A Study of Lymphangiogenesis in Colorectal and Nasopharyngeal Cancer

Sponsor
National University Hospital, Singapore (Other)
Overall Status
Unknown status
CT.gov ID
NCT00943891
Collaborator
(none)
500
1
77
6.5

Study Details

Study Description

Brief Summary

  1. To determine the association between LVD and clinico-pathologic variables in archived colorectal cancer and Nasopharyngeal carcinoma specimens

  2. To determine the association between VEGF-C,-D expression with COX-2 expression and clinico-pathologic variables in colorectal cancer and Nasopharyngeal carcinoma

  3. To determine the effect of celecoxib on lymphangiogenesis in Nasopharyngeal carcinoma Lymphangiogenesis and factors modulating lymphangiogenesis are associated with clinico-pathological outcome in Nasopharyngeal carcinoma and colorectal cancer. Celecoxib down-regulates lymphangiogenesis Archival colorectal cancer and Nasopharyngeal carcinoma tumor specimens will be obtained from the Department of Pathology. To determine the effect of celecoxib on lymphangiogenesis in Nasopharyngeal carcinoma, the investigators intend to analyze archived specimens collected in a previously conducted study. Colorectal tumor and nodal specimens and Nasopharyngeal carcinoma primary will be examined for MVD, LVD and growth factor expression using established haematoxylin and eosin and immunohistochemical techniques. Quantification of LVD and MVD shall be performed by two pathologists blinded to clinico-pathological variables using standardised methods.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Tumor biopsies

Study Design

Study Type:
Observational
Observational Model:
Case-Crossover
Time Perspective:
Cross-Sectional
Official Title:
A Study of Lymphangiogenesis in Colorectal and Nasopharyngeal Cancer
Study Start Date :
Jul 1, 2008
Anticipated Primary Completion Date :
Dec 1, 2014
Anticipated Study Completion Date :
Dec 1, 2014

Arms and Interventions

Arm Intervention/Treatment
Tumor biopsies

Procedure: Tumor biopsies

Outcome Measures

Primary Outcome Measures

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    21 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Male and female patients are eligible

    • Patients 21 years or older

    Exclusion Criteria:
    • None

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 National University Hospital Singapore Singapore 119074

    Sponsors and Collaborators

    • National University Hospital, Singapore

    Investigators

    • Principal Investigator: Ross Andrew Soo, MBBS, National University Hospital, Singapore

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    , ,
    ClinicalTrials.gov Identifier:
    NCT00943891
    Other Study ID Numbers:
    • MC01/09/08
    First Posted:
    Jul 22, 2009
    Last Update Posted:
    Jan 22, 2014
    Last Verified:
    Jan 1, 2014
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jan 22, 2014