Skip to main content
Erschienen in: European Journal of Nuclear Medicine and Molecular Imaging 7/2006

01.07.2006 | Original article

Quantitative assessment of SSTR2 expression in patients with non-small cell lung cancer using68Ga-DOTATOC PET and comparison with18F-FDG PET

verfasst von: Antonia Dimitrakopoulou-Strauss, Vassilios Georgoulias, Michael Eisenhut, Felix Herth, Sophia Koukouraki, Helmut R. Mäcke, Uwe Haberkorn, Ludwig G. Strauss

Erschienen in: European Journal of Nuclear Medicine and Molecular Imaging | Ausgabe 7/2006

Einloggen, um Zugang zu erhalten

Abstract

Purpose

Dynamic PET studies with68Ga-DOTATOC were performed in patients with non-small cell lung cancer (NSCLC) to assess the somatostatin receptor 2 (SSTR2) expression. Furthermore, dynamic18F-fluorodeoxyglucose (FDG) studies were performed in the same patients to compare the SSTR2 expression with the tumour viability.

Methods

The study population comprised nine patients, examined with both tracers on two different days within 1 week. Standardised uptake values (SUVs) were calculated and a two-tissue compartment model was applied to the data. Furthermore, a non-compartment model based on the fractal dimension (FD) was applied to the data.

Results

The DOTATOC uptake was generally lower than the FDG uptake. Moderately enhanced DOTATOC uptake was noted in seven of the nine tumours. All kinetic parameters exceptk 4 were lower for DOTATOC than for FDG. The mean SUV was 2.018 for DOTATOC, in comparison to 5.683 for FDG. In particular,k 3 was highly variable for DOTATOC and showed an overlap with the normal lung tissue. The fractional blood volumeV B was relatively low for both tracers, not exceeding 0.3. The highest significant logarithmic correlation was found for the FD of the two tracers (r=0.764,p=0.017). The logarithmic correlation for SUVs was also significant (r=0.646,p=0.060), as was that forV B (r=0.629,p=0.069). In contrast, none of the eight metastases which were positive on FDG PET showed any DOTATOC uptake.

