A clinical decision support system optimising adjuvant chemotherapy for colorectal cancers by integrating deep learning and pathological staging markers: a development and validation study

The DoMore-v1-CRC marker was recently developed using deep learning and conventional haematoxylin and eosin-stained tissue sections, and was observed to outperform established molecular and morphological markers of patient outcome after primary colorectal cancer resection. The aim of the present stu...

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Veröffentlicht in:The lancet oncology 2022-09, Vol.23 (9), p.1221-1232
Hauptverfasser: Kleppe, Andreas, Skrede, Ole-Johan, De Raedt, Sepp, Hveem, Tarjei S, Askautrud, Hanne A, Jacobsen, Jørn E, Church, David N, Nesbakken, Arild, Shepherd, Neil A, Novelli, Marco, Kerr, Rachel, Liestøl, Knut, Kerr, David J, Danielsen, Håvard E
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Sprache:eng
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Zusammenfassung:The DoMore-v1-CRC marker was recently developed using deep learning and conventional haematoxylin and eosin-stained tissue sections, and was observed to outperform established molecular and morphological markers of patient outcome after primary colorectal cancer resection. The aim of the present study was to develop a clinical decision support system based on DoMore-v1-CRC and pathological staging markers to facilitate individualised selection of adjuvant treatment. We estimated cancer-specific survival in subgroups formed by pathological tumour stage (pT12) if not pN2, and DoMore-v1-CRC classification (good, uncertain, or poor prognosis) in 997 patients with stage II or III colorectal cancer considered to have no residual tumour (R0) from two community-based cohorts in Norway and the UK, and used these data to define three risk groups. An external cohort of 1075 patients with stage II or III R0 colorectal cancer from the QUASAR 2 trial was used for validation; these patients were treated with single-agent capecitabine. The proposed risk stratification system was evaluated using Cox regression analysis. We similarly evaluated a risk stratification system intended to reflect current guidelines and clinical practice. The primary outcome was cancer-specific survival. The new risk stratification system provided a hazard ratio of 10·71 (95% CI 6·39–17·93; p
ISSN:1470-2045
1474-5488
DOI:10.1016/S1470-2045(22)00391-6