Mutational Profiling in Colorectal Tumors to Determine Its Role in the Diagnosis, Prognostic Significance and Their Impact in Clinical Management

Sponsor
Taipei Medical University WanFang Hospital (Other)
Overall Status
Unknown status
CT.gov ID
NCT01371942
Collaborator
(none)
300
1
36
8.3

Study Details

Study Description

Brief Summary

The aim of this study is to investigate mutational changes occurring in colorectal tumors, from benign polyps, malignant cancer and metastatic tumors. The investigators also plan to establish the clinical correlation, emphasizing on aspects such as the diagnosis and prognosis of disease and the specific treatment outcome. For the purpose, the investigators plan to obtain specimens from patients with colorectal tumors to extract DNA material. The specimens include tissues from either primary (mostly endoscopic biopsies specimens) or metastatic tumors (obtained from sonogram or other imaging modalities guided biopsy), as well as other humors including blood (for serum), malignant ascites, pleural effusions or other body fluids that could be related to CRCs. These patients would receive detailed explanations with regard to the investigations before signing IRB consent. At the initial stage, Wanfang Medical Center would be the only medical institution where endoscopic specimens would be collected. The project would eventually be extended to the Taipei Medical University Hospital and Shuan-Ho Hospital.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    The following are items corresponding to the critical tasks of the project.

    1. Collect, annotate, and store fresh endoscopic specimens of suspicious abnormal tissue (premalignant lesions and primary tumors for genetic mutational investigation;

    2. Collect, annotate, and store fresh specimens from metastatic lesions (e.g.: hepatic metastatic tumors), under sonographic or other imaging modalities guided biopsy procedures;

    3. Collect, process, and store serum, plasma and isolate lymphocytes from blood drawn from patients with colorectal tumor;

    4. Establish a database to link materials acquisition, pathologic, and clinical information on patients who participate in the protocol;

    5. To utilize the clinical database to perform clinical and pathological correlation with the results of current and future scientific studies;

    6. To evaluate genomic and biochemical alterations in colorectal tumors.

    7. To test the effect of small molecule inhibitors on the activation of wild-type and mutant genetic alterations and/or other potential molecular targets.

    8. To correlate tumor genotype and signaling abnormalities with clinical response to genetic alterations and/or other potential molecular targets inhibitors

    9. Analysis of laboratory findings in relationship to patient demographics and clinical course.

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    300 participants
    Official Title:
    Mutational Profiling in Colorectal Tumors to Determine Its Role in the Diagnosis, Prognostic Significance and Their Impact in Clinical Management
    Study Start Date :
    May 1, 2010
    Anticipated Study Completion Date :
    May 1, 2013

    Outcome Measures

    Primary Outcome Measures

      Eligibility Criteria

      Criteria

      Ages Eligible for Study:
      20 Years and Older
      Sexes Eligible for Study:
      All
      Accepts Healthy Volunteers:
      No
      Inclusion Criteria:
      • Patients must have been noted with a colonic tumor (benign polyps or colorectal cancer) on colonoscopy. Patients with lesions located other than the primary tumor (metastatic lesions) such as liver metastasis, enlarged lymph nodes suspicious of metastasis, malignant pleural effusion, ascites, etc. are also enrolled.

      • Age 20

      • Signed consent

      Exclusion Criteria:
      • Known HIV infection

      • Known to have bleeding tendency, precluding for biopsy

      • Any other clinical conditions, which, in the opinion of the principal investigator, would not allow completion of this study

      Contacts and Locations

      Locations

      Site City State Country Postal Code
      1 Taipei Medical University - WanFang Hospital Taipei Taiwan

      Sponsors and Collaborators

      • Taipei Medical University WanFang Hospital

      Investigators

      • Principal Investigator: Gi-Shih Lien, Taipei Medical University WanFang Hospital

      Study Documents (Full-Text)

      None provided.

      More Information

      Publications

      None provided.
      Responsible Party:
      , ,
      ClinicalTrials.gov Identifier:
      NCT01371942
      Other Study ID Numbers:
      • 99064
      First Posted:
      Jun 13, 2011
      Last Update Posted:
      Jun 13, 2011
      Last Verified:
      Jun 1, 2011
      Keywords provided by , ,
      Additional relevant MeSH terms:

      Study Results

      No Results Posted as of Jun 13, 2011