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The Relationship between FDG Uptake in PET Scans and Biological Behavior in Breast Cancer

机译:PET扫描中FDG摄取与乳腺癌生物学行为之间的关系

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Background: Positron emission tomography (PET) is a non-invasive imaging modality used in the diagnosis and staging of breast cancer. However, several factors can affect fluoro-deoxyglucose (FDG) uptake by a tumor. To clarify the parameters that most affect FDG accumulation in tumors, the relationship between standardized uptake values (SUVs) and clinicopathological factors and immunohistopathological analysis was investigated in breast cancer.Material and Methods: PET studies were performed preoperatively on 37 patients with breast carcinoma. SUVs were counted at one hour (early phase) and at two hours (delayed phase) after FDG injection. The relationships between SUVs and 13 clinical, pathological and immunohistchemical factors were studied.Results: A significant association was found between FDG accumulation and early and delayed phase mitotic counts (p=0.0018 and 0.0010, respectively), Ki67 positive cell percentage (p=0.0098 and 0.0062, respectively), and nuclear grade (p=0.0232 and 0.0195, respectively). On the other hand, nodal status weakly correlated with the delayed phase (p=0.0907). However, other clinicopathological parameters and immunohistopathological status, which included tumor size, age, histology, estrogen receptor, progesterone receptor and Her2eu overexpression, did not correlate significantly with FDG uptake.Conclusion: Mitotic count and Ki67 reflect cellular aggressiveness. These parameters were strongly correlated with tracer uptake. Thus our data suggested that the biological behavior of breast cancer is reflected in the variation of FDG uptake by the tumor. However, whether FDG uptake is a true prognostic and predictive factor remains to be confirmed in larger studies over an extended period of time.
机译:背景:正电子发射断层扫描(PET)是一种用于乳腺癌的诊断和分期的非侵入性成像方式。但是,有几个因素会影响肿瘤吸收氟脱氧葡萄糖(FDG)。为了弄清影响肿瘤中FDG积累的参数,研究了标准摄取值(SUVs)与临床病理因素之间的关系以及免疫组织病理学分析。材料与方法:术前对37例乳腺癌患者进行了PET研究。在注入FDG后的一小时(早期)和两小时(延迟阶段)对SUV进行计数。研究了SUVs与13种临床,病理和免疫组化因子之间的关系。结果:发现FDG积累与早期和延迟期有丝分裂计数(分别为p = 0.0018和0.0010),Ki67阳性细胞百分比(p = 0.0098)之间存在显着相关性分别为0.0062和0.0062)和核级(分别为p = 0.0232和0.0195)。另一方面,节点状态与延迟相位弱相关(p = 0.0907)。然而,其他临床病理学参数和免疫组织病理学状态,包括肿瘤大小,年龄,组织学,雌激素受体,孕激素受体和Her2 / neu过表达,与FDG摄取均无显着相关。这些参数与示踪剂摄取高度相关。因此,我们的数据表明,乳腺癌的生物学行为反映在肿瘤摄取FDG的变化中。但是,FDG摄取是否是真正的预后和预测因素,仍需在较大的研究范围内进行确认。

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