TY - JOUR
T1 - Bacillus Calmette-Guérin (BCG) and Interferon (IFN) Gene Therapy for Combination Bladder Cancer Treatment
T2 - A Mathematical Model for Improved Efficacy and Tolerability
AU - Bunimovich-Mendrazitsky, Svetlana
AU - O'Donnell, Michael A.
AU - Halachmi, Sarel
AU - Kronik, Natalie
N1 - Publisher Copyright:
© 2025 Wiley-VCH GmbH.
PY - 2025
Y1 - 2025
N2 - Intravesical instillation of Bacillus Calmette-Guérin (BCG) bacteria represents the gold standard adjuvant therapy for non-muscle-invasive bladder cancer following tumor resection. Despite treatment efficacy, ≈50% of patients exhibit resistance to treatment or cannot complete the therapeutic course due to severe side effects. Nadofaragene firadenovec (IFN-gene) therapy, recently FDA-approved for BCG-unresponsive patients, offers potential benefits by utilizing intravesical adenoviral infection to produce high local IFNα levels sustained for several days. By simulating changes in treatment protocols, mathematically, how combining these agents may provide more effective and better-tolerated regimens for BCG non-responder or intolerant patients is explored. Four equations are employed to model the dynamics of tumor cells, immune system responses, and BCG with IFN-gene therapy interactions. The model predicts that improved outcomes, compared to basic protocols, can be achieved. Specifically, combining BCG and IFN-gene therapy reduces the non-responder rate from 52% to 32%. Moreover, reducing BCG dosage while combining it with IFN-gene therapy in prolonged maintenance courses with five additional treatment cycles reduces non-responders to 10%. IFN-gene therapy creates stable windows of opportunity for enhanced immune system responses, achieving improved BCG-stimulated malignant urothelial cell killing. The protocol assists future rational clinical trial planning to test these hypotheses.
AB - Intravesical instillation of Bacillus Calmette-Guérin (BCG) bacteria represents the gold standard adjuvant therapy for non-muscle-invasive bladder cancer following tumor resection. Despite treatment efficacy, ≈50% of patients exhibit resistance to treatment or cannot complete the therapeutic course due to severe side effects. Nadofaragene firadenovec (IFN-gene) therapy, recently FDA-approved for BCG-unresponsive patients, offers potential benefits by utilizing intravesical adenoviral infection to produce high local IFNα levels sustained for several days. By simulating changes in treatment protocols, mathematically, how combining these agents may provide more effective and better-tolerated regimens for BCG non-responder or intolerant patients is explored. Four equations are employed to model the dynamics of tumor cells, immune system responses, and BCG with IFN-gene therapy interactions. The model predicts that improved outcomes, compared to basic protocols, can be achieved. Specifically, combining BCG and IFN-gene therapy reduces the non-responder rate from 52% to 32%. Moreover, reducing BCG dosage while combining it with IFN-gene therapy in prolonged maintenance courses with five additional treatment cycles reduces non-responders to 10%. IFN-gene therapy creates stable windows of opportunity for enhanced immune system responses, achieving improved BCG-stimulated malignant urothelial cell killing. The protocol assists future rational clinical trial planning to test these hypotheses.
KW - BCG therapy
KW - Nadofaragene firadenovec gene therapy (IFN-gene)
KW - immune system cell dynamics
KW - immunotherapy
KW - ordinary differential equations (ODE)
UR - https://www.scopus.com/pages/publications/105019800707
U2 - 10.1002/adts.202501147
DO - 10.1002/adts.202501147
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AN - SCOPUS:105019800707
SN - 2513-0390
JO - Advanced Theory and Simulations
JF - Advanced Theory and Simulations
ER -