Please login or create an account. If you do not have access to this content, you will be shown a 30 second preview and licensing options.
- Presentation
Cutaneous Side Effects of Oncology Drugs: Part 2 - Targeted Therapy and Immunotherapy
Description
Doctor Connie XI continued the discussion on cutaneous side effects of oncology drugs, focusing on targeted therapy and immunotherapy. She highlighted the increasing number of oncology therapies and their associated skin side effects, emphasizing the role of dermatologists in managing these issues to maintain patient quality of life and medication adherence. Key topics included epidermal growth factor receptor (EGFR) inhibitors, such as amivantamab, which has significant cutaneous toxicities like acneiform rashes and scalp issues. Treatments for these conditions involve employing emollients, topical steroids, and antibiotics, and in severe cases, systemic retinoids or dose adjustments may be necessary. Additionally, she explored antibody drug conjugates like infortumab vedotin, which can cause skin toxicities due to targets also present in normal skin, and discussed management strategies for these reactions, which can resemble toxic erythema from chemotherapy. Another category covered was bispecific T cell engagers, particularly those used for multiple myeloma, where skin and oral mucosal toxicities are prevalent. XI reiterated the importance of recognizing and managing these adverse effects effectively, to ensure that patients can continue their critical cancer therapies.
View moreConclusions
- Targeted therapies and immunotherapy are increasingly associated with various cutaneous side effects.
- EGFR inhibitors, particularly newer agents like amivantamab, show a high prevalence of skin toxicities, including acneiform rashes and paronychia.
- Treatment strategies for acneiform eruptions include the use of emollients, topical steroids, and oral antibiotics, avoiding topical retinoids due to increased dryness.
- Skin toxicities from antibody-drug conjugates, such as enfortumab vedotin, are common and immediate, with skin effects appearing within two weeks of starting therapy.
- Severe skin reactions from enfortumab may necessitate dose adjustments or treatment discontinuation.
- Management of oral mucosal toxicities with bispecific T-cell engagers like talquetamab includes usage of saliva substitutes, dietary adjustments, and pain management.
- Prompt recognition and supportive care for dermatologic events can help maintain patients' oncology treatment compliance and quality of life.
- Huynh Dagher S et al. Int J Womens Dermatol. 2021
- Aw DCW et al. Asia-Pacific Journal of Clinical Oncology 2017
- Fabroccini et al. Skin Appendage Disord. 2015
- Vigarios E et al. Support Care Cancer 2017
- Arana I *, Riew GJ *, Rock A, Nambudiri VE, Modi B *, Shi CR *. JAAD 2025
- Belzer A *, Nguyen MO *, Talsania A, Haldas J, Smith J *, Leventhal JS *. JAMA Dermatol. 2023
- Huang PW, Yu CJ, Yang JC, Chu CY. Lung Cancer 2024
- Muhaj FF, Tran J, Dai J, Pacha O, Patel AB. JAAD Case Reports 2024
- Enescu CD et al. JAAD Case Rep. 2022
- Einsele H et al. Cancer 2020
- Lacouture ME et al. The Oncologist 2022
- Geraud A et al. Eur J Cancer 2024
- Lery M, Perrot A, Ortiz-Brugués A, Vigarios E, Anghel D, Bories P, Sibaud V. JAAD 2024
- Mancia SS et al. Blood 2021.