ArticleBJR open2026
Optimal time for MRI response evaluation in squamous cell carcinoma of the anus.
Article in BJR open, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01937780 (Anal Cancer Radiotherapy - Prospective Study of Treatment Outcome, Patient-Reported Outcomes, Utility of Imaging and Biomarkers, and Cancer Survivorship), which is not on this map. Not yet cited in PubMed.
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Anal Cancer Radiotherapy - Prospective Study of Treatment Outcome, Patient-Reported Outcomes, Utility of Imaging and Biomarkers, and Cancer Survivorship
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8 authors.
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Abstract
Objectives: To identify the optimal time for MRI response evaluation after chemoradiotherapy (CRT) in squamous cell carcinoma of the anus (SCCA) and to employ combined T2+diffusion-weighted MRI tumour regression grade (comrTRG). Methods: We assessed the positive and negative predictive values (PPV, NPV) of post-treatment MRI in a retrospective mono-centre diagnostic accuracy study that prospectively included consecutive patients treated between 2013 and 2017. Index tests were MRI at 6-, 12-, and 24-weeks post-treatment (6w, 12w, and 24w) to detect locoregional treatment failures (LRTF). Clinical outcome served as reference standard. Tumour regression was assessed using comrTRG based on radiological reports. Mixed-effects logistic regression was used to compare the comrTRG score across time points. The analyses were stratified by patients' T/N stage and human papillomavirus (HPV) status. Results: For 127 included patients (62 years ± 11 [mean ± SD]; 92 women), 261 post-treatment MRI reports (6w: Conclusions: MRI performed more reliably after 24 weeks. Timely assessment may aid early LRTF detection. Tailoring follow-up with frequent MRI scans may be sufficient for high-risk patients. Combined mrTRG is practical for describing response in SCCA. Advances in knowledge: Post-treatment MRI assessment at later time points is preferable in SCCA to avoid inconclusive imaging and unnecessary salvage surgery. The introduced comrTRG is a practical tool for response evaluation. Registration: ClinicalTrials.gov: NCT01937780.
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