LAUSR

Micro‐Abstract Mucinous colorectal cancer (CRC) is a unique histologic subtype that remains poorly defined. We aimed to better characterize this subtype of CRC and identified an increased frequency of mutations in GNAS, ERBB2, BRAF, KRAS, and SMAD4 with the mucinous histologic subtype, in addition to increased consensus molecular subtype (CMS) 1 (microsatellite instability immune) and decreased CMS2 (canonical) prevalence. Adverse clinical features included microsatellite instability and synchronous metastatic disease at presentation. Even after controlling for clinical and mutation differences, the mucinous histologic subtype was associated with worse overall survival. Background The mucinous histologic subtype accounts for 5% to 20% of colorectal cancer (CRC) cases but remains poorly characterized. The present study characterized the baseline characteristics, mutational profile, and clinical outcomes of patients diagnosed with mucinous CRC. Materials and Methods We identified 1877 patients with metastatic CRC with available histologic findings and molecular profiling and summarized the baseline clinical and pathologic characteristics and overall survival (OS) stratified by the histologic type. The data from separate cohorts with consensus molecular subtype (CMS) and CpG island methylator information were also summarized. Results The mucinous histologic type was found in 277 of the 1877 patients (14.8%) and was associated with an increased prevalence of microsatellite instability (P < .001) and a right‐sided primary (P < .001). An increased frequency of CMS1 (microsatellite instability immune) and lower rates of CMS2 (canonical) were identified, with mucinous compared with nonmucinous adenocarcinoma (P < .0001). Mutations in SMAD4 (P < .001), GNAS (P < .001), ERBB2 (P = .02), BRAF (P < .001), and KRAS (P < .001) occurred at greater frequencies in the mucinous CRC cases, and TP53 (P < .001), APC (P < .001), and NRAS mutations (P = .03) were less common. Univariate (hazard ratio [HR], 1.38; 95% confidence interval [CI], 1.17‐1.63; P < .001) and multivariate analysis (HR, 1.36; 95% CI, 1.12‐1.64; P = .002) demonstrated that the mucinous histologic type is associated with worse OS. The features associated with the mucinous histologic subtype were independent predictors for shorter OS, including BRAF (HR, 1.74; 95% CI, 1.35‐2.25; P < .001) and KRAS (HR, 1.42; 95% CI, 1.22‐1.65; P < .001) mutations, right‐sided location (HR, 1.20; 95% CI, 1.04‐1.39; P = .01), and synchronous metastases (HR, 2.92; 95% CI, 2.49‐3.42; P < .001). Conclusion Compared with nonmucinous adenocarcinoma, the mucinous histologic type is associated with a worse prognosis, even when controlling for known prognostic features. This unique biologic behavior should be considered in the treatment and prognostic assessment of patients with CRC.