TY - JOUR
T1 - Utility of comprehensive genomic profiling combined with machine learning for prognostic stratification in stage II/III colorectal cancer after adjuvant chemotherapy
AU - Kobayashi, Yosuke
AU - Suzuki, Yoshiyuki
AU - Seishima, Ryo
AU - Chikaishi, Yuko
AU - Matsuoka, Hiroshi
AU - Nakamura, Kohei
AU - Shigeta, Kohei
AU - Okabayashi, Koji
AU - Hiro, Junichiro
AU - Otsuka, Koki
AU - Uyama, Ichiro
AU - Saya, Hideyuki
AU - Nishihara, Hiroshi
AU - Suda, Koichi
AU - Kitagawa, Yuko
N1 - Publisher Copyright:
© The Author(s) under exclusive licence to Japan Society of Clinical Oncology 2025.
PY - 2025/5
Y1 - 2025/5
N2 - Background and purpose: Accurate recurrence risk evaluation in patients with stage II and III colorectal cancer (CRC) remains difficult. Traditional histopathological methods frequently fall short in predicting outcomes after adjuvant chemotherapy. This study aims to evaluate the use of comprehensive genomic profiling combined with machine learning for prognostic risk stratification in patients with CRC. Methods: A machine learning model was developed using a training cohort of 52 patients with stage II/III CRC who underwent curative surgery at Fujita Health University Hospital. Genomic DNA was isolated from formalin-fixed, paraffin-embedded tissue sections and analyzed with a 160 cancer-related gene panel. The random forest algorithm was used to determine key genes affecting recurrence-free survival. The model was validated by developing a risk score with internal and external cohorts, including 44 patients from Keio University Hospital. Results: Six key genes (KRAS, KIT, SMAD4, ARID2, NF1, and FBXW7) were determined as significant prognostic risk predictors. A risk score system integrating these genes with clinicopathological factors effectively stratified patients in both internal (p < 0.001) and external cohorts (p = 0.017). Conclusions: This study reveals that machine learning, combined with comprehensive genomic profiling, significantly improves prognostic risk stratification in patients with stage II/III CRC after adjuvant chemotherapy. This approach provides a promising tool for individualized treatment strategies, warranting further validation with larger cohorts.
AB - Background and purpose: Accurate recurrence risk evaluation in patients with stage II and III colorectal cancer (CRC) remains difficult. Traditional histopathological methods frequently fall short in predicting outcomes after adjuvant chemotherapy. This study aims to evaluate the use of comprehensive genomic profiling combined with machine learning for prognostic risk stratification in patients with CRC. Methods: A machine learning model was developed using a training cohort of 52 patients with stage II/III CRC who underwent curative surgery at Fujita Health University Hospital. Genomic DNA was isolated from formalin-fixed, paraffin-embedded tissue sections and analyzed with a 160 cancer-related gene panel. The random forest algorithm was used to determine key genes affecting recurrence-free survival. The model was validated by developing a risk score with internal and external cohorts, including 44 patients from Keio University Hospital. Results: Six key genes (KRAS, KIT, SMAD4, ARID2, NF1, and FBXW7) were determined as significant prognostic risk predictors. A risk score system integrating these genes with clinicopathological factors effectively stratified patients in both internal (p < 0.001) and external cohorts (p = 0.017). Conclusions: This study reveals that machine learning, combined with comprehensive genomic profiling, significantly improves prognostic risk stratification in patients with stage II/III CRC after adjuvant chemotherapy. This approach provides a promising tool for individualized treatment strategies, warranting further validation with larger cohorts.
KW - Colorectal neoplasms
KW - Genome testing
KW - Machine learning
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U2 - 10.1007/s10147-025-02722-4
DO - 10.1007/s10147-025-02722-4
M3 - Article
C2 - 40095334
AN - SCOPUS:105000246156
SN - 1341-9625
VL - 30
SP - 926
EP - 934
JO - International Journal of Clinical Oncology
JF - International Journal of Clinical Oncology
IS - 5
M1 - 103065
ER -