:1804–10.

    PubMed  Google Scholar 

  14. Israel O, Yefremov N, Bar-Shalom R, Kagana O, Frenkel A, Keidar Z, et al. PET/CT detection of unexpected gastrointestinal foci of 18F-FDG uptake: incidence, localization patterns, and clinical significance. J Nucl Med. 2005;46:758–62.

    PubMed  Google Scholar 

  15. Shinya T, Rai K, Okumura Y, Fujiwara K, Matsuo K, Yonei T, et al. Dual-time-point F-18 FDG PET/CT for evaluation of intrathoracic lymph nodes in patients with non-small cell lung cancer. Clin Nucl Med. 2009;34:216–21.

    Article  Google Scholar 

  16. Matthies A, Hickeson M, Cuchiara A, Alavi A. Dual time point 18F-FDG PET for the evaluation of pulmonary nodules. J Nucl Med. 2002;43:871–5.

    PubMed  Google Scholar 

  17. Nishiyama Y, Yamamoto Y, Monden T, Sasakawa Y, Tsutsui K, Wakabayashi H, et al. Evaluation of delayed additional FDG PET imaging in patients with pancreatic tumour. Nucl Med Commun. 2005;26:895–901.

    Article  Google Scholar 

  18. Lin WY, Tsai SC, Hung GU. Value of delayed 18F-FDG-PET imaging in the detection of hepatocellular carcinoma. Nucl Med Commun. 2005;26:315–21.

    Article  Google Scholar 

  19. Choi EK, Yoo IR, Kim SH, O JH, Choi WH, Na SJ, et al. The clinical value of dual-time point 18F-FDG PET/CT for differentiating extrahepatic cholangiocarcinoma from benign disease. Clin Nucl Med. 2013;38(3):e106–11. https://doi.org/10.1097/RLU.0b013e318266f402.

    Article  PubMed  Google Scholar 

  20. Naganawa S, Yoshikawa T, Yasaka K, Maeda E, Hyashi N, Abe O. Role of delayed-time-point imaging during abdominal and pelvic cancer screening using FDG-PET/CT in the general population. Medicine. 2017;96(46):e8832.

    Article  Google Scholar 

  21. Zade A, Purandare N, Rangarajan V, Shah S, Agarwal A, Kulkarni M, et al. Role of delayed imaging to differentiate intense physiological 18F FDG uptake from peritoneal deposits in patients presenting with intestinal obstruction. Clin Nucl Med. 2012;37(8):783–5. https://doi.org/10.1097/RLU.0b013e31824c5e7d.

    Article  PubMed  Google Scholar 

  22. Toriihara A, Yoshida K, Umehara I, Shibuya H. Normal variants of bowel FDG uptake in dual-time-point PET/CT imaging. Ann Nucl Med. 2011;25(3):173–8. https://doi.org/10.1007/s12149-010-0439-x.

    Article  PubMed  Google Scholar 

  23. Miyake KK, Nakamoto J, Torashi K. Dual-time-point 18F-FDG PET/CT in patients with colorectal cancer: clinical value of early delayed scanning. Ann Nucl Med. 2012;26:492–500.

    Article  CAS  Google Scholar 

  24. Uemura Y, Demura Y, Morikawa M, Anzai M, Kadowaki M, Ameshima S, et al. Prognostic value of dual-time-point 18F-FDG PET for idiopathic pulmonary fibrosis. J Nucl Med. 2015;56:1869–75.

    Article  Google Scholar 

  25. Yoon HJ, Yoo J, Lee DH, Kim BS. Enhanced application of 18F-FDG PET/CT in bladder cancer by adding early dynamic acquisition to a standard delayed PET protocol. Clin Nucl Med. 2017;42(10):749–55.

    Article  Google Scholar 

  26. Humbert O, Lasserre M, Bertaut A, Fumoleau P, Coutant C, Brunotte F, et al. Breast cancer blood flow and metabolism on dual-acquisition 18F-FDG PET: correlation with tumor phenotype and neoadjuvant chemotherapy response. J Nucl Med. 2018;59:1035–41.

    Article  CAS  Google Scholar 

  27. van Sluis J, Boellaard R, Somasundaram A, van Snick P, Borra R, Dierckx R, et al. Image quality and semi-quantitative measurements of the Siemens Biograph Vision PET/CT: initial experiences and comparison with Siemens Biograph mCT PET/CT. J Nucl Med. 2019. https://doi.org/10.2967/jnumed.119.227801.

  28. Nishimura M, Tamaki N, Matsushima S, Yamada S, Nii T, Domoto H, et al. Uptake changes on the whole-body dynamic 18F-FDG PET may assess tissue characterization. Comparison with the conventional delayed scan. J Nucl Med. 2019;60:1284.

    Article  Google Scholar 

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Acknowledgments

The authors wish to thank Takeshi Nii, Hiroshi Domoto, Yasutomo Tanada, Koki Shirako, and Azusa Tahata (Department of Radiological Technology, University Hospital, Kyoto Prefectural University of Medicine, Kyoto, Japan) for their technical support.

Funding

This study was funded by a grant from MEXT KAKENHI (number JP182004140).

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Corresponding author

Correspondence to Nagara Tamaki.

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Conflict of interest

Kei Yamada has received research grants from Doctor-NET Inc., Fukushima SIC Applied Engineering Inc., Nihon Mediphysics Co., Ltd., Fuji Pharma Co., Ltd., and Daiichi-Sankyo Co., Ltd. All other authors declare that they have no conflict of interest.

Ethical approval

All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional and national research committee and with the 1964 Helsinki Declaration and its later amendments or comparable ethical standards. No animals were used in the present study, by any author.

Informed consent

Based on the Ethical Guidelines for Medical and Health Research Involving Human Subjects of the Ministry of Health, Labour and Welfare, a waiver of informed consent for the retrospective analyses of the anonymized clinical data in this study was obtained from the Institutional Review Board of Kyoto Prefectural University of Medicine, Japan.

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This article is part of the Topical Collection on Oncology – General

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Nishimura, M., Tamaki, N., Matsushima, S. et al. Dynamic whole-body 18F-FDG PET for differentiating abnormal lesions from physiological uptake. Eur J Nucl Med Mol Imaging 47, 2293–2300 (2020). https://doi.org/10.1007/s00259-020-04726-w

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  • DOI: https://doi.org/10.1007/s00259-020-04726-w

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