Wild Type p53 Adenovirus for Oral Premalignancies
- To determine the maximum tolerated dose and transduction efficiency of adenoviral mediated wild type p53 gene transfer in premalignancies of the upper aerodigestive tract.
- To determine the efficacy of single agent adenoviral mediated wild type p53 gene transfer in reversing oral premalignancies.
|Study Design:||Endpoint Classification: Safety/Efficacy Study
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Treatment
|Official Title:||Clinical Protocol for Wild Type p53 Gene Induction in Premalignancies of Squamous Epithelium of the Oral Cavity and Oral Pharynx Via an Adenoviral Vector [NCI Supplied Agent Ad-p53, (INGN 201) (Advexin®) NSC 683550, IND# 7135]|
- Maximum Tolerated Dose (MTD) of INGN 201 [ Time Frame: Following 1 week of experimental treatment in each 4 week course ] [ Designated as safety issue: Yes ]MTD is defined as the highest dose level at which there are less than or equal to 1/6 patients with a dose limiting toxicity (DLT).
|Study Start Date:||June 2003|
|Study Completion Date:||November 2010|
|Primary Completion Date:||March 2008 (Final data collection date for primary outcome measure)|
Experimental: INGN 201
INGN201 injection + oral rinse, day 1, courses 1-6. Twice-daily oral rinses, days 2-5, courses 1-6.
Genetic: INGN 201
Mouth rinse given one time on the first day and two times on Days 2-5 of each course of INGN 201. The injection and rinse (first day of each cycle), or the two rinses (Days 2-5 of each cycle), will be separated by at least two hours.
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Some cancers that occur in the mouth may in some way be due to a defect in a gene called the p53 gene. In this study, an adenovirus is used as a tool (a "vector") to deliver the normal p53 gene into cells. The parts of the adenovirus that allow it to reproduce and promote infection are removed, and the experimental gene (p53) is added.
Prior to beginning this study, all participants will have a complete medical history and physical exam, including measurement of vital signs and weight. Participants will have an electrocardiogram (ECG), a urine test, and blood tests, including an HIV test. At mid-cycle, another white blood cell count will have to be drawn. Women able to have children must have a negative blood pregnancy test. Participants will be asked what medications have been taken in the past 30 days. Additionally, a chest x-ray will be performed.
All participants will undergo a complete head and neck examination. This includes both visual [direct as well as mirror (and fiberoptic if required)] of all mucosal sites from the nasal and lip areas to the back of the throat. The physician will manually examine areas of the skin, salivary glands, the neck, and thyroid bed. Also, the doctor will make sure the cranial nerves are working properly. Location and size of lesion(s) will be recorded and measured in two dimensions. All lesions present will be photographed prior to the start of the intervention.
Physical examination including a fiberoptic exam, is the established standard of evaluating pre-cancerous lesion(s). Only if a concern for cancer is present , or symptoms are beyond those findings of the physical examination will a CT or MRI be prescribed. These tests (CT and MRI) should not have to be done since they have no established role in the evaluation, management, or follow-up of these lesion(s). If utilized, a CT (computerized tomography) scan is a special test using x-ray along with a computer to give detailed pictures of parts of the body. An MRI (magnetic resonance imaging) is a special test using a strong magnetic field and radio frequency signals to give detailed pictures of parts of the body. An x-ray shows a 2-dimensional picture while a CT scan or an MRI shows 3 dimensions.
Each study course includes one week of treatment followed by three weeks of observation. The length of the study is 6 months (6 courses) for most participants. Participants will return to the clinic twice a day for Days 2 - 5 for each month of participation, and should expect to spend a total of about 6 hours a day at the clinic.
Participants in this study will receive INGN 201 in two ways. The first way will be by injection in the area of the lesion. The second way will be by mouth rinse. Vital signs will be checked each time before participants receive INGN 201. The injection will be given on the first day of each week of the course, after a numbing (anesthetic) medication is applied to prevent discomfort.
The mouth rinse will be given one time on the first day and two times on Days 2 - 5 of each course of INGN 201. The injection and rinse (first day of each cycle), or the two rinses (Days 2 - 5 of each cycle), will be separated by at least two hours. There will be a 30 second rinse with 5% acetic acid, a raspberry flavored, vinegar-like liquid, followed by a tap water rinse just before participants receive INGN 201. Participants will be asked to hold the INGN 201 in their mouth for 30 minutes. Eating and drinking should be avoided for one hour after receiving the mouth rinse. The injection and rinse series will be repeated on a monthly basis for a period of six months.
Participants will be requested to have two biopsies (small tissue samples) of the premalignant lesion taken on Day 5 of the 1st and 6th courses. These biopsies will contribute to the understanding of how the experimental agent works on pre-cancerous cells. In particular, the biopsies will help to determine if the experimental agent is effective in killing pre-cancerous cells (this process is called apoptosis). These studies will also determine if the gene therapy injections have been effective in delivering the gene (p53) to the precancerous cells.
Participants will be observed for three more weeks after the sixth course of treatment. At the end of the study, 28 days after the last dose of INGN 201, participants will have a physical exam, including measurement of weight and vital signs. Participants will have a medical history and blood and urine tests. These tests are done to monitor the effects of the study treatment.
Participants who develop severe side effects will be taken off study, though they may continue to receive follow-up evaluations to monitor their health. Participants will be counseled by their physician should the lesion(s) progress to cancer during the study or follow up period. After counseling, participant may choose to have surgery to remove the precancerous lesion(s), laser surgery, or observation. The participant will then be monitored closely.
Study participants will be followed for five years, and must agree to stay in contact with their personal doctor or the doctor responsible for this study even if they move after the study ends. The participant's personal doctor may be asked to provide information about any anticancer treatments received after the study's completion, as well as information about the patient's overall health.
This is an investigational study. This experimental use of human genes is an example of gene therapy. This is the first time that adenovirus gene therapy has been used for a pre-cancerous condition. This is the first study to use INGN 201 as a mouth rinse. A total of 20 patients will be enrolled at M. D. Anderson. A maximum of 51 subjects will be entered in this multi-center study.
Please refer to this study by its ClinicalTrials.gov identifier: NCT00410865
|United States, Texas|
|UT MD Anderson Cancer Center|
|Houston, Texas, United States, 77030|
|Principal Investigator:||Gary L. Clayman, MD||U.T. MD Anderson Cancer Center|