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Molecular Whole-Body Cancer Staging Using Positron Emission Tomography: Consequences for Therapeutic Management and Metabolic Radiation Treatment Planning

机译:使用正电子发射断层扫描的分子全身癌症分期:治疗管理和代谢辐射治疗计划的后果

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A prospective analysis was performed in 124 non-small cell lung cancer patients to determine the role of F-18 fluorodeoxyglucose (FDG)-positron emission tomography (PET) for molecular (metabolic) staging (n=63), therapy monitoring after induction-chemotherapy (n=34), and conformal radiation treatment planning (n=27). Staging by FDG-PET was significantly more accurate than CT (p<0.001) and changed therapeutic management in 52% of all patients. After induction-chemotherapy, patients with complete metabolic remission histologically did not show vital tumor cells in contrast to patients with metabolic partial remission or progressive disease. Metabolic radiation treatment planning by PET led to smaller planning target volumes (PTVs) for radiation therapy (between 3% and 21% in 25/27 patients), resulting in a reduction of dose exposure to healthy tissue. In two patients, PET-PTV was larger than CT-based PTV, since PET detected lymph node metastases smaller than 1 cm. FDG-PET provides clinically important information; changes therapeutic management, can predict noninvasively effectiveness of chemotherapy, and may lead to better tumor control with less radiation-induced toxicity.
机译:在124非小细胞肺癌患者进行,以确定F-18氟代脱氧葡萄糖(FDG)-positron发射断层扫描(PET),用于分子(代谢)的分段作用的前瞻性分析(N = 63),治疗后监测感应 - 化疗(n = 34)和保形辐射治疗计划(n = 27)。 FDG-PET分期比CT(P <0.001)更准确,并在所有患者的52%中改变治疗管理。诱导化疗后,患有完全代谢缓解的患者组织学上没有表现出与代谢部分缓解或渐进性疾病的患者相比表现出生命的肿瘤细胞。 PET的代谢辐射治疗计划导致较小的规划目标体积(PTV)用于放射治疗(25/27名患者的3%和21%),导致剂量暴露于健康组织。在两名患者中,PET-PTV大于基于CT的PTV,因为PET检测到小于1cm的淋巴结转移。 FDG-PET提供临床重要信息;改变治疗管理,可以预测化疗的非侵略性有效性,并且可能导致更好的肿瘤控制,较少的辐射诱导的毒性。

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