Survival of metastatic colorectal cancer (mCRC) patients has improved, but mainly for trial patients. New predictive and prognostic biomarkers validated in the general mCRC population are needed. Caudal-type homeobox 2 (CDX2) is an intestine-specific transcription factor with potential prognostic and predictive effect, but the importance in mCRC has not been fully investigated. Immunohistochemistry analysis of CDX2 was performed in a Scandinavian population-based cohort of mCRC ( = 796). Frequency, clinical and tumor characteristics, response rate, progression-free survival, and overall survival (OS) were estimated. Loss of CDX2 expression was found in 87 (19%) of 452 stained cases, in 53% if mutated (mut) and in 9% if mutated (mut). CDX2 loss was associated with microsatellite instability, mut, and poor differentiation and inversely associated with mut. Patients with CDX2 loss received less first-line (53 vs. 64%, = 0.050) and second-line (23 vs. 39%, = 0.006) chemotherapy and secondary surgery (1 vs. 9%, = 0.019). Median progression-free survival and OS for patients given first-line combination chemotherapy was 4 and 10 months if CDX2 loss vs. 9 and 24 months if CDX2 expressed ( = 0.001, < 0.001). Immediate progression on first-line combination chemotherapy was seen in 35% of patients with CDX2 loss vs. 10% if CDX2 expressed ( = 0.003). Median OS in patients with mut or mut and CDX2 expressed in tumor (both 21 months) was comparable to wild-type patients (27 months). However, if CDX2 loss, median OS was only 8 and 11 months in mut and mut cases, respectively, and 10 months in double wild-type patients. In multivariate analysis, CDX2 loss (hazard ratio: 1.50, = 0.027) and mut (hazard ratio: 1.62, = 0.012) were independent poor prognostic markers for OS. In a population-based cohort of mCRC patients, CDX2 loss is an independent poor prognostic marker. Expression of CDX2 defines a new subgroup of mut cases with a much better prognosis. Loss of CDX2 defines a small group of mut cases with a worse prognosis. Patients with CDX2 loss receive less palliative chemotherapy with less benefit and rarely reach secondary surgery.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7026487PMC
http://dx.doi.org/10.3389/fonc.2020.00008DOI Listing

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