Diffusion-weighted imaging: Apparent diffusion coefficient histogram analysis for detecting pathologic complete
Moon Hyung Choi1, Soon Nam Oh1, Sung Eun Rha1
1Department of Radiology, Seoul St. Mary's Hospital, Catholic University of Korea, Seoul, Republic of Korea.
Journal of Magnetic Resonance Imaging : JMRI
|December 16, 2015
Summary
Apparent diffusion coefficient (ADC) histogram analysis on MRI can predict pathologic complete response (pCR) after rectal cancer chemoradiotherapy. Lower ADC values in rectal tumors indicate a higher likelihood of pCR.
Area of Science:
- Radiology
- Oncology
- Medical Imaging
Background:
- Neoadjuvant chemoradiotherapy (CRT) is standard for rectal cancer.
- Evaluating treatment response, specifically pathologic complete response (pCR), is crucial for patient management.
- Preoperative magnetic resonance imaging (MRI) is used to assess tumor stage and response.
Purpose of the Study:
- To assess the utility of apparent diffusion coefficient (ADC) values from histogram analysis of whole rectal tumors.
- To determine if ADC histogram parameters can quantitatively evaluate pCR after neoadjuvant CRT using preoperative MRI.
Main Methods:
- 86 rectal cancer patients undergoing surgery post-neoadjuvant CRT were analyzed.
- Two blinded radiologists performed quantitative image analysis using T2-weighted and diffusion-weighted MRI.
- Dedicated software generated ADC histograms to assess whole tumor ADC distribution.
Main Results:
- 18.6% of patients achieved pCR.
- ADC histogram parameters showed excellent inter-reader agreement.
- Post-CRT ADC histogram values (minimum, 10th, 25th, 50th, 75th percentiles, and mean) were significantly higher in the pCR group.
- The 25th percentile of post-CRT ADC demonstrated the best diagnostic performance for pCR (AUC=0.796).
Conclusions:
- Low percentile ADC values from histogram analysis of rectal cancer on post-CRT MRI significantly differentiate between pCR and non-pCR groups.
- ADC histogram analysis provides a quantitative and objective marker for evaluating complete pathologic response to preoperative CRT in rectal cancer.
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