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[Diffusion-weighted MR imaging in patients with rectal cancer: our initial experience]
Alberto Seehaus1, Carlos Vacaro, Jorge Ocantos
1Servicio de Diagnóstico por Imágenes, Hospital Italiano de Buenos Aires, Ciudad Autónoma de Buenos Aires, Argentina. alberto.seehaus@hospitalitaliano.org.ar
Diffusion MRI effectively identifies residual rectal cancer after neoadjuvant therapy. Quantitative apparent diffusion coefficient (ADC) measurements improve detection of complete pathologic response (CPR) and residual primary tumor (RPT).
Area of Science:
- Oncology
- Radiology
- Medical Imaging
Background:
- Accurate pre-surgical characterization of post-neoadjuvant residual tumor response in rectal cancer is crucial for treatment planning.
- Imaging techniques can guide therapeutic strategies or observation decisions in rectal cancer patients.
Purpose of the Study:
- To evaluate the role of diffusion-weighted magnetic resonance imaging (DWMR) in determining residual primary tumor (RPT) or complete pathologic response (CPR) after neoadjuvant therapy in rectal cancer (RC).
- To compare the diagnostic performance of visual and quantitative DWMR assessments against pathological anatomy as the gold standard.
Main Methods:
- Eighteen rectal cancer patients with medial/low tumors and positive lymph nodes underwent neoadjuvant treatment.
- Post-neoadjuvant DWMR was performed using visual and quantitative scales to measure apparent diffusion coefficient (ADC).
- Results were correlated with pathological anatomy findings.
Main Results:
- Pathological anatomy revealed RPT in 15 of 18 patients and CPR in 3.
- Visual DWMR detected RPT in 14/15 patients; quantitative ADC detected all RPT cases.
- Quantitative ADC detected all 3 CPR cases, while visual DWMR detected 2/3.
Conclusions:
- DWMR is a valuable tool for assessing post-neoadjuvant RPT and CPR in rectal cancer.
- Quantitative ADC assessment significantly enhances diagnostic accuracy compared to qualitative visual analysis.
- DWMR, particularly with quantitative ADC, improves the determination of treatment response in rectal cancer.
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