A Mathematical Model for Assessing KRAS Mutation Effect on Monoclonal Antibody Treatment of Colorectal Cancer

The most challenging task in colorectal cancer research nowadays is to understand the development of acquired resistance to antiEGFR drugs. The key reason for this problem is the KRAS mutations produced after the treatment with monoclonal antibodies (mAb). KRAS screening tests done before the start of the treatment are not very sensitive to identify minute quantity of the mutated cells, which can produce resistance to the therapy after the beginning of the treatment. Here we present a mathematical model for the analysis of KRAS mutations behavior in colorectal cancer with respect to mAb treatments. To evaluate the drug performance we have developed equations for two types of tumors cells, i.e KRAS mutated and KRAS wildtype. Both tumor cell populations were treated with a combination of mAb and chemotherapy drugs. It was observed that even the minimal initial concentration of KRAS mutation before the treatment has the ability to make the tumor refractory to the treatment. Patient's immune responses are speci cally taken into considerations and it is found that, in case of KRAS mutations, the immune strength has no e ect on medication e cacy. Finally, Cetuximab (mAb) and Irinotecan (chemotherapy) drugs are analyzed as rst-line treatment of colorectal cancer with few KRAS mutated cells. Results show that this is only e ective for patients with high immune strength and it should not be recommended as rst-line therapy for patients with moderate and weak immune systems because of potential risk of relapse, with KRAS mutant cells acquired resistance involved with them.