A Phase 1 interventional study of sirolimus and comparative genomic hybridization in Neoplastic Syndrome and Non-melanomatous Skin Cancer, sponsored by Yale University. Completed. Open to participants aged 18 Years to 120 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2016-09-23.
Sponsored by Yale University · Phase 1, Interventional, and Prevention
RATIONALE: Studying samples of blood and tissue from patients with basal cell nevus syndrome and from healthy participants in the laboratory may help doctors learn more about changes that may occur in DNA and identify biomarkers related to basal cell nevus syndrome. Chemoprevention is the use of certain drugs to keep cancer from forming, growing, or coming back. The use of sirolimus may keep basal cell skin cancer from forming in patients with basal cell nevus syndrome.
PURPOSE: This phase I trial is studying topical sirolimus in patients with basal cell nevus syndrome and in healthy participants.
OBJECTIVES:
Primary
OUTLINE: Patients and healthy participants receive topical sirolimus ointment twice daily for 12 weeks.
Blood and skin biopsies are obtained at baseline and at week 12 for gene and protein expression studies. Alterations in RNA are measured by microarray analysis. Alterations in protein expression are measured by 2-dimensional gel electrophoresis and matrix-assisted laser desorption ionization time-of-flight mass spectrometry.
After completion of study therapy, patients and healthy participants are followed at 4 weeks.
PROJECTED ACCRUAL: A total of 16 patients and healthy participants will be accrued for this study.
9,610 studies on the registry are indexed under Neoplasms; 2,508 are open to participants now.
This study's planned enrollment of 16 is below the median of 50 across 7,429 interventional studies indexed under Neoplasms.
Browse Neoplasms studies →Yale University is the lead sponsor of 1,763 studies on the registry; 292 are open to participants now.
Of its 217 completed or terminated interventional studies of FDA-regulated products, 128 (59%) have results posted.
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DISEASE CHARACTERISTICS:
Patient
Known patched (PTCH) gene mutation
Age- and sex-matched healthy participant (control)
Unaffected relative of patient OR normal healthy volunteer with no family history of BCNS or features of BCNS
No unrelated healthy participant meeting any of the following clinical criteria for BCNS:
No unrelated healthy participant with 2 or more of the following features:
PATIENT CHARACTERISTICS:
PRIOR CONCURRENT THERAPY:
No drugs or substances that would effect sirolimus blood concentrations, including any of the following:
Alterations in RNA as measured by microarray analysis
Alterations in protein expression as measured by 2-dimensional gel electrophoresis and matrix-assisted laser desorption ionization time-of-flight mass spectroscopy
No study locations are listed for this record.
This study is completed, as verified in Sep 2016. You cannot join it, but the record below documents what was studied.
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Studies of the drug tested here: Sirolimus