Conclusion

The results demonstrated moderate68Ga-DOTATOC uptake in primary NSCLC but did not provide any evidence for SSTR2 expression in metastases. This may be caused by loss of the gene expression in metastases as compared with the primary tumours.
Literatur
1.
Zurück zum Zitat Mena E, Camacho V, Estorch M, Fuertes J, Flotats A, Carrió I.99mTc-depreotide scintigraphy of bone lesions in patients with lung cancer. Eur J Nucl Med Mol Imaging 2004;31:1399–1404CrossRefPubMed Mena E, Camacho V, Estorch M, Fuertes J, Flotats A, Carrió I.99mTc-depreotide scintigraphy of bone lesions in patients with lung cancer. Eur J Nucl Med Mol Imaging 2004;31:1399–1404CrossRefPubMed
2.
Zurück zum Zitat Szereday Z, Schally AV, Szepeshazi K, Bajo AM, Hebert F, Halmos G, et al. Effective treatment of H838 human non-small cell lung carcinoma with a targeted cytotoxic somatostatin analog, AN-238. Int J Oncol 2003;22:1141–1146PubMed Szereday Z, Schally AV, Szepeshazi K, Bajo AM, Hebert F, Halmos G, et al. Effective treatment of H838 human non-small cell lung carcinoma with a targeted cytotoxic somatostatin analog, AN-238. Int J Oncol 2003;22:1141–1146PubMed
3.
Zurück zum Zitat Bohuslavizki KH, Brenner W, Braunsdorf WE, Behnke A, Tinnemeyer S, Hugo HH, et al. Somatostatin receptor scintigraphy in the differential diagnosis of meningioma. Nucl Med Commun 1996;17:302–310PubMedCrossRef Bohuslavizki KH, Brenner W, Braunsdorf WE, Behnke A, Tinnemeyer S, Hugo HH, et al. Somatostatin receptor scintigraphy in the differential diagnosis of meningioma. Nucl Med Commun 1996;17:302–310PubMedCrossRef
4.
Zurück zum Zitat Heppeler A, Froidevaux S, Mäcke HR, Jermann E, Béhé M, Powell P, et al. Radiometal-labelled macrocyclic chelator-derivatised somatostatin analogue with superb tumor-targeting properties and potential for receptor-mediated internal radiotherapy. Chem Eur J 1999;7:1974–1981CrossRef Heppeler A, Froidevaux S, Mäcke HR, Jermann E, Béhé M, Powell P, et al. Radiometal-labelled macrocyclic chelator-derivatised somatostatin analogue with superb tumor-targeting properties and potential for receptor-mediated internal radiotherapy. Chem Eur J 1999;7:1974–1981CrossRef
5.
Zurück zum Zitat Strauss LG, Conti PS. The applications of PET in clinical oncology. J Nucl Med 1991;32:623–648PubMed Strauss LG, Conti PS. The applications of PET in clinical oncology. J Nucl Med 1991;32:623–648PubMed
6.
Zurück zum Zitat Burger C, Buck A. Requirements and implementations of a flexible kinetic modeling tool. J Nucl Med 1997;38:1818–1823PubMed Burger C, Buck A. Requirements and implementations of a flexible kinetic modeling tool. J Nucl Med 1997;38:1818–1823PubMed
7.
Zurück zum Zitat Mikolajczyk K, Szabatin M, Rudnicki P, Grodzki M, Burger C. A Java environment for medical image data analysis: initial application for brain PET quantitation. Med Inform 1998;23:207–214 Mikolajczyk K, Szabatin M, Rudnicki P, Grodzki M, Burger C. A Java environment for medical image data analysis: initial application for brain PET quantitation. Med Inform 1998;23:207–214
8.
Zurück zum Zitat Miyazawa H, Osmont A, Petit-Taboue MC, Tillet I, Travere JM, Young AR, et al. Determination of18F-fluoro-2-deoxy-D-glucose rate constants in the anesthetized baboon brain with dynamic positron tomography. J Neurosci Methods 1993;50:263–272CrossRefPubMed Miyazawa H, Osmont A, Petit-Taboue MC, Tillet I, Travere JM, Young AR, et al. Determination of18F-fluoro-2-deoxy-D-glucose rate constants in the anesthetized baboon brain with dynamic positron tomography. J Neurosci Methods 1993;50:263–272CrossRefPubMed
9.
Zurück zum Zitat Sokoloff L, Smith CB. Basic principles underlying radioisotopic methods for assay of biochemical processes in vivo. In: Greitz T, Ingvar DH, Widén L, editors. The metabolism of the human brain studied with positron emission tomography. New York: Raven Press; 1983; p.123–148 Sokoloff L, Smith CB. Basic principles underlying radioisotopic methods for assay of biochemical processes in vivo. In: Greitz T, Ingvar DH, Widén L, editors. The metabolism of the human brain studied with positron emission tomography. New York: Raven Press; 1983; p.123–148
10.
Zurück zum Zitat Ohtake T, Kosaka N, Watanabe T, Yokoyama I, Moritan T, Masuo M, et al. Noninvasive method to obtain input function for measuring glucose utilization of thoracic and abdominal organs. J Nucl Med 1991;32:1432–1438PubMed Ohtake T, Kosaka N, Watanabe T, Yokoyama I, Moritan T, Masuo M, et al. Noninvasive method to obtain input function for measuring glucose utilization of thoracic and abdominal organs. J Nucl Med 1991;32:1432–1438PubMed
11.
Zurück zum Zitat Dimitrakopoulou-Strauss A, Strauss LG, Burger C, Mikolajczyk K, Lehnert T, Bernd L, et al. On the fractal nature of dynamic positron emission tomography (PET) studies. World J Nucl Med 2003;2:306–313 Dimitrakopoulou-Strauss A, Strauss LG, Burger C, Mikolajczyk K, Lehnert T, Bernd L, et al. On the fractal nature of dynamic positron emission tomography (PET) studies. World J Nucl Med 2003;2:306–313
