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Paramyxoviruses for Tumor-targeted Immunomodulation: Design and Evaluation Ex Vivo
Published on: January 7, 2019
Cancer Vaccines and Oncolytic Viruses Exert Profoundly Lower Side Effects in Cancer Patients than Other Systemic
1Immune-Oncological Center Cologne (IOZK), D-50674 Cologne, Germany.
Abstract:
This review compares cytotoxic drugs, targeted therapies, and immunotherapies with regard to mechanisms and side effects. Targeted therapies relate to small molecule inhibitors. Immunotherapies include checkpoint inhibitory antibodies, chimeric antigen receptor (CAR) T-cells, cancer vaccines, and oncolytic viruses. All these therapeutic approaches fight systemic disease, be it micro-metastatic or metastatic. The analysis includes only studies with a proven therapeutic effect. A clear-cut difference is observed with regard to major adverse events (WHO grades 3-4). Such severe side effects are not observed with cancer vaccines/oncolytic viruses while they are seen with all the other systemic therapies. Reasons for this difference are discussed.
Insights
This review compares cytotoxic drugs, targeted therapies, and immunotherapies for cancer treatment. Cancer vaccines and oncolytic viruses show fewer severe side effects compared to other systemic therapies.
Area of Science:
- Oncology
- Pharmacology
- Immunology
Background:
- Systemic therapies like cytotoxic drugs, targeted therapies, and immunotherapies are crucial for treating metastatic and micro-metastatic cancers.
- Understanding the mechanisms and side effect profiles of these treatments is essential for optimizing patient care.
Purpose of the Study:
- To compare the mechanisms and side effects of cytotoxic drugs, targeted therapies (small molecule inhibitors), and various immunotherapies.
- To analyze the incidence of major adverse events (WHO grades 3-4) across these different therapeutic modalities.
Main Methods:
- Review of studies with proven therapeutic effects on systemic cancer disease.
- Comparative analysis of reported major adverse events (WHO grades 3-4) for cytotoxic drugs, targeted therapies, and immunotherapies.
- Categorization of immunotherapies including checkpoint inhibitory antibodies, CAR T-cells, cancer vaccines, and oncolytic viruses.
Main Results:
- All analyzed systemic therapies, including cytotoxic drugs, targeted therapies, and immunotherapies (checkpoint inhibitors, CAR T-cells), are associated with major adverse events.
- Cancer vaccines and oncolytic viruses, a subset of immunotherapies, did not show severe side effects (WHO grades 3-4) in the reviewed studies.
- A distinct difference in the occurrence of severe adverse events was observed between cancer vaccines/oncolytic viruses and other systemic treatments.
Conclusions:
- Cancer vaccines and oncolytic viruses represent a safer alternative regarding severe adverse events compared to cytotoxic drugs, targeted therapies, and other immunotherapies.
- The differing safety profiles warrant further investigation into the underlying mechanisms responsible for the observed side effect differences.
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