Sex Differences and Tumor Blood Flow from Dynamic Susceptibility Contrast MRI Are Associated with Treatment Response after Chemoradiation and Long-term Survival in Rectal Cancer.

Radiology

From the Department of Oncology, Akershus University Hospital, Epigen, Akershus Universitetssykehus HF, 1478 Lørenskog, Norway (K.M.B., S.M., K.I.G., A.H.R., K.R.R.); Department of Physics (K.M.B., A.B.) and Institute of Clinical Medicine (A.N., A.H.R.), University of Oslo, Oslo, Norway; Department of Diagnostic Physics, Division of Radiology and Nuclear Medicine, Oslo University Hospital, Oslo, Norway (E.G., A.B.); Department of Optometry, Radiography and Lighting Design, University of South-Eastern Norway, Drammen, Norway (E.G.); Department of Radiology, Akershus University Hospital, Lørenskog, Norway (A.N., S.H.H.); Sunnmøre MR-Klinikk, Ålesund, Norway (K.I.G.); and Department of Physics, Norwegian University of Science and Technology, Trondheim, Norway (K.R.R.).

Published: November 2020

Background MRI is the standard tool for rectal cancer staging. However, more precise diagnostic tests that can assess biologic tumor features decisive for treatment outcome are necessary. Tumor perfusion and hypoxia are two important features; however, no reference methods that measure these exist in clinical use. Purpose To assess the potential predictive and prognostic value of MRI-assessed rectal cancer perfusion, as a surrogate measure of hypoxia, for local treatment response and survival. Materials and Methods In this prospective observational cohort study, 94 study participants were enrolled from October 2013 to December 2017 (ClinicalTrials.gov: NCT01816607). Participants had histologically confirmed rectal cancer and underwent routine diagnostic MRI, an extended diffusion-weighted sequence, and a multiecho dynamic contrast agent-based sequence. Predictive and prognostic values of dynamic contrast-enhanced, dynamic susceptibility contrast (DSC), and intravoxel incoherent motion MRI were investigated with response to neoadjuvant treatment, progression-free survival, and overall survival as end points. Secondary objectives investigated potential sex differences in MRI parameters and relationship with lymph node stage. Statistical methods used were Cox regression, Student test, and Mann-Whitney test. Results A total of 94 study participants (mean age, 64 years ± 11 [standard deviation]; 61 men) were evaluated. Baseline tumor blood flow from DSC MRI was lower in patients who had poor local tumor response to neoadjuvant treatment (96 mL/min/100 g ± 33 for ypT2-4, 120 mL/min/100 g ± 21 for ypT0-1; = .01), shorter progression-free survival (hazard ratio = 0.97; 95% confidence interval: 0.96, 0.98; < .001), and shorter overall survival (hazard ratio = 0.98; 95% confidence interval: 0.98, 0.99; < .001). Women had higher blood flow (125 mL/min/100 g ± 27) than men (74 mL/min/100 g ± 26, < .001) at stage 4. Volume transfer constant and plasma volume from dynamic contrast-enhanced MRI as well as Δ* peak and area under the curve for 30 and 60 seconds from DSC MRI were associated with local malignant lymph nodes (pN status). Median area under the curve for 30 seconds was 0.09 arbitrary units (au) ± 0.03 for pN1-2 and 0.19 au ± 0.12 for pN0 ( = .001). Conclusion Low tumor blood flow from dynamic susceptibility contrast MRI was associated with poor treatment response in study participants with rectal cancer. © RSNA, 2020

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http://dx.doi.org/10.1148/radiol.2020200287DOI Listing

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