Background
Although serum tumour markers (STMs), clinicopathological characteristics and the status of KRAS and MMR play an important role in optimizing the treatment and improving the prognosis of colorectal cancer, their interrelationships remain largely unknown.
Methods
A retrospective analysis of 2279 patients who underwent KRAS or MMR status testing and STM measurements prior to treatment over the past four years was conducted. Univariate and multivariate logistic regression were performed to identify independent predictive factors of KRAS and MMR status. The area under receiver operating characteristic (ROC) curve (AUC) was used to evaluate the predictive value of individual and combined factors.
Results
Of the 784 patients tested for KRAS and 2279 patients tested for MMR status, KRAS mutations and dMMR were identified in 276 patients (35.20%) and 177 patients (7.77%), respectively. Logistic regression analysis demonstrated that right colon, well and moderate differentiation and negative CA19-9 were independent predictors for KRAS mutations. The ROC curve yielded an AUC of 0.609 for the combination of the three factors. Age < 65 was an independent predictive factor for dMMR, along with tumour size > 4.6 cm, right colon, poor differentiation, harvested lymph nodes ≥ 22, no lymph node metastasis, no perineural invasion, negative CEA and positive CA72-4. When the nine criteria were used together, the AUC was 0.849.
Conclusion
Both STMs and clinicopathological characteristics were found to be significantly associated with the status of KRAS and MMR. The combination of these two factors possessed a strong predictive power for targeted genes among CRC patients.