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. 2022 May 2;6(3):zrac033.
doi: 10.1093/bjsopen/zrac033.

MRI tumour regression grade in locally recurrent rectal cancer

Affiliations

MRI tumour regression grade in locally recurrent rectal cancer

Eva L K Voogt et al. BJS Open. .

Abstract

Background: This study aimed to investigate the agreement between magnetic resonance tumour regression grade (mrTRG) and pathological regression grade (pTRG) in patients with locally recurrent rectal cancer (LRRC). Also, the reproducibility of mrTRG was investigated.

Methods: All patients with LRRC who underwent a resection between 2010 and 2018 after treatment with induction chemotherapy and neoadjuvant chemo(re)irradiation in whom a restaging MRI was available were retrospectively selected. All MRI scans were reassessed by two independent radiologists using the mrTRG, and the pTRG was reassessed by an independent pathologist. The interobserver agreement between the radiologists as well as between the radiologists and the pathologist was assessed with the weighted kappa test. A subanalysis was performed to evaluate the influence of the interval between imaging and surgery.

Results: Out of 313 patients with LRRC treated during the study interval, 124 patients were selected. Interobserver agreement between the radiologists was fair (k = 0.28) using a two-tier grading system (mrTRG 1-2 versus mrTRG 3-5). For the lead radiologist, agreement with pTRG was moderate (k = 0.52; 95 per cent c.i. 0.36 to 0.68) when comparing good (mrTRG 1-2 and Mandard 1-2) and intermediate/poor responders (mrTRG 3-5 and Mandard 3-5), and the agreement was fair between the other abdominal radiologist and pTRG (k = 0.39; 95 per cent c.i. 0.22 to 0.56). A shorter interval (less than 7 weeks) between MRI and surgery resulted in an improved agreement (k = 0.69), compared with an interval more than 7 weeks (k = 0.340). For the lead radiologist, the positive predictive value for predicting good responders was 95 per cent (95 per cent c.i. 71 per cent to 99 per cent), whereas this was 56 per cent (95 per cent c.i. 44 per cent to 66 per cent) for the other radiologist.

Conclusion: This study showed that, in LRRC, the reproducibility of mrTRG among radiologists is limited and the agreement of mrTRG with pTRG is low. However, a shorter interval between MRI and surgery seems to improve this agreement and, if assessed by a dedicated radiologist, mrTRG could predict good responders.

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Figures

Fig. 1
Fig. 1
Flowchart showing patient selection
Fig. 2
Fig. 2
MRI at baseline and after chemoradiotherapy showing a complete radiological response (mrTRG 1) and the corresponding histology imaging showing a complete response (pTRG 1). In this case, restaging was performed at less than 7 weeks. mrTRG, magnetic resonance tumour regression grade; pTRG, pathologic regression grade.
Fig. 3
Fig. 3
MRI at baseline and after chemoradiotherapy showing a near complete radiological response (mrTRG 2). In this case, restaging was performed at less than 7 weeks. mrTRG, magnetic resonance tumour regression grade.
Fig. 4
Fig. 4
MRI at baseline and after chemoradiotherapy showing a moderate radiological response (mrTRG 3). In this case, restaging was performed at more than 7 weeks. mrTRG, magnetic resonance tumour regression grade.
Fig. 5
Fig. 5
MRI at baseline and after chemoradiotherapy showing a slight radiological response (mrTRG 4). In this case, restaging was performed at more than 7 weeks. mrTRG, magnetic resonance tumour regression grade.
Fig. 6.
Fig. 6.
MRI at baseline and after chemoradiotherapy showing no radiological response (mrTRG 5) and the corresponding histology imaging showing no regressive changes (pTRG 5). In this case, restaging was performed at less than 7 weeks. mrTRG, magnetic resonance tumour regression grade; pTRG, pathologic regression grade.

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