CCI‐779 in metastatic melanoma
Top Cited Papers
- 8 July 2005
- Vol. 104 (5) , 1045-1048
- https://doi.org/10.1002/cncr.21265
Abstract
BACKGROUND CCI‐779 is an analog of the immunosuppressive agent, rapamycin, that has demonstrated activity against melanoma in preclinical models and shown clinical benefit in patients with breast and renal carcinoma. CCI‐779 is not immunosuppressive when administered on an intermittent schedule, and its toxicity is modest, consisting of nausea, diarrhea, hypertriglyceridemia, thrombocytopenia, asthenia, and follicular dermatitis. METHODS The current trial was designed to detect a median time to disease progression of >18 weeks in patients with metastatic melanoma treated with a 250‐mg weekly dose of CCI‐779 administered intravenously after diphenhydramine premedication. Patients with measurable disease, no more than one previous chemotherapy regimen for metastatic disease, and normal organ function were eligible, and patients with central nervous system involvement, P450‐inducing or P450‐suppressing drugs, or hypertriglyceridemia were excluded. RESULTS Thirty‐three patients (21 males) were treated, 21 of whom had been treated previously with chemotherapy and/or biologic agents for advanced‐stage disease. One patient had a partial response lasting 2 months. The median time to disease progression and overall survival were 10 weeks and 5 months, respectively. Toxicity was mild and predominantly mucocutaneous (stomatitis, diarrhea, and rash). Hyperlipidemia was cumulative and was managed with lipid‐lowering agents. CONCLUSIONS CCI‐779 was not sufficiently active in melanoma to warrant further testing as a single agent. Cancer 2005. © 2005 American Cancer Society.Keywords
This publication has 9 references indexed in Scilit:
- Randomized Phase II Study of Multiple Dose Levels of CCI-779, a Novel Mammalian Target of Rapamycin Kinase Inhibitor, in Patients With Advanced Refractory Renal Cell CarcinomaJournal of Clinical Oncology, 2004
- AKT Activity Determines Sensitivity to Mammalian Target of Rapamycin (mTOR) Inhibitors by Regulating Cyclin D1 and c-myc ExpressionJournal of Biological Chemistry, 2004
- Uncommon Presentations of Hodgkin's DiseaseJournal of Clinical Oncology, 2004
- Src Family Protein-tyrosine Kinases Alter the Function of PTEN to Regulate Phosphatidylinositol 3-Kinase/AKT CascadesJournal of Biological Chemistry, 2003
- Targeting mTOR signaling for cancer therapyCurrent Opinion in Pharmacology, 2003
- Mechanisms of resistance to rapamycinsDrug Resistance Updates, 2001
- Enhanced sensitivity of PTEN-deficient tumors to inhibition of FRAP/mTORProceedings of the National Academy of Sciences, 2001
- The rapamycin-sensitive signal transduction pathway as a target for cancer therapyOncogene, 2000
- TOR, a Central Controller of Cell GrowthCell, 2000