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Biological Therapies in the Treatment of Cancer-Update and New Directions
Monika A Papież1, Wirginia Krzyściak2
1Department of Cytobiology, Faculty of Pharmacy, Jagiellonian University Medical College, 30-688 Kraków, Poland.
Abstract:
Biological therapies have changed the face of oncology by targeting cancerous cells while reducing the effect on normal tissue. This publication focuses mainly on new therapies that have contributed to the advances in treatment of certain malignancies. Immunotherapy, which has repeatedly proven to be a breakthrough therapy in melanoma, as well as B-ALL therapy with CAR T cells, are of great merit in this progress. These therapies are currently being developed by modifying bispecific antibodies and CAR T cells to improve their efficiency and bioavailability. Work on improving the therapy with oncolytic viruses is also progressing, and efforts are being made to improve the immunogenicity and stability of cancer vaccines. Combining various biological therapies, immunotherapy with oncolytic viruses or cancer vaccines is gaining importance in cancer therapy. New therapeutic targets are intensively sought among neoantigens, which are not immunocompromised, or antigens associated with tumor stroma cells. An example is fibroblast activation protein α (FAPα), the overexpression of which is observed in the case of tumor progression. Universal therapeutic targets are also sought, such as the neurotrophic receptor tyrosine kinase (NTRK) gene fusion, a key genetic driver present in many types of cancer. This review also raises the problem of the tumor microenvironment. Stromal cells can protect tumor cells from chemotherapy and contribute to relapse and progression. This publication also addresses the problem of cancer stem cells resistance to treatment and presents attempts to avoid this phenomenon. This review focuses on the most important strategies used to improve the selectivity of biological therapies.
Insights
Biological therapies, including immunotherapy and CAR T-cell therapy, are revolutionizing oncology by targeting cancer cells more precisely. Ongoing research focuses on enhancing these treatments and exploring new targets like FAPα and NTRK gene fusions for improved cancer care.
Area of Science:
- Oncology
- Immunology
- Biotechnology
Background:
- Biological therapies offer targeted cancer treatment with reduced side effects.
- Immunotherapy (e.g., melanoma) and CAR T-cell therapy (e.g., B-ALL) represent significant advancements.
- Current research aims to enhance existing therapies and identify novel targets.
Purpose of the Study:
- To review recent advances in biological therapies for malignancies.
- To highlight strategies for improving the selectivity and efficacy of cancer treatments.
- To discuss challenges such as tumor microenvironment and cancer stem cell resistance.
Main Methods:
- Review of current literature on biological therapies in oncology.
- Analysis of emerging strategies including bispecific antibodies, CAR T-cells, oncolytic viruses, and cancer vaccines.
- Exploration of novel therapeutic targets (neoantigens, FAPα, NTRK gene fusions).
Main Results:
- Immunotherapy and CAR T-cell therapies show significant promise.
- Modifications to bispecific antibodies and CAR T-cells are improving efficiency.
- Oncolytic viruses, cancer vaccines, and combination therapies are under active development.
- Identification of new targets like FAPα and NTRK gene fusions offers broader applicability.
- Understanding the tumor microenvironment and cancer stem cell resistance is crucial.
Conclusions:
- Biological therapies are transforming cancer treatment through enhanced selectivity.
- Continued research into novel targets and combination strategies is essential for overcoming resistance and improving outcomes.
- Addressing the tumor microenvironment and cancer stem cell challenges is key to future therapeutic success.
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