Collecting Tissue Samples From Patients With Cancer Undergoing Radiation Therapy and Healthy Participants

Sponsor
University of Texas Southwestern Medical Center (Other)
Overall Status
Recruiting
CT.gov ID
NCT00992303
Collaborator
(none)
10,000
1
183
54.6

Study Details

Study Description

Brief Summary

RATIONALE: Collecting and storing samples of tissue from patients with cancer to test in the laboratory may help the study of cancer in the future.

PURPOSE: This research study is collecting tissue samples from patients with cancer undergoing radiation therapy. Healthy participants will also be allowed on the trial so their samples can be used in comparison to patients with malignancy

Condition or Disease Intervention/Treatment Phase
  • Other: biologic sample preservation procedure
  • Other: medical chart review
  • Other: questionnaire administration

Detailed Description

OBJECTIVES:

Primary

  • To maintain and create a University of Texas Southwestern Medical Center (UTSW) Radiation Oncology Tissue Resource and Registry/Database that will be used to explore genetic variations contributing to clinical outcomes through tissue analysis and outcome correlation. Tissue will be stored by the UTSTR and the database managed by Radiation Oncology.

Secondary

  • To document disease outcome (local recurrence, distant metastasis, overall survival) by treatment regimen and disease site.

  • To document toxicity by treatment regimen and disease site.

  • To establish a prospective registry/database consisting of patient demographics and outcomes to be used for future research.

OUTLINE: Tissue, including surgical waste, venous blood/serum, urine, bone marrow, and other body fluids, may be collected (at planned surgery and routine medical visits) and preserved for future research. Demographic and disease and treatment information is obtained from patients (by interview or questionnaire), from medical records, and from national datasets. Patients may also be asked to provide additional blood samples and/or a small skin-punch biopsy sample.

Patients are followed up every 6 months for the first two years following treatment and then yearly thereafter.

Study Design

Study Type:
Observational
Anticipated Enrollment :
10000 participants
Observational Model:
Case-Only
Time Perspective:
Cross-Sectional
Official Title:
Tissue Procurement and Outcome Collection for Radiotherapy Treated Patients and Healthy Participants
Study Start Date :
Sep 1, 2009
Anticipated Primary Completion Date :
Dec 1, 2024
Anticipated Study Completion Date :
Dec 1, 2024

Outcome Measures

Primary Outcome Measures

  1. Maintenance a Tissue Resource and Registry/Database [10 years]

    Maintenance and creation of a University of Texas Southwestern Medical Center (UTSW) Radiation Oncology Tissue Resource and Registry/Database

Secondary Outcome Measures

  1. Local recurrence [5 years]

    To document local recurrence by treatment regimen and disease site.

  2. Distant metastasis [5 years]

    To document distant metastasis by treatment regimen and disease site.

  3. Overall survival [5 years]

    To document overall survival by treatment regimen and disease site.

  4. Toxicity by treatment regimen [1 year]

    To document toxicity by treatment regimen and disease site.

  5. Establishment of a prospective registry/database [10 years]

    To establish a prospective registry/database consisting of patient demographics and outcomes to be used for future research.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
DISEASE CHARACTERISTICS:
  • Pathologically-proven diagnosis of malignancy

  • Planning treatment with radiation therapy

PATIENT CHARACTERISTICS:
  • Able to perform follow-up visits

  • Is a patient of the University of Texas Southwestern Medical Center physicians

PRIOR CONCURRENT THERAPY:
  • See Disease Characteristics

  • