메뉴 건너뛰기




Volumn 55, Issue 9, 2014, Pages 1499-1505

Preclinical evaluation of a high-affinity 18F-trifluoroborate octreotate derivative for somatostatin receptor imaging

Author keywords

1 step 18F labeling; 18F BF3; Octreotate; Octreotide; Positron emission tomography; Somatostatin receptor

Indexed keywords

FLUORINE; FLUORINE 18; N PROPARGYL N,N DIMETHYL AMMONIOMETHYLTRIFLUOROBORATE F 18; RADIOPHARMACEUTICAL AGENT; SOMATOSTATIN RECEPTOR; TRIFLUOROBORATE OCTREOTATE F 18 DERIVATIVE; UNCLASSIFIED DRUG; DIAGNOSTIC AGENT; DRUG DERIVATIVE; OCTREOTIDE;

EID: 84907010619     PISSN: 01615505     EISSN: 2159662X     Source Type: Journal    
DOI: 10.2967/jnumed.114.137836     Document Type: Article
Times cited : (80)

References (37)
  • 1
    • 74849111472 scopus 로고    scopus 로고
    • Peptide receptor radionuclide therapy in patients with gastroenteropancreatic neuroendocrine tumors
    • Kwekkeboom DJ, de Herder WW, van Eijck CH, et al. Peptide receptor radionuclide therapy in patients with gastroenteropancreatic neuroendocrine tumors. Semin Nucl Med. 2010;40:78-88.
    • (2010) Semin Nucl Med , vol.40 , pp. 78-88
    • Kwekkeboom, D.J.1    De Herder, W.W.2    Van Eijck, C.H.3
  • 2
    • 0034892549 scopus 로고    scopus 로고
    • Somatostatin receptormediated imaging and therapy: Basic science, current knowledge, limitations and future perspectives
    • Breeman WAP, de Jong M, Kwekkeboom DJ, et al. Somatostatin receptormediated imaging and therapy: basic science, current knowledge, limitations and future perspectives. Eur J Nucl Med. 2001;28:1421-1429.
    • (2001) Eur J Nucl Med , vol.28 , pp. 1421-1429
    • Breeman, W.A.P.1    De Jong, M.2    Kwekkeboom, D.J.3
  • 3
    • 33749674563 scopus 로고    scopus 로고
    • Design synthesis, and biological evaluation of somatostatin-based radiopeptides
    • Ginj M, Schmitt JS, Chen JH, et al. Design, synthesis, and biological evaluation of somatostatin-based radiopeptides. Chem Biol. 2006;13:1081-1090.
    • (2006) Chem Biol , vol.13 , pp. 1081-1090
    • Ginj, M.1    Schmitt, J.S.2    Chen, J.H.3
  • 4
    • 33846435309 scopus 로고    scopus 로고
    • Influence of different spacers on the biological profile of a DOTA-somatostatin analogue
    • Antunes P, Ginj M, Walter MA, et al. Influence of different spacers on the biological profile of a DOTA-somatostatin analogue. Bioconjug Chem. 2007;18: 84-92.
    • (2007) Bioconjug Chem , vol.18 , pp. 84-92
    • Antunes, P.1    Ginj, M.2    Walter, M.A.3
  • 5
    • 77449132297 scopus 로고    scopus 로고
    • Somatostatin receptor-based imaging and therapy of gastroenteropancreatic neuroendocrine tumors
    • Kwekkeboom DJ, Kam BL, van Essen M, et al. Somatostatin receptor-based imaging and therapy of gastroenteropancreatic neuroendocrine tumors. Endocr Relat Cancer. 2010;17:R53-R73.
    • (2010) Endocr Relat Cancer , vol.17 , pp. R53-R73
    • Kwekkeboom, D.J.1    Kam, B.L.2    Van Essen, M.3
  • 6
    • 10744229252 scopus 로고    scopus 로고
    • SPECT/CT hybrid imaging with In-111- pentetreotide in assessment of neuroendocrine tumours
    • Krausz Y, Keidar Z, Kogan I, et al. SPECT/CT hybrid imaging with In-111- pentetreotide in assessment of neuroendocrine tumours. Clin Endocrinol (Oxf). 2003;59:565-573.
    • (2003) Clin Endocrinol (Oxf) , vol.59 , pp. 565-573
    • Krausz, Y.1    Keidar, Z.2    Kogan, I.3
  • 7
    • 34748835270 scopus 로고    scopus 로고
    • Comparison of Ga-68-DOTATOC PET and In-111-DTPAOC (Octreoscan) SPECT in patients with neuroendocrine tumours
    • Buchmann I, Henze M, Engelbrecht S, et al. Comparison of Ga-68-DOTATOC PET and In-111-DTPAOC (Octreoscan) SPECT in patients with neuroendocrine tumours. Eur J Nucl Med Mol Imaging. 2007;34:1617-1626.
    • (2007) Eur J Nucl Med Mol Imaging , vol.34 , pp. 1617-1626
    • Buchmann, I.1    Henze, M.2    Engelbrecht, S.3
  • 8
    • 27744479810 scopus 로고    scopus 로고
    • 111In-DTPA0]octreotide: Does tumor or pancreas uptake correlate with the rate of internalization?
    • Storch D, Behe M, Walter MA, et al. Evaluation of [99mTc/EDDA/HYNIC0] octreotide derivatives compared with [111In-DOTA0,Tyr3, Thr8]octreotide and [111In-DTPA0]octreotide: does tumor or pancreas uptake correlate with the rate of internalization? J Nucl Med. 2005;46:1561-1569.
    • (2005) J Nucl Med , vol.46 , pp. 1561-1569
    • Storch, D.1    Behe, M.2    Walter, M.A.3
  • 9
    • 2642657309 scopus 로고    scopus 로고
    • 99mTc-P829
    • Virgolini I, Leimer M, Handmaker H, et al. Somatostatin receptor subtype specificity and in vivo binding of a novel tumor tracer, 99mTc-P829. Cancer Res. 1998;58:1850-1859.
    • (1998) Cancer Res , vol.58 , pp. 1850-1859
    • Virgolini, I.1    Leimer, M.2    Handmaker, H.3
  • 10
    • 0038282731 scopus 로고    scopus 로고
    • 111In-DTPA-octreotide for diagnosis of somatostatin receptor-expressing tumors
    • Gabriel M, Decristoforo C, Donnemiller E, et al. An intrapatient comparison of 99mTc-EDDA/HYNIC-TOC with 111In-DTPA-octreotide for diagnosis of somatostatin receptor-expressing tumors. J Nucl Med. 2003;44:708-716.
    • (2003) J Nucl Med , vol.44 , pp. 708-716
    • Gabriel, M.1    Decristoforo, C.2    Donnemiller, E.3
  • 11
    • 11144228601 scopus 로고    scopus 로고
    • 3-octreotate using a cross-bridged macrocyclic chelator
    • Sprague JE, Peng YJ, Sun XK, et al. Preparation and biological evaluation of copper-64-labeled tyr3-octreotate using a cross-bridged macrocyclic chelator. Clin Cancer Res. 2004;10:8674-8682.
    • (2004) Clin Cancer Res , vol.10 , pp. 8674-8682
    • Sprague, J.E.1    Peng, Y.J.2    Sun, X.K.3
  • 12
    • 34248529824 scopus 로고    scopus 로고
    • 3-octreotide PET in neuroendocrine tumors: Comparison with somatostatin receptor scintigraphy and CT
    • Gabriel M, Decristoforo C, Kendler D, et al. Ga-68-DOTA-Tyr3-octreotide PET in neuroendocrine tumors: comparison with somatostatin receptor scintigraphy and CT. J Nucl Med. 2007;48:508-518.
    • (2007) J Nucl Med , vol.48 , pp. 508-518
    • Gabriel, M.1    Decristoforo, C.2    Kendler, D.3
  • 13
    • 84863919413 scopus 로고    scopus 로고
    • 3-octreotate using a phosphonic acid-based cross-bridged macrocyclic chelator
    • Guo Y, Ferdani R, Anderson CJ. Preparation and biological evaluation of Cu-64 labeled tyr3-octreotate using a phosphonic acid-based cross-bridged macrocyclic chelator. Bioconjug Chem. 2012;23:1470-1477.
