Dimitrakopoulou-Strauss Antonia, Georgoulias Vassilios, Eisenhut Michael, Herth Felix, Koukouraki Sophia, Mäcke Helmut R, Haberkorn Uwe, Strauss Ludwig G
Medical PET Group--Biological Imaging (E0601), Clinical Cooperation Unit, Nuclear Medicine, German Cancer Research Center, Im Neuenheimer Feld 280, 69120 Heidelberg, Germany.
Eur J Nucl Med Mol Imaging. 2006 Jul;33(7):823-30. doi: 10.1007/s00259-005-0063-5. Epub 2006 Mar 29.
Dynamic PET studies with(68)Ga-DOTATOC were performed in patients with non-small cell lung cancer (NSCLC) to assess the somatostatin receptor 2 (SSTR2) expression. Furthermore, dynamic(18)F-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 except k (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 volume V (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.
The results demonstrated moderate (68)Ga-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.
对非小细胞肺癌(NSCLC)患者进行(68)Ga - DOTATOC动态PET研究,以评估生长抑素受体2(SSTR2)的表达。此外,对同一批患者进行动态(18)F - 氟脱氧葡萄糖(FDG)研究,以比较SSTR2表达与肿瘤活性。
研究人群包括9名患者,在1周内的不同两天用两种示踪剂进行检查。计算标准化摄取值(SUV),并将双组织室模型应用于数据。此外,基于分形维数(FD)的非室模型也应用于数据。
DOTATOC摄取通常低于FDG摄取。9个肿瘤中有7个观察到DOTATOC摄取适度增强。除k(4)外,DOTATOC的所有动力学参数均低于FDG。DOTATOC的平均SUV为2.018,而FDG为5.683。特别是,DOTATOC的k(3)变化很大,与正常肺组织有重叠。两种示踪剂的分数血容量V(B)相对较低,不超过0.3。两种示踪剂的FD之间发现最高的显著对数相关性(r = 0.764,p = 0.017)。SUV的对数相关性也显著(r = 0.646,p = 0.060),V(B)的对数相关性也是如此(r = 0.629,p = 0.069)。相比之下,FDG PET阳性的8个转移灶均未显示任何DOTATOC摄取。
结果表明原发性NSCLC中(68)Ga - DOTATOC摄取适度,但没有提供转移灶中SSTR2表达的任何证据。这可能是由于与原发性肿瘤相比,转移灶中基因表达缺失所致。