Magnetic Resonance Imaging–Detected Tumor Response for Locally Advanced Rectal Cancer Predicts Survival Outcomes: MERCURY Experience

Author:

Patel Uday B.1,Taylor Fiona1,Blomqvist Lennart1,George Christopher1,Evans Hywel1,Tekkis Paris1,Quirke Philip1,Sebag-Montefiore David1,Moran Brendan1,Heald Richard1,Guthrie Ashley1,Bees Nicola1,Swift Ian1,Pennert Kjell1,Brown Gina1

Affiliation:

1. Uday B. Patel, Paris Tekkis, Kjell Pennert, Gina Brown, Royal Marsden Hospital, Chelsea and Sutton; Fiona Taylor, Nicola Bees, Ian Swift, Mayday University Hospital, Croydon; Christopher George, Epsom General Hospital, Epsom; Hywel Evans, Frimley Park Hospital, Frimley; Phillip Quirke, Leeds Institute of Molecular Medicine, University of Leeds; David Sebag-Monegiore, Ashley Guthrie, St James Institute of Oncology, Leeds; Brendan Moran, Richard Heald, Pelican Cancer Foundation, North Hampshire Hospital,...

Abstract

Purpose To assess magnetic resonance imaging (MRI) and pathologic staging after neoadjuvant therapy for rectal cancer in a prospectively enrolled, multicenter study. Methods In a prospective cohort study, 111 patients who had rectal cancer treated by neoadjuvant therapy were assessed for response by MRI and pathology staging by T, N and circumferential resection margin (CRM) status. Tumor regression grade (TRG) was also assessed by MRI. Overall survival (OS) was estimated by using the Kaplan-Meier product-limit method, and Cox proportional hazards models were used to determine associations between staging of good and poor responders on MRI or pathology and survival outcomes after controlling for patient characteristics. Results On multivariate analysis, the MRI-assessed TRG (mrTRG) hazard ratios (HRs) were independently significant for survival (HR, 4.40; 95% CI, 1.65 to 11.7) and disease-free survival (DFS; HR, 3.28; 95% CI, 1.22 to 8.80). Five-year survival for poor mrTRG was 27% versus 72% (P = .001), and DFS for poor mrTRG was 31% versus 64% (P = .007). Preoperative MRI-predicted CRM independently predicted local recurrence (LR; HR, 4.25; 95% CI, 1.45 to 12.51). Five-year survival for poor post-treatment pathologic T stage (ypT) was 39% versus 76% (P = .001); DFS for the same was 38% versus 84% (P = .001); and LR for the same was 27% versus 6% (P = .018). The 5-year survival for involved pCRM was 30% versus 59% (P = .001); DFS, 28 versus 62% (P = .02); and LR, 56% versus 10% (P = .001). Pathology node status did not predict outcomes. Conclusion MRI assessment of TRG and CRM are imaging markers that predict survival outcomes for good and poor responders and provide an opportunity for the multidisciplinary team to offer additional treatment options before planning definitive surgery. Postoperative histopathology assessment of ypT and CRM but not post-treatment N status were important postsurgical predictors of outcome.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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