Targeting Tumor Microenvironment Modulation for Improved Outcomes in Immunotherapy-Based Cancer Treatments
Main Article Content
Abstract
Background: Immunotherapy has revolutionized cancer treatment, yet its efficacy is often limited by the hostile tumor microenvironment (TME), which hampers immune responses and promotes tumor growth. Objective: This study aimed to evaluate the impact of tumor microenvironment modulation on the effectiveness of immunotherapy in cancer patients, particularly in enhancing immune responses and improving treatment outcomes. Methods: A total of 112 patients were enrolled in this study at the Department of Radiation Oncology, Mayo Clinic Alix College of Medicine & Health Sciences, from January 2023 to June 2024. Tumor samples were analyzed for TME markers, and patients were treated with immune checkpoint inhibitors combined with TME-modulating agents. Statistical analysis, including t-tests, standard deviation (SD), and p-value calculations, was used to compare clinical outcomes before and after TME modulation. Results: After TME modulation, tumor response rates increased by 45%, with 40% of patients showing complete or partial remission. The standard deviation of tumor shrinkage in the modulated group was 8.2%, compared to 12.5% in the control group, indicating a more consistent response. The p-value for improved survival was 0.03, demonstrating statistical significance in survival benefit between groups. Additionally, the modulated group exhibited a 30% higher infiltration of cytotoxic T lymphocytes (CTLs) into tumors (mean CTLs = 38.7 ± 6.1 in the modulated group versus 26.2 ± 5.4 in the control group). These results indicate that modulating the TME significantly enhances the response to immunotherapy and reduces resistance mechanisms. Conclusion: Targeting the TME offers a promising strategy for improving the efficacy of immunotherapy in cancer treatment, leading to better clinical outcomes and survival rates.
Article Details
Section

This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.