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Potentiation of Anticancer Antibody Efficacy by Antineoplastic Drugs: Detection of Antibody-drug Synergism Using the Combination Index Equation
Published on: January 19, 2019
Skin reactions to the new biologic anticancer drugs
Patricia L Myskowski1, Allan C Halpern
1Dermatology Service, Department of Medicine, Memorial Sloan-Kettering Cancer Center, New York, New York, USA. myskowsp@mskcc.org
Purpose Of Review:
To review the clinical presentation and management of cutaneous side effects of some of the new targeted anticancer therapies.
Recent Findings:
Advances in molecular biology have led to the development of pharmacologic agents that specifically target crucial molecules on malignant cells, or their surrounding cellular milieu (e.g. angiogenesis inhibitors), or both. Successful treatments for several solid tumors, including colorectal carcinoma, nonsmall cell lung cancer, head and neck cancer and renal cell carcinoma, have recently been implemented as a result of these advances. Although these agents are generally much better tolerated than their cytotoxic predecessors, new groups of side effects have emerged, especially with regard to the skin. Multikinase inhibitors, monoclonal antibodies, and - in particular - antiepidermal growth factor inhibitors are associated with cutaneous reactions that may not only be dose limiting, but may significantly affect quality of life. The spectrum of these reactions ranges from disfiguring acneiform facial eruptions, to impaired wound healing, to disabling hand-foot syndromes, which can seriously impair mobility.
Summary:
The recognition, prevention and management of the cutaneous side effects of these targeted agents can allow successful continuation of antineoplastic therapy, and minimize patient distress.
Insights
New targeted anticancer therapies can cause significant skin side effects, impacting treatment continuation and quality of life. Early recognition and management of these cutaneous reactions are crucial for patient well-being.
Area of Science:
- Oncology
- Dermatology
- Molecular Biology
Background:
- Targeted anticancer therapies, developed through molecular biology advances, offer new treatment options for solid tumors.
- These novel agents target specific molecules in cancer cells or their microenvironment, such as angiogenesis inhibitors.
- While generally better tolerated than traditional chemotherapy, these therapies introduce unique side effect profiles, particularly affecting the skin.
Purpose of the Study:
- To review the clinical presentation of skin side effects associated with new targeted anticancer therapies.
- To outline the management strategies for these cutaneous adverse events.
- To emphasize the importance of addressing these side effects for treatment adherence and patient quality of life.
Main Methods:
- Literature review of clinical presentations and management of cutaneous side effects.
- Analysis of side effect profiles associated with specific targeted therapy classes, including multikinase inhibitors, monoclonal antibodies, and anti-epidermal growth factor inhibitors.
- Synthesis of information on the impact of these reactions on treatment outcomes and patient well-being.
Main Results:
- Targeted therapies, particularly antiepidermal growth factor inhibitors, are linked to a range of cutaneous reactions.
- These reactions include acneiform eruptions, impaired wound healing, and hand-foot syndromes, which can be dose-limiting and affect mobility.
- The severity of these skin toxicities can significantly impact a patient's quality of life and necessitate treatment modifications.
Conclusions:
- Effective recognition, prevention, and management of skin side effects are essential for continuing targeted anticancer therapy.
- Addressing these cutaneous reactions can minimize patient distress and improve overall treatment outcomes.
- Proactive dermatological care is vital for patients undergoing treatment with novel targeted anticancer agents.
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