Department of Nuclear Medicine, Konkuk University Medical Center, Konkuk University School of Medicine, 4-12 Hwayang-dong, Kwangjin-gu, Seoul, Korea.
J Cancer Res Clin Oncol. 2010 Dec;136(12):1929-35. doi: 10.1007/s00432-010-0852-5. Epub 2010 Mar 20.
We evaluated the role of FDG-PET/CT in patients with metastatic gastric adenocarcinoma before palliative chemotherapy to predict prognosis and chemotherapeutic response.
The study included 35 consecutive newly diagnosed patients with metastatic gastric adenocarcinoma who underwent FDG-PET/CT before palliative chemotherapy. Maximum standardized uptake value (SUVmax) of the primary tumor was assessed to evaluate survival and chemotherapeutic response. Survival analysis was performed for time to progression and overall survival using the Kaplan-Meier method. Cox proportional hazard models were used to determine independent prognostic factors.
All primary tumors were visualized using FDG-PET/CT (mean SUVmax = 8.1 ± 4.5, range 2.5-22.1). Sensitivity, specificity, and accuracy of FDG-PET/CT in detection of solid organ metastasis were 95.2% (20/21), 100% (14/14), and 97.1% (34/35), respectively. No significant difference of primary tumor SUVmax was found among the chemotherapeutic response groups. Univariate survival analysis demonstrated ECOG performance status (≥2), presence of solid organ metastasis, number of organs involved in distant metastasis (≥2), and SUVmax of the primary tumor (>8) as significant predictors for poor overall survival. Multivariate survival analysis showed SUVmax of the primary tumor (P = 0.048), presence of solid organ metastasis (P = 0.015), and ECOG performance status (P = 0.002) as significant independent prognostic predictors for overall survival.
High FDG uptake of the primary tumor in patients with metastatic gastric adenocarcinoma is associated with poor overall survival. Assessment of tumor FDG uptake has limited value for prediction of chemotherapeutic response, but provides useful information regarding prognosis.
我们评估了 FDG-PET/CT 在接受姑息性化疗的转移性胃腺癌患者中的作用,以预测预后和化疗反应。
这项研究纳入了 35 例新诊断的转移性胃腺癌患者,这些患者在姑息性化疗前接受了 FDG-PET/CT 检查。评估原发肿瘤的最大标准化摄取值(SUVmax),以评估生存和化疗反应。使用 Kaplan-Meier 方法进行无进展生存期和总生存期的生存分析。使用 Cox 比例风险模型确定独立的预后因素。
所有原发肿瘤均通过 FDG-PET/CT 显影(平均 SUVmax=8.1±4.5,范围 2.5-22.1)。FDG-PET/CT 检测实体器官转移的灵敏度、特异性和准确性分别为 95.2%(20/21)、100%(14/14)和 97.1%(34/35)。化疗反应组之间原发肿瘤 SUVmax 无显著差异。单因素生存分析表明,ECOG 表现状态(≥2)、存在实体器官转移、远处转移涉及的器官数(≥2)和原发肿瘤 SUVmax(>8)是总生存期不良的显著预测因素。多因素生存分析显示,原发肿瘤 SUVmax(P=0.048)、存在实体器官转移(P=0.015)和 ECOG 表现状态(P=0.002)是总生存期的独立预后预测因素。
转移性胃腺癌患者原发肿瘤的高 FDG 摄取与总生存期不良相关。肿瘤 FDG 摄取的评估对预测化疗反应的价值有限,但对预后提供了有用的信息。