Published online Jan 14, 2024. doi: 10.3748/wjg.v30.i2.158
Peer-review started: October 25, 2023
First decision: November 12, 2023
Revised: November 23, 2023
Accepted: December 14, 2023
Article in press: December 14, 2023
Published online: January 14, 2024
Processing time: 78 Days and 15.4 Hours
Tumor budding (TB) is a novel prognostic biomarker that may influence clinical treatment decisions in stage I-II colorectal cancer (CRC) patients. This study analyzed the relationship between TB categories and clinicopathological characteristics and assess their prognostic value in stage III-IV CRC to further refine the prognostic risk stratification of stage III-IV CRC. Additionally, we analyzed changes in tumor-infiltrating lymphocytes (TILs) in patients with different TB categories and initially explored the correlation between TB and the tumor immune microenvironment.
To explore the association of TB with clinicopathological features and prognostic value in stage III-IV CRC.
This study analyzed the relationship between TB categories and clinicopathological characteristics and assess their prognostic value in stage III-IV CRC to further refine the prognostic risk stratification of stage III-IV CRC.
This study included a substantial number of 547 CRC patients. TB was evaluated independently by two pathologists and re-evaluated by a third pathologist when the results were inconsistent, ensuring a high level of reliability in the TB assessment. Furthermore, the 2016 International TB Consensus Conference recommendations were followed to evaluate TB specifically in patients with stage III-IV CRC, thereby investigating its impact on patient prognosis.
Multivariate Cox proportional hazards regression analysis demonstrated that chemotherapy, clinical stage IV, ≥ 4 regional lymph node metastases, left-sided colonic cancer, and Bd 2-3 were independent prognostic factors in patients with stage III-IV CRC. Moreover, the density of TILs was higher in Bd 1 than in Bd 2-3, both in the tumor stroma and its invasive margin.
TB has an independent predictive prognostic value for progression-free survival and overall survival in patients with stage III-IV CRC. It is recommended to complete the TB report of stage III-IV CRC cases in the standardized pathological report to further refine risk stratification.
A multicenter prospective study with large samples should be conducted in the future, and constructing a prognosis model with a multi-index multidimensional association algorithm with other prediction models is needed to further verify its reliability.