    • (2012) Bioconjug Chem , vol.23 , pp. 1470-1477
    • Guo, Y.1    Ferdani, R.2    Anderson, C.J.3
  • 14
    • 0037870080 scopus 로고    scopus 로고
    • PET imaging of somatostatin receptors: Design, synthesis and preclinical evaluation of a novel F-18-labelled, carbohydrated analogue of octreotide
    • Wester HJ, Schottelius M, Scheidhauer K, et al. PET imaging of somatostatin receptors: design, synthesis and preclinical evaluation of a novel F-18-labelled, carbohydrated analogue of octreotide. Eur J Nucl Med Mol Imaging. 2003;30: 117-122.
    • (2003) Eur J Nucl Med Mol Imaging , vol.30 , pp. 117-122
    • Wester, H.J.1    Schottelius, M.2    Scheidhauer, K.3
  • 15
    • 2642527947 scopus 로고    scopus 로고
    • 18F-labeled RGD and octreotide analogs
    • Poethko T, Schottelius M, Thumshim G, et al. Two-step methodology for highyield routine radiohalogenation of peptides: 18F-labeled RGD and octreotide analogs. J Nucl Med. 2004;45:892-902.
    • (2004) J Nucl Med , vol.45 , pp. 892-902
    • Poethko, T.1    Schottelius, M.2    Thumshim, G.3
  • 16
    • 80052615497 scopus 로고    scopus 로고
    • Targeting somatostatin receptors: Preclinical evaluation of novel F-18-fluoroethyltriazole-tyr3-octreotate analogs for PET
    • Leyton J, Iddon L, Perumal M, et al. Targeting somatostatin receptors: preclinical evaluation of novel F-18-fluoroethyltriazole-tyr3-octreotate analogs for PET. J Nucl Med. 2011;52:1441-1448.
    • (2011) J Nucl Med , vol.52 , pp. 1441-1448
    • Leyton, J.1    Iddon, L.2    Perumal, M.3
  • 17
    • 0034949018 scopus 로고    scopus 로고
    • 3-octreotide: First results in patients with meningiomas
    • Henze M, Schuhmacher J, Hipp P, et al. PET imaging of somatostatin receptors using [68GA]DOTA-D-Phe1-Tyr3-octreotide: first results in patients with meningiomas. J Nucl Med. 2001;42:1053-1056.
    • (2001) J Nucl Med , vol.42 , pp. 1053-1056
    • Henze, M.1    Schuhmacher, J.2    Hipp, P.3
  • 18
    • 73349102167 scopus 로고    scopus 로고
    • A comparison of Ga-68-DOTATATE and F-18-FDG PET/CT in pulmonary neuroendocrine tumors
    • Kayani I, Conry BG, Groves AM, et al. A comparison of Ga-68-DOTATATE and F-18-FDG PET/CT in pulmonary neuroendocrine tumors. J Nucl Med. 2009;50: 1927-1932.
    • (2009) J Nucl Med , vol.50 , pp. 1927-1932
    • Kayani, I.1    Conry, B.G.2    Groves, A.M.3
  • 19
    • 83755171298 scopus 로고    scopus 로고
    • Ga-68-DOTATOC versus Ga-68- DOTATATE PET/CT in functional imaging of neuroendocrine tumors
    • Poeppel TD, Binse I, Petersenn S, et al. Ga-68-DOTATOC versus Ga-68- DOTATATE PET/CT in functional imaging of neuroendocrine tumors. J Nucl Med. 2011;52:1864-1870.
    • (2011) J Nucl Med , vol.52 , pp. 1864-1870
    • Poeppel, T.D.1    Binse, I.2    Petersenn, S.3
  • 20
  • 21
    • 44249097810 scopus 로고    scopus 로고
    • Image quality with non-standard nuclides in PET
    • Laforest R, Liu X. Image quality with non-standard nuclides in PET. Q J Nucl Med Mol Imaging. 2008;52:151-158.
    • (2008) Q J Nucl Med Mol Imaging , vol.52 , pp. 151-158
    • Laforest, R.1    Liu, X.2
  • 22
    • 79953675989 scopus 로고    scopus 로고
    • Effect of the positron range of F-18, Ga-68 and I-124 on PET/CT in lung-equivalent materials
    • Kemerink GJ, Visser MGW, Franssen R, et al. Effect of the positron range of F-18, Ga-68 and I-124 on PET/CT in lung-equivalent materials. Eur J Nucl Med Mol Imaging. 2011;38:940-948.
