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Clinical Evaluation of Bioadhesive Gels for Oral Cancer Chemoprevention

Primary Purpose

Squamous Cell Carcinoma of Mouth, Intraepithelial Neoplasia

Status
Completed
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
10% FBR containing bioadhesive gel
placebo gel
Sponsored by
Ohio State University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Squamous Cell Carcinoma of Mouth focused on measuring FBR, OSCC, chemoprevention

Eligibility Criteria

21 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Ages: 21 to 80
  2. Microscopically confirmed premalignant oral epithelial disease
  3. No previous history of cancer (with the exception of basal cell carcinoma of the skin)
  4. Tobacco free for at least six weeks prior to entrance in the trial and remain tobacco-free for the three month duration of the study
  5. Availability for necessary study follow-up evaluations (every 10 to 14 days during the trial)
  6. Capable of providing informed consent.

Exclusion Criteria:

  1. Previous history of cancer (with the exception of basal cell carcinoma of the skin)
  2. Current use of tobacco products or refusal to remain tobacco-free for the three month duration of the study
  3. Lack of microscopically confirmed premalignant oral epithelial changes
  4. Microscopic diagnosis of oral squamous cell carcinoma
  5. Previous history of radiation therapy on same side of the head and neck region
  6. History of allergy to any kind of berry
  7. Women who are determined to be pregnant or plan to be pregnant during the trial
  8. Women who are nursing.

Sites / Locations

  • University of Louisville, School of Dentistry
  • University of North Carolina at Chapel Hill
  • The Ohio State University, College of Dentistry

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

10% FBR containing bioadhesive gel

Placebo Gel

Arm Description

Drug consisting of 10% FBR containing bioadhesive gel. Participants instructed to apply 0.5 gm of 10% FBR containing bioadhesive gel four times a day to lesional site

Color/consistency matched placebo (no black raspberry) gel

Outcomes

Primary Outcome Measures

Light Microscopic Histologically Scored Diagnoses Pretreatment to Post Treatment
A hemisection of lesional tissue will be conducted before the 3 month treatment to establish a diagnosis and provide a pretreatment baseline for the experimental parameters. Anl excisional biopsy of the treatment site including any remaining residual lesional tissue (excision of oral dysplastic lesions is consistent with current standards of care) will be obtained after 3 months of treatment to provide a posttreatment diagnosis. The 0 to 8 histologic scale was:0=normal with or without hyperkeratosis BEST OUTCOME, 1=atypia, 2=mild dysplasia, 3=mild-moderate dysplasia, 4=moderate dysplasia,5=moderate-severe dysplasia,6=severe dysplasia, 7=carcinoma in situ, 8=invasive oral squamous cell carcinoma (WORST OUTCOME).

Secondary Outcome Measures

Changes in Lesional Sizes
The remaining oral dysplasia lesion will be inspected at each follow up appointment (every 10-14 days). Biopsies will be immediately conducted on patients with any indication of malignant transformation including indurated, rolled borders, nonhealing ulcers, etc. Accordingly, these patients will withdraw from the trial. Participants will also be monitored for any changes consistent with contact mucositis e.g. soreness and erythema at application site. Clinical photographs were taken for the patients records. Pre treatment and post treatment photographs, with a ruler in place, were used for accurate pre and post treatment size measurement. NOTE: if treatment is beneficial, lesional size will decrease which will be reflected as a negative number.
Treatment Changes in Loss of Heterozygosity Events
Laboratory experiments will be conducted to assess the effects of gel treatment on pre and post loss of heterozygosity (LOH) events at loci associated with tumor suppressor genes.

