Cancer Vaccines and Oncolytic Viruses Exert Profoundly Lower Side Effects in Cancer Patients than Other Systemic

Volker Schirrmacher1

  • 1Immune-Oncological Center Cologne (IOZK), D-50674 Cologne, Germany.

Biomedicines
|March 20, 2020
PubMed

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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