    • (2011) Eur J Nucl Med Mol Imaging , vol.38 , pp. 940-948
    • Kemerink, G.J.1    Visser, M.G.W.2    Franssen, R.3
  • 23
    • 1642397183 scopus 로고    scopus 로고
    • Hydration of the fluoride anion: Structures and absolute hydration free energy from first-principles electronic structure calculations
    • Zhan C-G, Dixon DA. Hydration of the fluoride anion: structures and absolute hydration free energy from first-principles electronic structure calculations. J Phys Chem A. 2004;108:2020-2029.
    • (2004) J Phys Chem A , vol.108 , pp. 2020-2029
    • Zhan, C.-G.1    Dixon, D.A.2
  • 24
    • 84861481740 scopus 로고    scopus 로고
    • First experience with clinical-grade F-18 FPP (RGD)(2): An automated multi-step radiosynthesis for clinical PET studies
    • Chin FT, Shen B, Liu SL, et al. First experience with clinical-grade F-18 FPP (RGD)(2): an automated multi-step radiosynthesis for clinical PET studies. Mol Imaging Biol. 2012;14:88-95.
    • (2012) Mol Imaging Biol , vol.14 , pp. 88-95
    • Chin, F.T.1    Shen, B.2    Liu, S.L.3
  • 25
    • 84877728996 scopus 로고    scopus 로고
    • RGD-based PET tracers for imaging receptor integrin alphavbeta3 expression
    • Cai H, Conti PS. RGD-based PET tracers for imaging receptor integrin alphavbeta3 expression. J Labelled Comp Radiopharm. 2013;56:264-279.
    • (2013) J Labelled Comp Radiopharm , vol.56 , pp. 264-279
    • Cai, H.1    Conti, P.S.2
  • 26
    • 78650412005 scopus 로고    scopus 로고
    • One-step F-18-labeling of carbohydrateconjugated octreotate-derivatives containing a silicon-fluoride-acceptor (SiFA): In vitro and in vivo evaluation as tumor imaging agents for positron emission tomography (PET)
    • Wängler C, Waser B, Alke A, et al. One-step F-18-labeling of carbohydrateconjugated octreotate-derivatives containing a silicon-fluoride-acceptor (SiFA): in vitro and in vivo evaluation as tumor imaging agents for positron emission tomography (PET). Bioconjug Chem. 2010;21:2289-2296.
    • (2010) Bioconjug Chem , vol.21 , pp. 2289-2296
    • Wängler, C.1    Waser, B.2    Alke, A.3
  • 27
    • 84860271819 scopus 로고    scopus 로고
    • Optimized labeling of NOTA-conjugated octreotide with F-18
    • Laverman P, D'Souza CA, Eek A, et al. Optimized labeling of NOTA-conjugated octreotide with F-18. Tumour Biol. 2012;33:427-434.
    • (2012) Tumour Biol , vol.33 , pp. 427-434
    • Laverman, P.1    D'souza, C.A.2    Eek, A.3
  • 28
    • 77950348936 scopus 로고    scopus 로고
    • A novel facile method of labeling octreotide with F-18-fluorine
    • Laverman P, McBride WJ, Sharkey RM, et al. A novel facile method of labeling octreotide with F-18-fluorine. J Nucl Med. 2010;51:454-461.
    • (2010) J Nucl Med , vol.51 , pp. 454-461
    • Laverman, P.1    McBride, W.J.2    Sharkey, R.M.3
  • 29
    • 84872847401 scopus 로고    scopus 로고
    • 18F-labeling of an aryltrifluoroborate bioconjugate by isotope exchange at very high specific activity
    • Liu Z, Li Y, Lozada J, et al. Rapid, one-step, high yielding 18F-labeling of an aryltrifluoroborate bioconjugate by isotope exchange at very high specific activity. J Labelled Comp Radiopharm. 2012;14:491-497.
