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On-treatment measurements of circulating tumor DNA during FOLFOX therapy in patients with colorectal cancer

机译:结直肠癌患者Folfox治疗过程中循环肿瘤DNA的处理测量

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摘要

a Schematic overview of the FOLFOX regimen and the time points of blood collection. All tumor tissues were analyzed for mutations in KRAS, and in some cases, BRAF and TP53 were sequenced as well. b Plasma DNA quantities of the patients and healthy controls (n = 60) (Student’s t-test; **p < 0.01, ***p < 0.001, ****p < 0.0001). All boxplots indicate the minimum and maximum value and median (center), and the interquartile range is shown by box and whiskers. c The median mutant allele frequencies (mAFs) for each plasma DNA analysis and the timing of each blood draw are displayed. Furthermore, the sum of longest diameters (SLD) as established by CT imaging for the selected target lesions according to RECIST are shown prior to (left side) and after (right side) completion of the FOLFOX cycle.
机译:Folfox方案的示意图和血液收集时间点。分析所有肿瘤组织在KRA中的突变中,并且在某些情况下,BRAF和TP53也被测序。 B血浆DNA数量的患者和健康对照(n = 60)(学生的t检验; ** p <0.01,*** p <0.001,**** p <0.0001)。所有Boxpots都表示最小值和最大值和中位数(中位数),并且框和晶须显示了额外的范围。 C显示每个血浆DNA分析的中位突变等位基因频率(MAF)和每个血液绘制的定时。此外,通过CT成像的最长直径(SLD)的总和根据再核,如recist在(左侧)和(右侧)完成Folfox循环之前。

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