首页> 外文期刊>International Journal of Radiation Oncology, Biology, Physics >Correlation between radiation dose to 18F-FDG-PET defined active bone marrow subregions and acute hematologic toxicity in cervical cancer patients treated with chemoradiotherapy
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Correlation between radiation dose to 18F-FDG-PET defined active bone marrow subregions and acute hematologic toxicity in cervical cancer patients treated with chemoradiotherapy

机译:放化疗对子宫颈癌患者放射剂量至18F-FDG-PET定义的活动性骨髓亚区域与急性血液学毒性的相关性

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Purpose: To test the hypothesis that radiation dose to 18F- fluorodeoxyglucose positron emission tomography ( 18F-FDG-PET)-defined active bone marrow (BM ACT) subregions is correlated with hematologic toxicity in cervical cancer patients treated with chemoradiotherapy. Methods and Materials: The conditions of 26 women with cervical cancer who underwent 18F-FDG-PET before treatment with concurrent cisplatin and intensity-modulated radiation therapy were analyzed. BM ACT was defined as the subregion of total bone marrow (BM TOT) with a standardized uptake value (SUV) equal to or above the mean for that individual. Inactive bone marrow (BM INACT) was defined as BM TOT - BM ACT. Generalized linear modeling was used to test the correlation between BM ACT and BM INACT dose-volume metrics and hematologic nadirs, particularly white blood cell count (WBC) and absolute neutrophil count (ANC). Results: Increased BM ACT mean dose was significantly associated with decreased log(WBC) nadir (β = -0.04; 95% CI, -0.07to -0.01; p = 0.009), decreased log(ANC) nadir (β = -0.05; 95% CI, -0.08 to -0.02; p = 0.006), decreased hemoglobin nadir (β = -0.16; 95% CI, -0.27 to -0.05; p = 0.010), and decreased platelet nadir (β = -6.16; 95% CI, -9.37 to -2.96; p 0.001). By contrast, there was no association between BM INACT mean dose and log(WBC) nadir (β = -0.01; 95% CI, -0.06 to 0.05; p = 0.84), log(ANC) nadir (β = -0.03; 95% CI, -0.10 to 0.04; p = 0.40), hemoglobin nadir (β = -0.09; 95% CI, -0.31 to 0.14; p = 0.452), or platelet nadir (β = -3.47; 95% CI, -10.44 to 3.50; p = 0.339). Conclusions: Irradiation of BM subregions with higher 18F-FDG-PET activity was associated with hematologic toxicity, supporting the hypothesis that reducing dose to BM ACT subregions could mitigate hematologic toxicity. Future investigation should seek to confirm these findings and to identify optimal SUV thresholds to define BM ACT.
机译:目的:为了检验以下假设:在接受放化疗的宫颈癌患者中,18F-氟脱氧葡萄糖正电子发射断层扫描(18F-FDG-PET)定义的活性骨髓(BM ACT)子区域的辐射剂量与血液学毒性相关。方法和材料:分析了26例宫颈癌女性患者的病情,这些女性患者在同时进行顺铂和强度调节放射治疗之前接受了18F-FDG-PET治疗。 BM ACT被定义为总骨髓(BM TOT)的子区域,其标准化摄取值(SUV)等于或高于该个体的平均值。非活动性骨髓(BM INACT)定义为BM TOT-BM ACT。广义线性建模用于测试BM ACT和BM INACT剂量量度与血液最低点之间的相关性,尤其是白细胞计数(WBC)和绝对中性粒细胞计数(ANC)。结果:增加的BM ACT平均剂量与log(WBC)最低点降低明显相关(β= -0.04; 95%CI,从-0.07到-0.01; p = 0.009),log(ANC)最低点降低(β= -0.05; 95%CI,-0.08至-0.02; p = 0.006),血红蛋白最低点降低(β= -0.16; 95%CI,-0.27至-0.05; p = 0.010),血小板最低点降低(β= -6.16; 95) %CI,-9.37至-2.96; p <0.001)。相比之下,BM INACT平均剂量与log(WBC)最低点之间没有关联(β= -0.01; 95%CI,-0.06至0.05; p = 0.84),log(ANC)最低点(β= -0.03; 95 %CI,-0.10至0.04; p = 0.40),血红蛋白最低点(β= -0.09; 95%CI,-0.31至0.14; p = 0.452),或血小板最低点(β= -3.47; 95%CI,-10.44)至3.50; p = 0.339)。结论:辐射具有较高18F-FDG-PET活性的BM区域与血液学毒性有关,支持以下假设:减少BM ACT区域的剂量可以减轻血液学毒性。未来的调查应设法确认这些发现并确定最佳SUV阈值以定义BM ACT。

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