Clinical Trials Directory

Trials / Unknown

UnknownNCT01371942

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

Status
Unknown
Phase
Study type
Observational
Enrollment
300 (estimated)
Sponsor
Taipei Medical University WanFang Hospital · Academic / Other
Sex
All
Age
20 Years
Healthy volunteers
Not accepted

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.

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.

Conditions

Timeline

Start date
2010-05-01
Completion
2013-05-01
First posted
2011-06-13
Last updated
2011-06-13

Locations

1 site across 1 country: Taiwan

Source: ClinicalTrials.gov record NCT01371942. Inclusion in this directory is not an endorsement.