Gastrointestinal Stromal Tumors (GIST) Registry

Sponsor
M.D. Anderson Cancer Center (Other)
Overall Status
Completed
CT.gov ID
NCT00507273
Collaborator
Novartis Pharmaceuticals (Industry)
1,800
1
64
28.1

Study Details

Study Description

Brief Summary

The goal of this observational research study is to establish a registry of information regarding how different physicians treat and manage patients with gastrointestinal stromal tumors (GISTs).

Objectives:
  1. To describe variation in management of patients with GIST, overall and by patient and provider characteristics.

  2. To provide participating physicians with information regarding management of their patients with GIST compared to the aggregate experience of all physicians participating in the Registry.

Condition or Disease Intervention/Treatment Phase
  • Other: GIST Registry

Detailed Description

The Registry, which is Internet based, is intended to collect information about current practices in the management of GIST without making any specific change to the standard of care as decided by each patient's treating physician.

If you agree to participate in this study, your doctor will provide information to a data registry about your physical and clinical traits, the past and current medical care you have received to treat your GIST, and clinically-related, economically-related, and health-related quality of life information. About 200 doctors will provide information on their patients for the Registry. Your doctor will collect this information when you first join the Registry and at each regularly scheduled visit you make to your doctor's office. The information collection will continue for as long as you and your doctor feel it is appropriate. The information that is entered into the Registry will remain there indefinitely. It is hoped that this sharing of information will lead to a better understanding of how to best treat patients with GIST.

You and your doctor will decide what treatment you will receive. Because this Registry is only to observe actual medical practice, it does not require you to receive any particular treatment.

Only your doctor and people who will help your doctor collect the information for this Registry will know which information submitted to the Registry belongs to you. Data will be tracked in the Registry using only ID numbers and patient initials. The information submitted on the Registry data collection forms will not be associated with a specific patient's identity. Separately, you will be asked to provide your name, place of birth, and Social Security number. This information will not be entered into the Registry databases and will only be used if it is necessary to perform a search should you become lost to follow up. If you do not want to provide your Social Security number you may still be enrolled in the Registry.

This is an investigational study. About 100 patients from M. D. Anderson will be entered into the Registry. In all, about 1800 patients will be registered. The Registry will be active for at least 7 years.

Study Design

Study Type:
Observational
Actual Enrollment :
1800 participants
Observational Model:
Case-Only
Time Perspective:
Prospective
Official Title:
Gastrointestinal Stromal Tumors (GIST) Registry Protocol: reGISTry
Study Start Date :
Aug 1, 2005
Actual Primary Completion Date :
Dec 1, 2010
Actual Study Completion Date :
Dec 1, 2010

Arms and Interventions

Arm Intervention/Treatment
GIST

Patients diagnosed with a gastrointestinal stromal tumor (GIST)

Other: GIST Registry
Internet based data registry about how different physicians treat and manage patients with gastrointestinal stromal tumors.

Outcome Measures

Primary Outcome Measures

  1. Current patterns of medical practice in management of patients with GIS [5 Years]

    Data from observational GIST Registry analyzed to describe current patterns.

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  1. All patients who have been diagnosed with GIST are eligible for enrollment.
Exclusion Criteria:
  1. Patients with a histologic diagnosis other than gastrointestinal stromal tumor (GIST).

Contacts and Locations

Locations

Site City State Country Postal Code
1 UT MD Anderson Cancer Center Houston Texas United States 77030

Sponsors and Collaborators

  • M.D. Anderson Cancer Center
  • Novartis Pharmaceuticals

Investigators

  • Principal Investigator: Jonathon Trent, MD, PhD, M.D. Anderson Cancer Center

Study Documents (Full-Text)

None provided.

More Information

Additional Information:

Publications

None provided.
Responsible Party:
M.D. Anderson Cancer Center
ClinicalTrials.gov Identifier:
NCT00507273
Other Study ID Numbers:
  • 2005-0294
First Posted:
Jul 26, 2007
Last Update Posted:
Aug 2, 2012
Last Verified:
Aug 1, 2012
Keywords provided by M.D. Anderson Cancer Center
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 2, 2012