Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
4
pubmed:dateCreated
2011-7-8
pubmed:abstractText
Gefitinib is an inhibitor of the epidermal growth factor receptor, which is frequently expressed on both choroidal and nonchoroidal melanoma cells. We evaluated the clinical efficacy of gefitinib in patients with metastatic melanoma. Patients with stage IV or unresectable stage III melanoma and Zubrod performance status of less than or equal to 2 were eligible. Previous systemic treatment for metastatic disease was required. The dose of oral gefitinib was 250 mg administered daily, and tumor response was evaluated every 6 weeks. Forty-six patients with nonchoroidal melanoma and six with choroidal melanoma were treated, and 48 were evaluable for response. The median age was 62.5 years. Forty-one patients (79%) had stage M1c disease. There were no drug-related grade 4 or 5 adverse events, and fatigue was the only grade 3 adverse event that occurred in more than 5% of patients. Two patients (4%) had partial responses and 13 patients (27%) had disease stabilization. The two responders had a median duration of response of 10.9 months. The median overall progression-free survival was 1.4 months and the median overall survival was 9.7 months. Among the patients with sufficient tissues obtained before and 6 weeks after starting gefitinib administration, there were no notable trends in the changes of the tumoral expression of p-ERK1/2, p-AKT, PAK1, and serum levels of vascular endothelial growth factor or IL-8 with treatment. We concluded that gefitinib was well tolerated but had minimal clinical efficacy as a single-agent therapy for unselected patients with metastatic melanoma.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Aug
pubmed:issn
1473-5636
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
21
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
357-63
pubmed:meshHeading
pubmed-meshheading:21738104-Administration, Oral, pubmed-meshheading:21738104-Adult, pubmed-meshheading:21738104-Aged, pubmed-meshheading:21738104-Aged, 80 and over, pubmed-meshheading:21738104-Antineoplastic Agents, pubmed-meshheading:21738104-Choroid Neoplasms, pubmed-meshheading:21738104-Disease-Free Survival, pubmed-meshheading:21738104-Female, pubmed-meshheading:21738104-Humans, pubmed-meshheading:21738104-Male, pubmed-meshheading:21738104-Melanoma, pubmed-meshheading:21738104-Middle Aged, pubmed-meshheading:21738104-Mutation, pubmed-meshheading:21738104-Neoplasm Staging, pubmed-meshheading:21738104-Protein Kinase Inhibitors, pubmed-meshheading:21738104-Quinazolines, pubmed-meshheading:21738104-Receptor, Epidermal Growth Factor, pubmed-meshheading:21738104-Texas, pubmed-meshheading:21738104-Time Factors, pubmed-meshheading:21738104-Treatment Outcome, pubmed-meshheading:21738104-Young Adult
pubmed:year
2011
pubmed:articleTitle
A phase II study of gefitinib in patients with metastatic melanoma.
pubmed:affiliation
Department of Melanoma Medical Oncology, The University of Texas M.D. Anderson Cancer Center, Houston, Texas 77030, USA.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't, Clinical Trial, Phase II, Research Support, N.I.H., Extramural