Full Information

First Posted
August 30, 2010
Last Updated
August 12, 2015
Sponsor
Ohio State University
Collaborators
University of Louisville, University of North Carolina, Chapel Hill, National Cancer Institute (NCI)
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1. Study Identification

Unique Protocol Identification Number
NCT01192204
Brief Title
Clinical Evaluation of Bioadhesive Gels for Oral Cancer Chemoprevention
Official Title
Clinical Evaluation of Bioadhesive Gels for Oral Cancer Chemoprevention
Study Type
Interventional

2. Study Status

Record Verification Date
November 2013
Overall Recruitment Status
Completed
Study Start Date
October 2010 (undefined)
Primary Completion Date
February 2014 (Actual)
Study Completion Date
February 2014 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Ohio State University
Collaborators
University of Louisville, University of North Carolina, Chapel Hill, National Cancer Institute (NCI)

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
This is a multicenter placebo-controlled clinical trial to assess the effects of a topically applied gel on precancerous oral epithelial lesions. A total of 41 participants will be enrolled in this trial, and 22 of them will be enrolled at Ohio State. [The remaining 19 participants will be enrolled at the University of North Carolina (9 participants) and the University of Louisville (8 participants)]. At all three institutions, half of the participants will randomly be assigned to the 10% FBR gel (0.5 gm four times daily for 3 months), while half will enter the placebo control arm. All trial participants will have a pretreatment (including lesional and perilesional tissue) biopsy taken before and an excisional biopsy after 3 months of treatment. As pretreatment indices are compared to post treatment effects on each patient, patients serve as their own internal control. Pretreatment lesional biopsies are obtained to establish a pretreatment diagnosis and provide a pretreatment baseline for the experimental parameters.
Detailed Description
Forty one (41) patients with microscopically confirmed premalignant oral epithelial disease (epithelial dysplasia) will be enrolled in this trial at three clinical centers, i.e. the Ohio State University, University of North Carolina at Chapel Hill and University of Louisville. At all three institutions, half of the participants will randomly be assigned to the 10% FBR gel (0.5 gm four times daily for 3 months), while half will enter the placebo control arm. In accordance with the established standard of care, all participants need to have biopsies taken of their suspicious oral lesions to establish the diagnosis (non research). Trial participants will have three total biopsies. Pretreatment biopsies will entail: 1) perilesional tissue and single saliva sample for FBR metabolic profiling studies (tissue and saliva will be obtained 15 minutes after a single 0.5 gm application of 10% FBR gel for metabolic profiling. Gel application and nonlesional biopsy will be obtained before incisional biopsy of lesional tissue), and 2) a hemisection of lesional tissue to establish a diagnosis and provide a pretreatment baseline for the experimental parameters. While the pretreatment biopsy includes removal of both perilesional and lesional tissue, there will only be one surgical wound as the perilesional tissue is contiguous with the lesional tissue. A final excisional biopsy of the treatment site including any remaining residual lesional tissue (excision of oral dysplastic lesions is consistent with current standards of care) will be obtained after 3 months of treatment. The experimental design permits each patient to serve as their own internal control. Briefly, these following parameters will be monitored in all participants (comparisons made relative to patient-matched pretreatment to posttreatment biopsies): 1) light microscopic diagnoses, 2) clinical appearances and lesional sizes, 3) microarray gene expression analyses, 4) microvascular densities of superficial connective tissues, 5) LOH indices at loci associated with tumor suppressor genes, 6) intraepithelial levels of COX-2 and iNOS protein (image analysis quantified immunohistochemistry), 7) comparison of FBR metabolic profiles relative to extent of chemopreventive efficacy noted.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Squamous Cell Carcinoma of Mouth, Intraepithelial Neoplasia
Keywords
FBR, OSCC, chemoprevention

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 1, Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
41 (Actual)

