Molecular targeted therapies for solid tumors: management of side effects
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Updated: Jun 24, 2026

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Published on: June 16, 2023
Viktor Grünwald1, Jens Soltau, Philipp Ivanyi
1Klinik für Hamatologie, Hämostaseologie, Onkologie und Stammzelltransplantation, Medizinische Hochschule Hannover, Germany.
Abstract:
This review will provide physicians and oncologists with an overview of side effects related to targeted agents that inhibit vascular endothelial growth factor (VEGF), epidermal growth factor (EGF) and mammalian target of rapamycin (mTOR) signaling in the treatment of solid tumors. Such targeted agents can be divided into monoclonal antibodies, tyrosine kinase inhibitors, multitargeted tyrosine kinase inhibitors and serine/threonine kinase inhibitors. Molecular targeted therapies are generally well tolerated, but inhibitory effects on the biological function of the targets in healthy tissue can result in specific treatment-related side effects, particularly with multitargeted agents. We offer some guidance on how to manage adverse events in cancer patients based on the range of options currently available.
Insights
This review discusses side effects of targeted cancer therapies, including those inhibiting vascular endothelial growth factor (VEGF), epidermal growth factor (EGF), and mammalian target of rapamycin (mTOR). It offers guidance for managing adverse events in patients undergoing treatment for solid tumors.
Area of Science:
- Oncology
- Pharmacology
- Molecular Biology
Background:
- Targeted therapies offer novel treatment strategies for solid tumors.
- Inhibitors of vascular endothelial growth factor (VEGF), epidermal growth factor (EGF), and mammalian target of rapamycin (mTOR) signaling are key molecular agents.
- Understanding their side effect profiles is crucial for effective clinical management.
Purpose of the Study:
- To provide an overview of side effects associated with targeted agents.
- To categorize targeted agents based on their mechanisms of action.
- To offer guidance on managing adverse events in cancer patients.
Main Methods:
- Review of literature on targeted therapies for solid tumors.
- Classification of targeted agents into monoclonal antibodies, tyrosine kinase inhibitors, multitargeted tyrosine kinase inhibitors, and serine/threonine kinase inhibitors.
- Synthesis of information on common and specific side effects.
Main Results:
- Molecular targeted therapies are generally well tolerated.
- Inhibition of VEGF, EGF, and mTOR pathways can lead to specific side effects in healthy tissues.
- Multitargeted agents may present a higher incidence of adverse events.
- Specific side effects are linked to the targeted pathways and drug class.
Conclusions:
- Targeted therapies, while effective, require careful monitoring for side effects.
- Management strategies for adverse events are available and essential for patient care.
- Personalized treatment approaches considering potential toxicities are important in oncology.
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