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收稿:2016-12-12,
纸质出版:2017-05-15
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张丹, 陈康, 谯智慧, 等. 表观弥散系数与非小细胞肺癌预后分子生物学指标的相关性分析[J]. 第三军医大学学报, 2017,39(9):913-918.
Dan Zhang, Kang Chen, Zhihui Qiao, et al. Correlation of apparent diffusion coefficient with common prognostic molecular biological indicators of non-small cell lung cancer[J]. Journal of Third Military Medical University, 2017, 39(9): 913-918.
张丹, 陈康, 谯智慧, 等. 表观弥散系数与非小细胞肺癌预后分子生物学指标的相关性分析[J]. 第三军医大学学报, 2017,39(9):913-918. DOI: 10.16016/j.1000-5404.201612077.
Dan Zhang, Kang Chen, Zhihui Qiao, et al. Correlation of apparent diffusion coefficient with common prognostic molecular biological indicators of non-small cell lung cancer[J]. Journal of Third Military Medical University, 2017, 39(9): 913-918. DOI: 10.16016/j.1000-5404.201612077.
Objective
2
To analyze the correlation of apparent diffusion coefficient (ADC) with common prognostic molecular biological indicators of non-small cell lung cancer (NSCLC).
Methods
2
Thirty-nin
e patients with histopathologically conformed NSCLC admitted in the Department of Respiratory Diseases from April 2015 to September 2016 were recruited in this study. All the patients underwent diffusion weighted imaging (DWI)
ADCs were calculated based on DW images. Students'
t
test and single factor analysis of variance were applied to analyze the differences of ADCs in biological indicators
serum cancer embryo antigen (CEA)
positive rate of Ki67
thyroid transcription factor 1 (TTF-1)
and epidermal growth factor receptor (EGFR). Spearman rank correlation was used to analyze the correlations of the ADCs with above indicators.
Results
2
The ADCs in different indicators
such as CEA
Ki67
TTF-1 and EGFR were significantly different (
P
<
0.01). Negative correlations were found between ADCs and above biological indicators (CEA:
r
=-0.77
P
<
0.001; Ki67:
r
=-0.58
P
<
0.001; TTF-1:
r
=-0.47
P
=0.003; EGFR:
r
=-0.40
P
=0.012).
Conclusion
2
ADCs are negatively correlated with common prognostic indicators CEA
Ki67
TTF-1 and EGFR. Lower ADCs commonly suggest higher CEA and Ki67
which might predict positive TTF-1 and EGFR mutations.
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