12.
Zurück zum Zitat Kelly RF, Tran T, Holmstrom A, Murar J, Segurola RJ Jr. Accuracy and cost-effectiveness of (18F)-2-fluoro-deoxy-D-glucose-positron emission tomography scan in potentially resectable non-small cell lung cancer. Chest 2004;125:1413–1423CrossRefPubMed Kelly RF, Tran T, Holmstrom A, Murar J, Segurola RJ Jr. Accuracy and cost-effectiveness of (18F)-2-fluoro-deoxy-D-glucose-positron emission tomography scan in potentially resectable non-small cell lung cancer. Chest 2004;125:1413–1423CrossRefPubMed
13.
Zurück zum Zitat Dwamena BA, Sonnad SS, Angobaldo JO, Wahl RL. Metastases from non-small cell lung cancer: mediastinal staging in the 1990s—meta-analytic comparison of PET and CT. Radiology 1999;213:530–536PubMed Dwamena BA, Sonnad SS, Angobaldo JO, Wahl RL. Metastases from non-small cell lung cancer: mediastinal staging in the 1990s—meta-analytic comparison of PET and CT. Radiology 1999;213:530–536PubMed
14.
Zurück zum Zitat Fujita T, Yamaji Y, Sato M, Murao K, Takahara J. Gene expression of somatostatin receptor subtypes, SSTR 1 and SSTR 2, in human lung cancer cell lines. Life Sci 1994;55:1797–1806CrossRefPubMed Fujita T, Yamaji Y, Sato M, Murao K, Takahara J. Gene expression of somatostatin receptor subtypes, SSTR 1 and SSTR 2, in human lung cancer cell lines. Life Sci 1994;55:1797–1806CrossRefPubMed
15.
Zurück zum Zitat Blum J, Handmaker H, Lister-James J, Rinne N. A multicenter trial with a somatostatin analog99mTc depreotide in the evaluation of solitary pulmonary nodules. Chest 2000;117:1232–1238CrossRefPubMed Blum J, Handmaker H, Lister-James J, Rinne N. A multicenter trial with a somatostatin analog99mTc depreotide in the evaluation of solitary pulmonary nodules. Chest 2000;117:1232–1238CrossRefPubMed
16.
Zurück zum Zitat Kahn D, Menda Y, Kernstine K, Bushnell D, McLaughlin K, Miller S, et al The utility of99mTc depreotide compared with F-18-fluorodeoxyglucose positron emission tomography and surgical staging in patients with suspected non-small cell lung cancer. Chest 2004;125:494–501CrossRefPubMed Kahn D, Menda Y, Kernstine K, Bushnell D, McLaughlin K, Miller S, et al The utility of99mTc depreotide compared with F-18-fluorodeoxyglucose positron emission tomography and surgical staging in patients with suspected non-small cell lung cancer. Chest 2004;125:494–501CrossRefPubMed
17.
Zurück zum Zitat Henze M, Dimitrakopoulou-Strauss A, Milker-Zabel S, Schuhmacher J, Strauss LG, Doll J, et al Characterization of 68Ga-DOTA-D-Phe1-Tyr3-octreotide (DOTA-TOC) kinetics in patients with meningiomas. J Nucl Med 2005;46:763–769PubMed Henze M, Dimitrakopoulou-Strauss A, Milker-Zabel S, Schuhmacher J, Strauss LG, Doll J, et al Characterization of 68Ga-DOTA-D-Phe1-Tyr3-octreotide (DOTA-TOC) kinetics in patients with meningiomas. J Nucl Med 2005;46:763–769PubMed
18.
Zurück zum Zitat Koukouraki S, Strauss LG, Georgoulias V, Schuhmacher J, Haberkorn U, Karkavitsas N, et al. Pharmacokinetic studies of 68Ga-DOTATOC PET in patients with metastatic neuroendocrine tumours planned for 90Y-DOTATOC therapy. Eur J Nucl Med Mol Imaging 2006 Jan 17:1–7 [Epub ahead of print]. DOI 10.1007/s00259-005-0006-1 Koukouraki S, Strauss LG, Georgoulias V, Schuhmacher J, Haberkorn U, Karkavitsas N, et al. Pharmacokinetic studies of 68Ga-DOTATOC PET in patients with metastatic neuroendocrine tumours planned for 90Y-DOTATOC therapy. Eur J Nucl Med Mol Imaging 2006 Jan 17:1–7 [Epub ahead of print]. DOI 10.1007/s00259-005-0006-1
19.
Zurück zum Zitat Dimitrakopoulou-Strauss A, Strauss LG, Burger C. Quantitative PET studies in pretreated melanoma patients: a comparison of 6-(18F)-fluoro-L-dopa with 18F-FDG and 15O-water using compartment and noncompartment analysis. J Nucl Med 2001;42:248–256PubMed Dimitrakopoulou-Strauss A, Strauss LG, Burger C. Quantitative PET studies in pretreated melanoma patients: a comparison of 6-(18F)-fluoro-L-dopa with 18F-FDG and 15O-water using compartment and noncompartment analysis. J Nucl Med 2001;42:248–256PubMed
Metadaten
Titel
Quantitative assessment of SSTR2 expression in patients with non-small cell lung cancer using68Ga-DOTATOC PET and comparison with18F-FDG PET
verfasst von
Antonia Dimitrakopoulou-Strauss
Vassilios Georgoulias
Michael Eisenhut
Felix Herth
Sophia Koukouraki
Helmut R. Mäcke
Uwe Haberkorn
Ludwig G. Strauss
Publikationsdatum
01.07.2006
Verlag
Springer-Verlag
Erschienen in
European Journal of Nuclear Medicine and Molecular Imaging / Ausgabe 7/2006
Print ISSN: 1619-7070
Elektronische ISSN: 1619-7089
DOI
https://doi.org/10.1007/s00259-005-0063-5

Weitere Artikel der Ausgabe 7/2006

European Journal of Nuclear Medicine and Molecular Imaging 7/2006 Zur Ausgabe