Purpose <p>To determine whether the apparent diffusion coefficient (ADC) parameters of tumor and distal paracancerous tissues in rectal adenocarcinoma (RA) derived from diffusion weighted imaging (DWI) can be associated with the tumor stages.</p> Materials and methods <p>134 consecutive patients with RA underwent preoperative DWI. ADC values of the tumor, distal tumor-adjacent and tumor-distant tissues were measured (recorded as ADC<sub>t</sub>, ADC<sub>dta</sub> and ADC<sub>dtd</sub>, respectively). Additionally, ratios of ADC<sub>t</sub> to ADC<sub>dta</sub> (ADC<sub>t/dta</sub>), ADC<sub>t</sub> to ADC<sub>dtd</sub> (ADC<sub>t/dtd</sub>), and ADC<sub>dta</sub> to ADC<sub>dtd</sub> (ADC<sub>dta/dtd</sub>) were calculated. Student’s t-test or Mann–Whitney U test, with false discovery rate (FDR) correction, was performed to compare the differences in the aforementioned ADC parameters between different tumor stages. The diagnostic efficacy of individual ADC and combined ADC parameters was evaluated using logistic regression analysis and receiver operating characteristic (ROC) analysis to predict tumor stages.</p> Results <p>Tumors with pT<sub>3–4</sub> stage demonstrated significantly lower values of ADC<sub>t</sub>, ADC<sub>t/dta</sub>, and ADC<sub>t/dtd</sub> compared to those with pT<sub>1–2</sub> stage; tumors with pN<sub>1–2</sub> stage exhibited significantly lower values of ADC<sub>t</sub> and ADC<sub>t/dta</sub> compared to those with pN<sub>0</sub> stage; and cases with lymph node metastasis (LNM) showed significantly lower values of ADC<sub>t</sub>, ADC<sub>t/dta</sub>, and ADC<sub>t/dtd</sub> compared to those without LNM (all FDR- corrected <i>P</i>-values &lt; 0.10). Area under the ROC curves (AUC) of the combination involving ADC<sub>t</sub> and ADC<sub>t/dta</sub> was higher than that of individual ADC parameters when assessing pT stage, pN stage, and LNM.</p> Conclusion <p>The ADC parameters of tumor and distal paracancerous tissues may provide supplementary information for preoperatively assessing tumor stages in RA.</p>

错误:搜索内容不能为空,请输入英文关键词
错误:关键词超出字数限制,请精简
高级检索

Apparent diffusion coefficients of resectable rectal adenocarcinoma and distal paracancerous tissues derived from diffusion weighted imaging: association with tumor stage

  • Hui Luo,
  • Yue-qin Gou,
  • Yue-su Wang,
  • Hui-lin Qin,
  • Hai-ying Zhou,
  • Xiao-ming Zhang,
  • Tian-wu Chen

摘要

Purpose

To determine whether the apparent diffusion coefficient (ADC) parameters of tumor and distal paracancerous tissues in rectal adenocarcinoma (RA) derived from diffusion weighted imaging (DWI) can be associated with the tumor stages.

Materials and methods

134 consecutive patients with RA underwent preoperative DWI. ADC values of the tumor, distal tumor-adjacent and tumor-distant tissues were measured (recorded as ADCt, ADCdta and ADCdtd, respectively). Additionally, ratios of ADCt to ADCdta (ADCt/dta), ADCt to ADCdtd (ADCt/dtd), and ADCdta to ADCdtd (ADCdta/dtd) were calculated. Student’s t-test or Mann–Whitney U test, with false discovery rate (FDR) correction, was performed to compare the differences in the aforementioned ADC parameters between different tumor stages. The diagnostic efficacy of individual ADC and combined ADC parameters was evaluated using logistic regression analysis and receiver operating characteristic (ROC) analysis to predict tumor stages.

Results

Tumors with pT3–4 stage demonstrated significantly lower values of ADCt, ADCt/dta, and ADCt/dtd compared to those with pT1–2 stage; tumors with pN1–2 stage exhibited significantly lower values of ADCt and ADCt/dta compared to those with pN0 stage; and cases with lymph node metastasis (LNM) showed significantly lower values of ADCt, ADCt/dta, and ADCt/dtd compared to those without LNM (all FDR- corrected P-values < 0.10). Area under the ROC curves (AUC) of the combination involving ADCt and ADCt/dta was higher than that of individual ADC parameters when assessing pT stage, pN stage, and LNM.

Conclusion

The ADC parameters of tumor and distal paracancerous tissues may provide supplementary information for preoperatively assessing tumor stages in RA.