Results of a Prospective Trial to Compare 68Ga-DOTA-TATE with SiPM-Based PET/CT vs. Conventional PET/CT in Patients with Neuroendocrine Tumors

Lucia Baratto, Akira Toriihara, Negin Hatami, Carina M Aparici, Guido Davidzon, Craig S Levin, Andrei Iagaru, Lucia Baratto, Akira Toriihara, Negin Hatami, Carina M Aparici, Guido Davidzon, Craig S Levin, Andrei Iagaru

Abstract

We prospectively enrolled patients with neuroendocrine tumors (NETs). They underwent a single 68Ga-DOTA-TATE injection followed by dual imaging and were randomly scanned using first either the conventional or the silicon photomultiplier (SiPM) positron emission tomography/computed tomography (PET/CT), followed by imaging using the other system. A total of 94 patients, 44 men and 50 women, between 35 and 91 years old (mean ± SD: 63 ± 11.2), were enrolled. Fifty-two out of ninety-four participants underwent SiPM PET/CT first and a total of 162 lesions were detected using both scanners. Forty-two out of ninety-four participants underwent conventional PET/CT first and a total of 108 lesions were detected using both scanners. Regardless of whether SiPM-based PET/CT was used first or second, maximum standardized uptake value (SUVmax) of lesions measured on SiPM was on average 20% higher when comparing two scanners with all enrolled patients, and the difference was statistically significant. SiPM-based PET/CT detected 19 more lesions in 13 patients compared with conventional PET/CT. No lesions were only identified by conventional PET/CT. In conclusion, we observed higher SUVmax for lesions measured from SiPM PET/CT compared with conventional PET/CT regardless of the order of the scans. SiPM PET/CT allowed for identification of more lesions than conventional PET/CT. While delayed imaging can lead to higher SUVmax in cancer lesions, in the series of lesions identified when SiPM PET/CT was used first, this was not the case; therefore, the data suggest superior performance of the SiPM PET/CT scanner in visualizing and quantifying lesions.

Keywords: 68Ga-DOTA-TATE PET; PET/CT; neuroendocrine tumor; silicon photomultiplier.

Conflict of interest statement

The authors declare no conflict of interest.

Figures

Figure 1
Figure 1
Flowchart of the study population.
Figure 2
Figure 2
A 65-year-old woman with metastatic NET of unknown primary, referred for subsequent treatment strategy after chemotherapy. SiPM-based PET/CT was performed first at 72 min after injection of 4.2 mCi of 68Ga-DOTA-TATE. Conventional PET/CT was performed second at 96 min after injection. Red arrows mark an additional lesion seen in the dome of the liver only on SiPM-based PET/CT (A,B1), not on conventional PET/CT (B3,B4,E). Blue arrows mark bone lesions seen on conventional PET/CT (C3,C4,D3,D4,E) but more conspicuous on SiPM-based PET/CT (A,C1,C2,D1,D2).
Figure 3
Figure 3
A 59-year-old man with metastatic small bowel NET, referred for subsequent treatment strategy after small bowel resection. Conventional PET/CT was performed first at 85 min after injection of 4.5 mCi of 68Ga-DOTA-TATE. SiPM-based PET/CT was performed second at 110 min after injection. Red arrows mark an additional lesion seen in the right lobe of the liver only on SiPM-based PET/CT (B3,B4,E) not on conventional PET/CT (A,B1,B2). Blue arrows mark liver lesions seen on conventional PET/CT (A,C1,C2,D1,D2) but more conspicuous on SiPM-based PET/CT (C3,C4,D3,D4,E).

