Quantitative assessment of SSTR2 expression in patients with non-small cell lung cancer using68Ga-DOTATOC PET and comparison with18F-FDG PET
Creators
- 1. German Cancer Research Center, Medical PET Group - Biological Imaging (E0601) Clinical Cooperation Unit Nuclear Medicine, Heidelberg (Germany)
- 2. University of Crete, Department of Medical Oncology, Herakleion (Greece)
- 3. German Cancer Research Center, Department of Radiopharmaceutical Chemistry, Heidelberg (Germany)
- 4. University of Heidelberg, Department of Pulmonology, Thoraxklinik Rohrbach, Heidelberg (Germany)
- 5. University of Crete, Department of Nuclear Medicine, Herakleion (Greece)
- 6. University Hospital Basel, Division of Radiological Chemistry, Department of Radiology, Basel (Switzerland)
- 7. University of Heidelberg, Department of Nuclear Medicine, Heidelberg (Germany)
Description
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. 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. 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 exceptk4 were lower for DOTATOC than for FDG. The mean SUV was 2.018 for DOTATOC, in comparison to 5.683 for FDG. In particular,k3 was highly variable for DOTATOC and showed an overlap with the normal lung tissue. The fractional blood volumeVB 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 forVB (r=0.629,p=0.069). In contrast, none of the eight metastases which were positive on FDG PET showed any DOTATOC uptake. 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. (orig.)
Availability note (English)
Available from: http://dx.doi.org/10.1007/s00259-005-0063-5Additional details
Identifiers
Publishing Information
- Journal Title
- European Journal of Nuclear Medicine and Molecular Imaging
- Journal Volume
- 33
- Journal Issue
- 7
- Journal Page Range
- p. 823-830
- ISSN
- 1619-7070
INIS
- Country of Publication
- Germany
- Country of Input or Organization
- Germany
- INIS RN
- 37105528
- Subject category
- S62: RADIOLOGY AND NUCLEAR MEDICINE;
- Descriptors DEI
- CARCINOMAS; FLUORINE 18; FLUORODEOXYGLUCOSE; LUNGS; POSITRON COMPUTED TOMOGRAPHY; TUMOR CELLS
- Descriptors DEC
- ANIMAL CELLS; ANTIMETABOLITES; BETA DECAY RADIOISOTOPES; BETA-PLUS DECAY RADIOISOTOPES; BODY; COMPUTERIZED TOMOGRAPHY; DIAGNOSTIC TECHNIQUES; DISEASES; DRUGS; EMISSION COMPUTED TOMOGRAPHY; FLUORINE ISOTOPES; HOURS LIVING RADIOISOTOPES; ISOMERIC TRANSITION ISOTOPES; ISOTOPES; LIGHT NUCLEI; NANOSECONDS LIVING RADIOISOTOPES; NEOPLASMS; NUCLEI; ODD-ODD NUCLEI; ORGANS; RADIOISOTOPES; RESPIRATORY SYSTEM; TOMOGRAPHY