    • (2012) J Labelled Comp Radiopharm , vol.14 , pp. 491-497
    • Liu, Z.1    Li, Y.2    Lozada, J.3
  • 30
    • 84881031050 scopus 로고    scopus 로고
    • 18F-labeling of RGD-19F-arytrifluroborate in high yield and at extraordinarily high specific activity with preliminary in vivo tumor imaging
    • Liu Z, Li Y, Lozada J, et al. Kit-like 18F-labeling of RGD-19F-arytrifluroborate in high yield and at extraordinarily high specific activity with preliminary in vivo tumor imaging. Nucl Med Biol. 2013;40:841-849.
    • (2013) Nucl Med Biol , vol.40 , pp. 841-849
    • Liu, Z.1    Li, Y.2    Lozada, J.3
  • 31
    • 84873917554 scopus 로고    scopus 로고
    • 18F-aryltrifluoroborate radiosynthesis at high specific activity for click conjugation
    • Liu Z, Li Y, Lozada J, et al. Stoichiometric leverage: rapid 18F-aryltrifluoroborate radiosynthesis at high specific activity for click conjugation. Angew Chem Int Ed. 2013;52:2305-2307.
    • (2013) Angew Chem Int Ed , vol.52 , pp. 2305-2307
    • Liu, Z.1    Li, Y.2    Lozada, J.3
  • 32
    • 0033119067 scopus 로고    scopus 로고
    • 3-octreotate: A new somatostatin analog with improved target tissue uptake
    • Lewis JS, Srinivasan A, Schmidt MA, Anderson CJ. In vitro and in vivo evaluation of Cu-64-TETA-Tyr3-octreotate: a new somatostatin analog with improved target tissue uptake. Nucl Med Biol. 1999;26:267-273.
    • (1999) Nucl Med Biol , vol.26 , pp. 267-273
    • Lewis, J.S.1    Srinivasan, A.2    Schmidt, M.A.3    Anderson, C.J.4
  • 33
    • 0000504238 scopus 로고
    • Iodomethaneboronic esters and aminomethane boronic esters
    • Matteson DS, Majumdar D. Iodomethaneboronic esters and aminomethane boronic esters. J Organomet Chem. 1979;170:259-264.
    • (1979) J Organomet Chem , vol.170 , pp. 259-264
    • Matteson, D.S.1    Majumdar, D.2
  • 34
    • 84860198687 scopus 로고    scopus 로고
    • -production
    • Eberl S, Eriksson T, Svedberg O, et al. High beam current operation of a PETtrace™ cyclotron for 18F- production. Appl Radiat Isot. 2012;70:922-930.
    • (2012) Appl Radiat Isot , vol.70 , pp. 922-930
    • Eberl, S.1    Eriksson, T.2    Svedberg, O.3
  • 35
    • 84866184119 scopus 로고    scopus 로고
    • Unexpected sensitivity of sst2 antagonists to N-terminal radiometal modifications
    • Fani M, Braun F, Waser B, et al. Unexpected sensitivity of sst2 antagonists to N-terminal radiometal modifications. J Nucl Med. 2012;53:1481-1489.
    • (2012) J Nucl Med , vol.53 , pp. 1481-1489
    • Fani, M.1    Braun, F.2    Waser, B.3
  • 36
    • 0034033495 scopus 로고    scopus 로고
    • Affinity profiles for human somatostatin receptor subtypes SST1-SST5 of somatostatin radiotracers selected for scintigraphic and radiotherapeutic use
    • Reubi JC, Schar JC, Waser B, et al. Affinity profiles for human somatostatin receptor subtypes SST1-SST5 of somatostatin radiotracers selected for scintigraphic and radiotherapeutic use. Eur J Nucl Med. 2000;27:273-282.
    • (2000) Eur J Nucl Med , vol.27 , pp. 273-282
    • Reubi, J.C.1    Schar, J.C.2    Waser, B.3
  • 37
    • 0030161551 scopus 로고    scopus 로고
    • Preclinical evaluation of technetium-99m-labeled somatostatin receptor-binding peptides
    • Vallabhajosula S, Moyer BR, Lister-James J, et al. Preclinical evaluation of technetium-99m-labeled somatostatin receptor-binding peptides. J Nucl Med. 1996;37:1016-1022.
    • (1996) J Nucl Med , vol.37 , pp. 1016-1022
    • Vallabhajosula, S.1    Moyer, B.R.2    Lister-James, J.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.