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Dermatological reactions to the multitargeted tyrosine kinase inhibitor sunitinib
S E Rosenbaum1, S Wu, M A Newman
1Department of Dermatology, Northwestern University, Feinberg School of Medicine, 676 N. St. Clair St., Suite 1600, Chicago, IL 60611, USA.
Background:
The multikinase inhibitor sunitinib has enhanced the treatment of renal cell carcinoma and gastrointestinal stromal tumor through an improved clinical response with decreased systemic toxicities. However, sunitinib is frequently associated with dermatological adverse reactions. The physical and psychosocial impact of frequent dermatological toxicities can affect consistent antineoplastic therapy and quality of life.
Patients And Methods:
Dermatological adverse reaction information was compiled from Pfizer Medical Information and from abstracts from the 2007 American Society of Clinical Oncology annual meeting, Prostate Cancer Symposium, and Gastrointestinal Cancers Symposium. Published clinical trials of sunitinib in MEDLINE, Cochrane Library, Cochrane Controlled Trials Register, and EMBASE Drugs and Pharmacology databases were also included. Information was accessed on or before June 30, 2007.
Results:
In the pooled analysis, all-grade hand-foot skin reaction occurred in 19% of patients (5% grades 3-4), skin discoloration in 28% (0% grades 3-4), dry skin in 16% (1% grades 3-4), skin rash in 13% (1% grades 3-4), dermatitis in 8% (2% grades 3-4), hair color changes in 10% (0% grades 3-4), alopecia in 6% (0% grades 3-4), and phototoxicity in <0.1%.
Conclusions:
Dermatological reactions associated with sunitinib occur frequently. Evidence-based treatment recommendations are needed in order to maximize quality of life and optimize clinical outcome.
Insights
Sunitinib, a multikinase inhibitor, effectively treats cancers but frequently causes skin issues. Managing these dermatological side effects is crucial for patient quality of life and treatment adherence.
Area of Science:
- Oncology
- Dermatology
- Pharmacology
Background:
- Sunitinib is a multikinase inhibitor used for renal cell carcinoma and gastrointestinal stromal tumors.
- While effective, sunitinib frequently causes dermatological adverse reactions.
- These skin toxicities can negatively impact patient quality of life and treatment adherence.
Purpose of the Study:
- To review and summarize the incidence and types of dermatological adverse reactions associated with sunitinib.
- To highlight the need for evidence-based recommendations for managing these side effects.
Main Methods:
- Information was gathered from Pfizer Medical Information and major oncology conference abstracts (2007).
- A comprehensive literature search was conducted using MEDLINE, Cochrane Library, and EMBASE databases.
- Data was accessed up to June 30, 2007.
Main Results:
- Hand-foot skin reaction occurred in 19% of patients (5% grade 3-4).
- Skin discoloration (28%), dry skin (16%), and skin rash (13%) were also common.
- Other reactions included dermatitis (8%), hair color changes (10%), alopecia (6%), and phototoxicity (<0.1%).
Conclusions:
- Dermatological reactions are a frequent occurrence with sunitinib treatment.
- Effective management strategies are necessary to improve patient outcomes and quality of life.
- Further research is needed to develop evidence-based treatment guidelines for sunitinib-induced dermatological toxicities.
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