8. Arms, Groups, and Interventions

Arm Title
10% FBR containing bioadhesive gel
Arm Type
Active Comparator
Arm Description
Drug consisting of 10% FBR containing bioadhesive gel. Participants instructed to apply 0.5 gm of 10% FBR containing bioadhesive gel four times a day to lesional site
Arm Title
Placebo Gel
Arm Type
Placebo Comparator
Arm Description
Color/consistency matched placebo (no black raspberry) gel
Intervention Type
Drug
Intervention Name(s)
10% FBR containing bioadhesive gel
Other Intervention Name(s)
BRB gel
Intervention Description
0.5 gm applied 4 times daily to the oral premalignant lesion site for a duration of 3 months
Intervention Type
Drug
Intervention Name(s)
placebo gel
Other Intervention Name(s)
BRB devoid placebo gel
Intervention Description
0.5 gm applied 4 times daily to the oral premalignant lesion site for a duration of 3 months
Primary Outcome Measure Information:
Title
Light Microscopic Histologically Scored Diagnoses Pretreatment to Post Treatment
Description
A hemisection of lesional tissue will be conducted before the 3 month treatment to establish a diagnosis and provide a pretreatment baseline for the experimental parameters. Anl excisional biopsy of the treatment site including any remaining residual lesional tissue (excision of oral dysplastic lesions is consistent with current standards of care) will be obtained after 3 months of treatment to provide a posttreatment diagnosis. The 0 to 8 histologic scale was:0=normal with or without hyperkeratosis BEST OUTCOME, 1=atypia, 2=mild dysplasia, 3=mild-moderate dysplasia, 4=moderate dysplasia,5=moderate-severe dysplasia,6=severe dysplasia, 7=carcinoma in situ, 8=invasive oral squamous cell carcinoma (WORST OUTCOME).
Time Frame
Before and after the 3 month treatment.
Secondary Outcome Measure Information:
Title
Changes in Lesional Sizes
Description
The remaining oral dysplasia lesion will be inspected at each follow up appointment (every 10-14 days). Biopsies will be immediately conducted on patients with any indication of malignant transformation including indurated, rolled borders, nonhealing ulcers, etc. Accordingly, these patients will withdraw from the trial. Participants will also be monitored for any changes consistent with contact mucositis e.g. soreness and erythema at application site. Clinical photographs were taken for the patients records. Pre treatment and post treatment photographs, with a ruler in place, were used for accurate pre and post treatment size measurement. NOTE: if treatment is beneficial, lesional size will decrease which will be reflected as a negative number.
Time Frame
pretreatment and posttreatment (3 months treatment duration)
Title
Treatment Changes in Loss of Heterozygosity Events
Description
Laboratory experiments will be conducted to assess the effects of gel treatment on pre and post loss of heterozygosity (LOH) events at loci associated with tumor suppressor genes.
Time Frame
Before and after the 3 month treatment duration

10. Eligibility

Sex
All
Minimum Age & Unit of Time
21 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Ages: 21 to 80 Microscopically confirmed premalignant oral epithelial disease No previous history of cancer (with the exception of basal cell carcinoma of the skin) Tobacco free for at least six weeks prior to entrance in the trial and remain tobacco-free for the three month duration of the study Availability for necessary study follow-up evaluations (every 10 to 14 days during the trial) Capable of providing informed consent. Exclusion Criteria: Previous history of cancer (with the exception of basal cell carcinoma of the skin) Current use of tobacco products or refusal to remain tobacco-free for the three month duration of the study Lack of microscopically confirmed premalignant oral epithelial changes Microscopic diagnosis of oral squamous cell carcinoma Previous history of radiation therapy on same side of the head and neck region History of allergy to any kind of berry Women who are determined to be pregnant or plan to be pregnant during the trial Women who are nursing.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Susan R Mallery, DDS, PhD
Organizational Affiliation
Ohio State University
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Louisville, School of Dentistry
City
Louisville
State/Province
Kentucky
ZIP/Postal Code
40202
Country
United States
Facility Name
University of North Carolina at Chapel Hill
City
Chapel Hill
State/Province
North Carolina
ZIP/Postal Code
27599
Country
United States
Facility Name
The Ohio State University, College of Dentistry
City
Columbus
State/Province
Ohio
ZIP/Postal Code
43202
Country
United States

12. IPD Sharing Statement

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Clinical Evaluation of Bioadhesive Gels for Oral Cancer Chemoprevention

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