Optimal scan time for evaluation of parathyroid adenoma with [(18)F]-fluorocholine PET/CT

Sebastijan Rep, Luka Lezaic, Tomaz Kocjan, Marija Pfeifer, Mojca Jensterle Sever, Urban Simoncic, Petra Tomse, Marko Hocevar, Sebastijan Rep, Luka Lezaic, Tomaz Kocjan, Marija Pfeifer, Mojca Jensterle Sever, Urban Simoncic, Petra Tomse, Marko Hocevar

Abstract

Background: Parathyroid adenomas, the most common cause of primary hyperparathyroidism, are benign tumours which autonomously produce and secrete parathyroid hormone. [(18)F]-fluorocholine (FCH), PET marker of cellular proliferation, was recently demonstrated to accumulate in lesions representing enlarged parathyroid tissue; however, the optimal time to perform FCH PET/CT after FCH administration is not known. The aim of this study was to determine the optimal scan time of FCH PET/CT in patients with primary hyperparathyroidism.

Patients and methods: 43 patients with primary hyperparathyroidism were enrolled in this study. A triple-phase PET/CT imaging was performed five minutes, one and two hours after the administration of FCH. Regions of interest (ROI) were placed in lesions representing enlarged parathyroid tissue and thyroid tissue. Standardized uptake value (SUVmean), retention index and lesion contrast for parathyroid and thyroid tissue were calculated.

Results: Accumulation of FCH was higher in lesions representing enlarged parathyroid tissue in comparison to the thyroid tissue with significantly higher SUVmean in the second and in the third phase (p < 0.0001). Average retention index decreased significantly between the first and the second phase and increased significantly between the second and the third phase in lesions representing enlarged parathyroid tissue and decreased significantly over all three phases in thyroid tissue (p< 0.0001). The lesion contrast of lesions representing enlarged parathyroid tissue and thyroid tissue was significantly better in the second and the third phase compared to the first phase (p < 0.05).

Conclusions: According to the results the optimal scan time of FCH PET/CT for localization of lesions representing enlarged parathyroid tissue is one hour after administration of the FCH.

Keywords: [18F]-fluorocholine PET/CT; lesion contrast; lesions representing enlarged parathyroid tissue; retention index; standardized up-take value; triple-phase.

Figures

FIGURE 1.
FIGURE 1.
Different SUVmean in all three phases of the described kinetics of FCH in LREPT and thyroid tissue.
FIGURE 2.
FIGURE 2.
Retention index (RI) between the second and the third phase (RI23) versus RI between the first and the second phase (RI12) for all LREPT (A), and for thyroid tissue (B). Positive (negative) values of both RI12 and RI23 represent SUVmean increase (decrease) through different phases; whereas positive (negative) RI12 and negative (positive) RI23 represent an increase (decrease) of SUVmean after the first phase, followed by a decrease (increase) after the second phase.
FIGURE 3.
FIGURE 3.
(A) The number of lesions in ranges of lesion contrast (LC) values for all three phases; for both positive and negative LC. (B) The number of both positive and negative lesions having absolute LC value equal or greater to the value on horizontal axis.
FIGURE 4.
FIGURE 4.
A secluded lower left LREPT. FCH PET/CT was performed in triple-phase after administration of 100 MBq of FCH. The LREPT is well delineated according to the thyroid tissue on PET axial image in the first (A1), the second (A2) and the third phase (A3). SUVmean in the LREPT and the thyroid tissue was in the first phase 6.3 and 3.6, in the second phase 7.1 and 3, and in the third phase 6.6 and 2.9. The CT axial image of the LREPT and the thyroid tissue in all three phases (B1, B2, B3), and the FCH PET/CT axial fusion image in all three phases (C1, C2, C3).

References

    1. Lew JI, Solorzano CC. Surgical management of primary hyperparathyroidism: state of the art. Surg Clin North Am. 2009;89:1205–25.
    1. Wada Y, Kunimura T, Sato S, Hisayuki T, Sato M, Imataka H, et al. Proliferating potential and apoptosis in the development of secondary hyperparathyroidism: a study based on Ki-67 immunohistochemical staining and the terminal dUTP nick-end labeling assay. Ther Apher Dial. 2008;12:319–28.
    1. Yamaguchi S, Yachiku S, Morikawa M. Analysis of proliferative activity of the parathyroid glands using proliferating cell nuclear antigen in patients with hyperparathyroidism. J Clin Endocrinol Metab. 1997;82:2681–8.
    1. Allendorf J, DiGorgi M, Spanknebel K, Inabnet W, Chabot J, Logerfo P. 1112 consecutive bilateral neck explorations for primary hyperparathyroidism. World J Surg. 2007;31:2075–80.
    1. Dowthwaite SA, Young JE, Pasternak JD, Yoo J. Surgical management of primary hyperparathyroidism. J Clin Densitom. 2013;16:48–53.
    1. Wang CA. Surgical management of primary hyperparathyroidism. Curr Probl Surg. 1985;22:1–50.
    1. Ruda JM, Hollenbeak CS, Stack BC., Jr A systematic review of the diagnosis and treatment of primary hyperparathyroidism from 1995 to 2003. Otolaryngol Head Neck Surg. 2005;132:359–72.
    1. Miccoli P, Pinchera A, Cecchini G, Conte M, Bendinelli C, Vignali E, et al. Minimally invasive, video-assisted parathyroid surgery for primary hyperparathyroidism. J Endocrinol Invest. 1997;20:429–30.
    1. Goldstein RE, Blevins L, Delbeke D, Martin WH. Effect of minimally invasive radioguided parathyroidectomy on efficacy, length of stay, and costs in the management of primary hyperparathyroidism. Ann Surg. 2000;231:732–42.
    1. Sosa JA, Udelsman R. Minimally invasive parathyroidectomy. Surg Oncol. 2003;12:125–34.
    1. Grant CS, Thompson G, Farley D, van Heerden J. Primary hyperparathyroidism surgical management since the introduction of minimally invasive parathyroidectomy: Mayo Clinic experience. Arch Surg. 2005;140:472–479.
    1. Coakley AJ, Kettle AG, Wells CP, O’Doherty MJ, Collins RE. 99mTc sestamibi--a new agent for parathyroid imaging. Nucl Med Commun. 1989;10:791–4.
    1. Borley NR, Collins RE, O’Doherty M, Coakley A. Technetium-99m sestamibi parathyroid localization is accurate enough for scan-directed unilateral neck exploration. Br J Surg. 1996;83:989–91.
    1. Carneiro-Pla DM, Solorzano CC, Irvin GL., 3rd Consequences of targeted parathyroidectomy guided by localization studies without intraoperative parathyroid hormone monitoring. J Am Coll Surg. 2006;202:715–22.
    1. Lavely WC, Goetze S, Friedman KP, Leal JP, Zhang Z, Garret-Mayer E, et al. Comparison of SPECT/CT, SPECT, and planar imaging with single- and dual-phase (99m)Tc-sestamibi parathyroid scintigraphy. J Nucl Med. 2007;48:1084–9.
    1. Berri RN, Lloyd LR. Detection of parathyroid adenoma in patients with primary hyperparathyroidism: the use of office-based ultrasound in preoperative localization. Am J Surg. 2006;191:311–4.
    1. Haber RS, Kim CK, Inabnet WB. Ultrasonography for preoperative localization of enlarged parathyroid glands in primary hyperparathyroidism: comparison with (99m)technetium sestamibi scintigraphy. Clin Endocrinol (Oxf) 2002;57:241–9.
    1. Mapelli P, Busnardo E, Magnani P, Freschi M, Picchio M, Gianolli L, et al. Incidental finding of parathyroid adenoma with 11C-choline PET/CT. Clin Nucl Med. 2012;37:593–5.
    1. Quak E, Lheureux S, Reznik Y, Bardet S, Aide N. F18-choline, a novel PET tracer for parathyroid adenoma? J Clin Endocrinol Metab. 2013;98:3111–2.
    1. Lezaic L, Rep S, Jensterle SM, Hocevar M, Fettich J. 18F-fluorocholine PET/CT for localization of hyper functioning parathyroid tissue in primary hyper-parathyroidism: a pilot study. Eur J Nucl Med Mol Imaging. 2014;41:2083–9.
    1. Nakayama M, Okizaki A, Ishitoya S, Sakaguchi M, Sato J, Aburano T. Dual-time-point F-18 FDG PET/CT imaging for differentiating the lymph nodes between malignant lymphoma and benign lesions. Ann Nucl Med. 2013;27:163–9.
    1. Cherry SR, Sorenson JA, Phelps ME. Physics in nuclear medicine. 4th edition. Philadelphia: Elsevier/Saunders; 2012. pp. 253–270.
    1. Chien D, Jacene H. Imaging of parathyroid glands. Otolaryngol Clin North Am. 2010;43:399–415.
    1. Hellman P, Ahlström H, Bergström M, Sundin A, Långström B, Westerberg G, et al. Positron emission tomography with 11C-methionine in hyperparathyroidism. Surgery. 1994;116:974–81.
    1. Otto D, Boerner AR, Hofmann M, Brunkhorst T, Meyer GJ, Petrich T, et al. Pre-operative localisation of hyperfunctional parathyroid tissue with 11C-methionine PET. Eur J Nucl Med Mol Imaging. 2004;31:1405–12.
    1. Oksüz MO, Dittmann H, Wicke C, Müssig K, Bares R, Pfannenberg C, et al. Accuracy of parathyroid imaging: a comparison of planar scintigraphy, SPECT, SPECT/CT, and C-11 methionine PET for the detection of parathyroid adenomas and glandular hyperplasia. Diagn Interv Radiol. 2011;17:297–307.
    1. Giussani A, Janzen T, Uusijarvi-Lizana H, Tavola F, Zankl M, Sydoff M, et al. A compartmental model for biokinetics and dosimetry of 18F-choline in prostate cancer patients. J Nucl Med. 2012;53:985–93.
    1. Tavola F, Janzen T, Giussani A, Facchinetti D, Veronese I, Uusijärvi-Lizana H, et al. Nonlinear compartmental model of 18F-choline. Nucl Med Biol. 2012;39:261–8.
    1. DeGrado TR, Coleman RE, Wang S, Baldwin SW, Orr MD, Robertson CN, et al. Synthesis and evaluation of 18F-labeled choline as an oncologic tracer for positron emission tomography: initial findings in prostate cancer. Cancer Res. 2001;61:110–7.

Source: PubMed

3
订阅