Andersen Kim Francis, Skougaard Kristin, Nielsen Anne Lerberg, Hendel Helle Westergren
Department of Clinical Physiology and Nuclear Medicine, Herlev Hospital, DK-2730 Herlev.
Oncol Lett. 2012 Jul;4(1):131-134. doi: 10.3892/ol.2012.683. Epub 2012 Apr 18.
The correct interpretation of metabolic response in cancer cells to therapy requires knowledge of how tumor-free tissue responds to the same treatment. The aim of this study was to evaluate standardized uptake values (SUVs) in tumor-free regions of patients with metastatic colorectal cancer prior to and following therapy, via the use of 18-fluoride fluoro-2-deoxy-D-glucose (18F-FDG) positron emission tomography/computed tomography (PET/CT). On baseline 18F-FDG PET/CT scans (n=51), volumes of interest (VOI) were obtained from tumor-free tissue (aortic arch, liver and spleen) and SUVs normalized to total body mass were registered. The procedure was repeated for a follow-up scan two weeks following a single administration of the third-line treatment with irinotecan plus cetuximab. The mean differences in SUV prior to and following therapy were non-significant (P>0.05) in all the registered tumor-free regions. Correlation coefficients indicated a significant result between the variables (0.74-0.84; P<0.001). This study suggests that the early assessment of metabolic response may be made following the administration of third-line therapy with irinotecan plus cetuximab in patients with metastatic colorectal cancer refractory to second-line treatment with irinotecan.
正确解读癌细胞对治疗的代谢反应需要了解无瘤组织对相同治疗的反应情况。本研究的目的是通过使用18氟氟代2脱氧-D-葡萄糖(18F-FDG)正电子发射断层扫描/计算机断层扫描(PET/CT),评估转移性结直肠癌患者在治疗前后无瘤区域的标准化摄取值(SUV)。在基线18F-FDG PET/CT扫描(n = 51)中,从无瘤组织(主动脉弓、肝脏和脾脏)获取感兴趣体积(VOI),并记录归一化至总体重的SUV。在单次给予伊立替康加西妥昔单抗进行三线治疗两周后进行随访扫描时重复该操作。在所有记录的无瘤区域中,治疗前后SUV的平均差异无统计学意义(P>0.05)。相关系数表明变量之间存在显著结果(0.74 - 0.84;P<0.001)。本研究表明,对于二线治疗用伊立替康难治的转移性结直肠癌患者,在给予伊立替康加西妥昔单抗进行三线治疗后,可能可以进行代谢反应的早期评估。