EXPLAINING TRANSITION FROM STAGE II TO STAGES III AND IV COLON CANCER THROUGH ASSESSMENT OF TUMOR MICROENVIRONMENT AND ACTIONABLE SOMATIC MUTATIONS
Responsible supervisor of the SVOČ project: Andriy Trailin, MD, DSc, andriy.trailin@lfp.cuni.cz
Brief description of the Student´s scientific activity project:
More than half of new colon cancer (CC) patients in the Czech Republic presented at diagnosis with metastases in regional lymph nodes (RLNs) (stage III) and distant metastases (stage IV). Survival in CC is successively worse in stages III and IV compared with stage II. Treatment of stage II CC consists of surgical resection and then adjuvant therapy is used in patients with a high risk of recurrence. The identification of stage II CC patients in a high risk of developing RLNs or distant metastasis through the use of additional morphological and molecular risk factors is important to support clinical decision making on the follow-up and use of adjuvant therapy.
Our hypothesis posits that histopathological changes in the primary tumor and RLNs along with immune tumor microenvironment (TME) and cancer genomics will reveal specific pathways underlying the metastatic process.
We also hypothesize that the extent and characteristics of angiogenesis in the primary carcinoma-RLNs axis is a prerequisite for the metastatic spread.
We further posit that differences in the mutational patterns between primary tumor, RLNs and distant metastases may explain distinct metastatic potential of individual tumors.
We assume that the results of our study could bring new insights to the understanding of CC metastatic process and especially we could define a high-risk profile predictive of early metastasis leading to personalized selection of stage II CC patients suitable for adjuvant chemotherapy and active follow-up. A fundamentally novel tumor biological assessment of primary tumor and RLNs from the same patients will provide important data on the role of various players in the TME on patient outcome. Integrative analyses of the TME at the various steps of the metastatic cascade should highlight their relative contribution to the metastatic spread and to delineate the role of tumor and immune parameters to this process.
Students will be primarily engaged into image analysis using QuPath software.
2 students, optimal frequency is 2 times per week, however, remote work is possible.
Results will be presented on students’ scientific conference. Considering the extent and quality of scientific contribution students might be acknowledged in the paper or become co-authors.