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Chemoprevention Study of Oral Cavity Squamous Cell Carcinoma

Primary Purpose

Oral Cavity, Squamous Cell Carcinoma

Status
Completed
Phase
Phase 3
Locations
Taiwan
Study Type
Interventional
Intervention
13-cis Retino Acid
Sponsored by
National Health Research Institutes, Taiwan
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional prevention trial for Oral Cavity

Eligibility Criteria

20 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Clinically free of disease after having undergone surgery for histologically confirmed primary SCC of the oral cavity(Buccal mucosa +Oral tongue ) Without any risk factor of recurrence listed below: Nodal extracapsular spread of disease (ECS) Number of positive node > 2 Perineural involvement Lymphovascular emboli/permeation in resected surgical specimen Histologically positive surgical margins, but no gross residual disease Exclusion Criteria: A KPS of less than 50 percent Serum creatinine and/or GOT/GPT greater than 2 times upper normal limit Distant metastasis Has previously received chemotherapy Has received within the two years diagnosis of any cancer Women of reproductive capacity Cases beyond the age range of 20-65 years.

Sites / Locations

  • National Taiwan University Hospital

Outcomes

Primary Outcome Measures

Primary tumor recurrence

Secondary Outcome Measures

The development of a second primary tumor

Full Information

First Posted
September 13, 2005
Last Updated
September 13, 2005
Sponsor
National Health Research Institutes, Taiwan
Collaborators
National Taiwan University Hospital, Changhua Christian Hospital, China Medical University Hospital, Buddhist Tzu Chi General Hospital, Taichung Veterans General Hospital, Mackay Memorial Hospital, Chang Gung Memorial Hospital, Koo Foundation Sun Yat-Sen Cancer Center, Chi Mei Medical Hospital, National Cheng-Kung University Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT00201279
Brief Title
Chemoprevention Study of Oral Cavity Squamous Cell Carcinoma
Official Title
Phase III Placebo-Controlled Chemoprevention Study of Oral Cavity Squamous Cell Carcinoma Patients
Study Type
Interventional

2. Study Status

Record Verification Date
January 2005
Overall Recruitment Status
Completed
Study Start Date
April 1999 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
September 2012 (undefined)

3. Sponsor/Collaborators

Name of the Sponsor
National Health Research Institutes, Taiwan
Collaborators
National Taiwan University Hospital, Changhua Christian Hospital, China Medical University Hospital, Buddhist Tzu Chi General Hospital, Taichung Veterans General Hospital, Mackay Memorial Hospital, Chang Gung Memorial Hospital, Koo Foundation Sun Yat-Sen Cancer Center, Chi Mei Medical Hospital, National Cheng-Kung University Hospital

4. Oversight

5. Study Description

Brief Summary
The purpose of this study is to study the effect of 13-cis retinoic acid in preventing second primary malignancy in the oral cavity cancer patients after curative local treatment and to study the toxicity and compliance of 13-cis retinoic acid.
Detailed Description
There are more than one thousand deaths annually from head and neck cancer in Taiwan (excluding nasopharyngeal carcinoma) and the majority of treatment failures are related to recurrence of primary disease. Only patients with early-stage disease have high cure rates, but they remain at risk for the development of second primary tumors. Second primary malignancies occur at a constant annual rate of 5% to 7% in all head and neck cancer patients1. Furthermore, because the mortality from primary disease recurrence plateaus after 2 to 3 years in patients with locally advanced disease, second primary tumors become the major cause of late cancer mortality. Sporn et al defined chemoprevention as an effort to arrest or reverse premalignant cells during their progression to invasive malignancy2,3. The concept of chemoprevention has evolved to include the use of specific compounds, rather than general dietary changes, to prevent the development of cancer. Hong et al studied the effects of 13-cis retinoic acid on patients with history of head and neck cancers 4. After treatment of head and neck primary cancers with either radiotherapy or surgery or both, 103 patients were randomized to receive either adjuvant 13-cis retinoic acid or placebo. In an update of this trial with 55 months of follow-up, 16 patients (31%) in the placebo group had developed second primary tumors, whereas 7 patients (14%) in the treatment group had developed second primary tumors (p=0.04) 5. Betel quid chewing becomes increasingly popular in Taiwan. Exposure to both smoking and betel quid significantly increases the risk of oral cavity cancer6. The hazard of developing second primary tumors is high in this population, therefore, chemoprevention is worthy of trial. Use of 13-cis RA for chemoprevention of head and neck cancer only has been published by Hong et al. Their cases included a variety of head and neck cancers that are known to be not a homogenous group. The risk of second primary is different for different primary sites. Therefore, the value of 13-cis RA in chemoprevention is not conclusively addressed. In our proposal, only oral cavity cancer is included and the result will be more convincing. The result could be the basis of further chemoprevention clinical trial or guideline for clinical practice.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Oral Cavity, Squamous Cell Carcinoma

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
Single
Allocation
Randomized
Enrollment
342 (false)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
13-cis Retino Acid
Primary Outcome Measure Information:
Title
Primary tumor recurrence
Secondary Outcome Measure Information:
Title
The development of a second primary tumor

10. Eligibility

Sex
All
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Clinically free of disease after having undergone surgery for histologically confirmed primary SCC of the oral cavity(Buccal mucosa +Oral tongue ) Without any risk factor of recurrence listed below: Nodal extracapsular spread of disease (ECS) Number of positive node > 2 Perineural involvement Lymphovascular emboli/permeation in resected surgical specimen Histologically positive surgical margins, but no gross residual disease Exclusion Criteria: A KPS of less than 50 percent Serum creatinine and/or GOT/GPT greater than 2 times upper normal limit Distant metastasis Has previously received chemotherapy Has received within the two years diagnosis of any cancer Women of reproductive capacity Cases beyond the age range of 20-65 years.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mow-Ming Hsu, MD
Organizational Affiliation
National Taiwan University Hospital
Official's Role
Study Chair
Facility Information:
Facility Name
National Taiwan University Hospital
City
Taipei
ZIP/Postal Code
100
Country
Taiwan

12. IPD Sharing Statement

Links:
URL
http://www.nhri.org.tw
Description
Related Info

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Chemoprevention Study of Oral Cavity Squamous Cell Carcinoma

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