Actinic Keratosis
Conditions
Brief summary
The purpose of this research is to obtain a blood sample from patients with actinic keratoses undergoing routine Photodynamic Therapy, in order to measure biomarkers that are relevant to VitD and 5FU metabolism and might be predictive of PDT outcome. The biomarkers to be examined include serum VitD levels at the time of PDT, and the presence/absence of gene alleles that correlate with expression of several proteins involved in VitD and 5FU metabolism. The presence of these biomarkers will be correlated to the improvement in AK lesion counts at the patient's routine follow-up visit 3 months after PDT treatment.
Detailed description
Patients who have been scheduled to receive PDT in our noninvasive cutaneous oncology clinics will be given written information prior to their visit, including a copy of the Informed Consent (IC) that describes the purpose of the study. If the patient indicates that he/she is interested, the physician or study nurse will review the IC with the patient on the day of PDT and answer all questions. After the patient signs the IC, the patient will have their blood drawn by a caregiver who has completed PTS Phlebotomy Training. DNA samples will be stored in a locked minus 80 degree ultrafreezer, in Dr. Maytin's laboratory (room ND4-25A in the Lerner Research Institute). The samples will be maintained for up to 10 years. Blood sample tubes and data sheets in the laboratory will be labeled with a code consisting of the first 5 digits of the patient's 8-digit MRN along with the date that the phlebotomy was performed (i.e. the date of the blood draw). This should ensure anonymity of the data while preventing mistakes when linking the laboratory results to the correct patient. Study personnel with password-protected access to the database registry will use the code to unequivocally identify the subject's file within the Oracle database and thereby enter the subject's laboratory results into the proper data field. The Informed Consent document informs the subject that he/she can withdraw permission for use of their samples at any time, and explains how to do this by contacting the Principal Investigator (PI) in writing. Information will not be disclosed to third party outside of Cleveland Clinic for research purposes.
Interventions
None listed
Sponsors
The Cleveland Clinic
Study design
Observational model
CASE_ONLY
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Males or females, at least 18 years of age * Patient has nonhypertrophic actinic keratosis, at least 10 AK lesions present on the face, scalp, forearms, chest, or legs at the time of PDT treatment
Exclusion criteria
* taking doxycline, a photosensitizer * using topical retinoids, since these can exacerbate the post-PDT erythema reaction * pregnant
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Actinic Keratosis (AK) clearance | at 3 months post-treatment | Change in AK lesions present at 3 months post-PDT treatment |
| Vitamin D levels | At baseline, which is the day of PDT treatment | Vitamin D level (25-hydroxy-cholecalciferol) measured in serum |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Allele polymorphisms in the gene of the Vitamin D receptor (VDR) | At baseline, which is the day of PDT treatment | Identify the allele combination present at VDR locus |
| Allele polymorphisms in the gene promoter of thymidylate synthase (TS) enzyme | At baseline, which is the day of PDT treatment | Identify the allele combination present at TS locus |
Countries
United States
Outcome results
None listed