Urinary metabolomics may improve prediction of overall survival beyond tumor stage in colorectal cancer: results from the ColoCare study
BACKGROUND: Colorectal cancer (CRC) is a leading cause of cancer-related mortality. Prognosis is primarily guided by tumor stage despite substantial molecular heterogeneity. Urinary metabolomics may capture systemic and tumor-related biology beyond staging and could improve prognostic assessment. We hypothesized that incorporating urinary metabolomic profiles would improve overall survival (OS) prediction performance compared with a stage- and age-based reference model. METHOD: A total of n = 76 stage I-IV CRC patients recruited as part of the ColoCare Study in Heidelberg Germany with pre-surgery urinary metabolomics were included (23 deaths; median follow-up 3.03 years). Four metabolomics-based penalized Cox models adjusted for tumor stage and age at diagnosis were developed using LASSO, adaptive LASSO, spike-and-slab LASSO, and iterative sure independence screening (iSIS)-LASSO. Model discrimination was assessed using Harrell's C-index and time-dependent AUC based on the nested cross-validation. RESULTS: Compared with the reference model (Cox model including only tumor stage and age at diagnosis), all metabolomics-based models provided better discrimination. The spike-and-slab LASSO Cox model demonstrated the best performance, achieving a C-index of 0.75 (vs. 0.68) and consistently higher time-dependent AUCs at 1-5 years of follow-up, with a peak AUC of 0.76 at year 3 (vs. 0.68). Three urinary metabolites were consistently selected across all metabolomics-based models: indolelactate, 2-hydroxyisobutyrate and a uridine-like metabolite. CONCLUSIONS: Urinary metabolomics may improve CRC OS prediction beyond tumor stage and age at diagnosis, especially with the spike-and-slab LASSO Cox model. These results support urinary metabolomics as a promising noninvasive prognostic tool that merits external validation.
Authors
- Benjamin Haaland (ORCID: https://orcid.org/0000-0001-7263-0800)
- Boyi Guo (ORCID: https://orcid.org/0000-0003-2950-2349)
- David B. Liesenfeld
- Cornelia M. Ulrich (ORCID: https://orcid.org/0000-0001-7641-059X)
- Daniel O. Scharfstein (ORCID: https://orcid.org/0000-0001-7482-9653)
- Biljana Gigic (ORCID: https://orcid.org/0000-0002-8085-2072)
- Christoph Kahlert (ORCID: https://orcid.org/0000-0003-4124-7918)
- Erin M. Siegel (ORCID: https://orcid.org/0000-0003-1779-2510)
- Alexis Ulrich (ORCID: https://orcid.org/0000-0003-1469-2186)
- Tengda Lin (ORCID: https://orcid.org/0000-0001-5147-8432)
- Kenneth M. Boucher (ORCID: https://orcid.org/0000-0003-2833-0127)
- Jennifer Ose (ORCID: https://orcid.org/0000-0002-2030-9676)
- Paul A. Stewart
- Patricia A. Erickson
- Adetunji T. Toriola
- Victoria M. Bandera
- Victoria Damerell
- Sheetal Hardikar
- David Shibata
- Jane C. Figueiredo
- Doratha A. Byrd
- Christopher I. Li
- Jincheng Shen
Institutions
- Cedars-Sinai Medical Center (US)
- University of Tennessee Health Science Center (US)
- German Cancer Research Center (DE)
- Washington University in St. Louis (US)
- University of Utah (US)
- Heidelberg University (DE)
- Huntsman Cancer Institute (US)
- University Hospital Heidelberg (DE)
- Moffitt Cancer Center (US)
- Fred Hutch Cancer Center (US)
- National Center for Tumor Diseases (DE)
- Lukaskrankenhaus (DE)
- Hannover Re (Germany) (DE)
Publication Details
- Journal
- Metabolomics
- Published
- 2026-09-11
- DOI
- https://doi.org/10.1007/s11306-026-02516-3
- Primary Topic
- Metabolomics and Mass Spectrometry Studies
- Type
- article
- Field-Weighted Citation Impact
- 0.00