References

    1. Boellaard R., Delgado-Bolton R., Oyen W.J., Giammarile F., Tatsch K., Eschner W., Verzijlbergen F.J., Barrington S.F., Pike L.C., Weber W.A., et al. FDG PET/CT: EANM procedure guidelines for tumour imaging: Version 2.0. Eur. J. Nucl. Med. Mol. Imaging. 2015;42:328–354. doi: 10.1007/s00259-014-2961-x.
    1. Jadvar H., Colletti P.M., Delgado-Bolton R., Esposito G., Krause B.J., Iagaru A.H., Nadel H., Quinn D.I., Rohren E., Subramaniam R.M., et al. Appropriate Use Criteria for (18)F-FDG PET/CT in Restaging and Treatment Response Assessment of Malignant Disease. J. Nucl. Med. 2017;58:2026–2037. doi: 10.2967/jnumed.117.197988.
    1. Hope T.A., Bergsland E.K., Bozkurt M.F., Graham M., Heaney A.P., Herrmann K., Howe J.R., Kulke M.H., Kunz P.L., Mailman J., et al. Appropriate Use Criteria for Somatostatin Receptor PET Imaging in Neuroendocrine Tumors. J. Nucl. Med. 2018;59:66–74. doi: 10.2967/jnumed.117.202275.
    1. Virgolini I., Ambrosini V., Bomanji J.B., Baum R.P., Fanti S., Gabriel M., Papathanasiou N.D., Pepe G., Oyen W., De Cristoforo C., et al. Procedure guidelines for PET/CT tumour imaging with 68Ga-DOTA-conjugated peptides: 68Ga-DOTA-TOC, 68Ga-DOTA-NOC, 68Ga-DOTA-TATE. Eur. J. Nucl. Med. Mol. Imaging. 2010;37:2004–2010. doi: 10.1007/s00259-010-1512-3.
    1. Spanoudaki V., Levin C.S. Photo-detectors for time of flight positron emission tomography (ToF-PET) Sensors. 2010;10:10484–10505. doi: 10.3390/s101110484.
    1. Van der Vos C.S., Koopman D., Rijnsdorp S., Arends A.J., Boellaard R., van Dalen J.A., Lubberink M., Willemsen A.T.M., Visser E.P. Quantification, improvement, and harmonization of small lesion detection with state-of-the-art PET. Eur. J. Nucl. Med. Mol. Imaging. 2017;44:4–16. doi: 10.1007/s00259-017-3727-z.
    1. Levin C.S., Maramraju S.H., Khalighi M.M., Deller T.W., Delso G., Jansen F. Design Features and Mutual Compatibility Studies of the Time-of-Flight PET Capable GE SIGNA PET/MR System. IEEE Trans. Med. Imaging. 2016;35:1907–1914. doi: 10.1109/TMI.2016.2537811.
    1. Hsu D.F.C., Ilan E., Peterson W.T., Uribe J., Lubberink M., Levin C.S. Studies of a Next-Generation Silicon-Photomultiplier-Based Time-of-Flight PET/CT System. J. Nucl. Med. 2017;58:1511–1518. doi: 10.2967/jnumed.117.189514.
    1. Baratto L., Park S.Y., Hatami N., Davidzon G., Srinivas S., Gambhir S.S., Iagaru A. 18F-FDG silicon photomultiplier PET/CT: A pilot study comparing semi-quantitative measurements with standard PET/CT. PLoS ONE. 2017;12:e0178936. doi: 10.1371/journal.pone.0178936.
    1. Lantos J., Mittra E.S., Levin C.S., Iagaru A. Standard OSEM vs. regularized PET image reconstruction: Qualitative and quantitative comparison using phantom data and various clinical radiopharmaceuticals. Am. J. Nucl. Med. Mol. Imaging. 2018;8:110–118.
    1. Kitajima K., Suzuki K., Nakamoto Y., Onishi Y., Sakamoto S., Senda M., Kita M., Sugimura K. Low-dose non-enhanced CT versus full-dose contrast-enhanced CT in integrated PET/CT studies for the diagnosis of uterine cancer recurrence. Eur. J. Nucl. Med. Mol. Imaging. 2010;37:1490–1498. doi: 10.1007/s00259-010-1440-2.
    1. Fuentes-Ocampo F., Lopez-Mora D.A., Flotats A., Paillahueque G., Camacho V., Duch J., Fernandez A., Domenech A., Estorch M., Carrio I. Digital vs. analog PET/CT: Intra-subject comparison of the SUVmax in target lesions and reference regions. Eur. J. Nucl. Med. Mol. Imaging. 2019;46:1745–1750. doi: 10.1007/s00259-018-4256-0.
    1. Lopez-Mora D.A., Flotats A., Fuentes-Ocampo F., Camacho V., Fernandez A., Ruiz A., Duch J., Sizova M., Domenech A., Estorch M., et al. Comparison of image quality and lesion detection between digital and analog PET/CT. Eur. J. Nucl. Med. Mol. Imaging. 2019;46:1383–1390. doi: 10.1007/s00259-019-4260-z.
    1. Torabi M., Aquino S.L., Harisinghani M.G. Current concepts in lymph node imaging. J. Nucl. Med. 2004;45:1509–1518.
    1. Baratto L., Duan H., Ferri V., Khalighi M., Iagaru A. The Effect of Various beta Values on Image Quality and Semiquantitative Measurements in 68Ga-RM2 and 68Ga-PSMA-11 PET/MRI Images Reconstructed with a Block Sequential Regularized Expectation Maximization Algorithm. Clin. Nucl. Med. 2020;45:506–513. doi: 10.1097/RLU.0000000000003075.

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