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This study presented a glioma growth model that accounts for drug-sensitive and drug-resistant cells in response to chemotherapy and anti-angiogenic therapy. Chemotherapy induces mutations in drug-sensitive cells, leading to the emergence of drug-resistant cells and highlighting the benefits of combined therapy. Anti-angiogenic therapy can mitigate mutations by inducing angiogenic dormancy. We have identified two reproduction numbers associated with the non-cell and disease-free states. Numerical sensitivity analysis has highlighted influential parameters that control glioma growth dynamics, emphasizing the interactions between drug-sensitive and drug-resistant cells. To reduce glioma endemicity among sensitive cases, it was recommended to decrease chemotherapy expenditure, increase angiogenic dormancy, and adjust chemotherapy infusion rates. In addition, to combat resistance to glioma endemicity, enhancing angiogenic dormancy is crucial.
This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0)
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