Full Text View
Tabular View
No Study Results Posted
Related Studies
Analysis of Tumor Tissue and Lymph Nodes Surgically Removed From Patients With Cancers of the Head and Neck
This study is ongoing, but not recruiting participants.
Study NCT00002695   Information provided by National Cancer Institute (NCI)
First Received: November 1, 1999   Last Updated: September 24, 2009   History of Changes

November 1, 1999
September 24, 2009
January 1996
 
 
 
Complete list of historical versions of study NCT00002695 on ClinicalTrials.gov Archive Site
 
 
 
Analysis of Tumor Tissue and Lymph Nodes Surgically Removed From Patients With Cancers of the Head and Neck
CLINICAL EFFICACY OF MOLECULAR ANALYSIS OF SURGICAL MARGINS AND REGIONAL LYMPH NODES IN MANAGEMENT OF HEAD AND NECK SQUAMOUS CELL CARCINOMA

RATIONALE: Diagnostic procedures, such as analysis of tumor tissue and lymph nodes that have been surgically removed, may improve the treatment of patients with cancers of the head and neck.

PURPOSE: Diagnostic trial to determine if analyzing tumor tissue and lymph nodes surgically removed from patients with cancers of the head and neck can predict recurrence of the cancer.

OBJECTIVES:

  • Determine whether molecular detection of p53 mutation in cancerous cells of histologically negative tumor margins can predict local recurrence in patients with squamous cell carcinoma of the upper aerodigestive tract.
  • Determine the incidence of p53 mutation in this population and its correlation with clinical parameters.
  • Determine whether molecular detection of cancerous cells in lymph nodes from stage N0-1 neck dissections can predict survival and the risks of regional recurrence and distant metastases in these patients.

OUTLINE: This is a multicenter study.

Patients undergo standard curative resection and neck node dissection (if appropriate). Specimens are collected from tumor tissue (necrosis-free, if possible), each wound quadrant, any neck disease with clinically negative nodes, and any neck disease with a single positive node for histologic and molecular analysis. Tissue and cells are examined for p53 mutation and DNA microsatellite repeat alterations. Patients undergo adjuvant radiotherapy and/or chemotherapy, as appropriate for clinical staging and histopathology, at the discretion of the participating clinician.

Patients do not receive results of genetic testing and the results do not affect treatment.

Patients are followed every 6 months for 3 years and then annually thereafter.

PROJECTED ACCRUAL: A total 530 patients will be accrued for this study within 3.5 years.

 
Observational
 
Head and Neck Cancer
  • Genetic: DNA stability analysis
  • Genetic: microsatellite instability analysis
  • Genetic: mutation analysis
  • Other: laboratory biomarker analysis
 

*   Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.
 
Active, not recruiting
530
 
 

DISEASE CHARACTERISTICS:

  • Diagnosis of squamous cell carcinoma of the upper aerodigestive tract (excluding the nasopharynx) for which curative resection is scheduled

    • Recurrent disease allowed if resectable
    • Patients with clinically and histologically proven stage N0-1 neck disease who are undergoing dissection are eligible for analysis of occult nodal disease
  • No distant metastasis

PATIENT CHARACTERISTICS:

Age:

  • 18 and over

Performance status:

  • Not specified

Life expectancy:

  • Not specified

Hematopoietic:

  • Not specified

Hepatic:

  • Not specified

Renal:

  • Not specified

Other:

  • No other malignancy within the past 5 years except nonmelanomatous skin cancer or lymphoma

PRIOR CONCURRENT THERAPY:

Biologic therapy:

  • Not specified

Chemotherapy:

  • Prior limited chemotherapy to the index lesion allowed

Endocrine therapy:

  • Not specified

Radiotherapy:

  • Prior limited radiotherapy to the index lesion allowed

Surgery:

  • See Disease Characteristics
  • Prior limited surgery to the index lesion allowed
Both
18 Years and older
No
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT00002695
 
CDR0000064467, E-4393
Eastern Cooperative Oncology Group
National Cancer Institute (NCI)
Study Chair: Wayne M. Koch, MD Sidney Kimmel Comprehensive Cancer Center
National Cancer Institute (NCI)
January 2002

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP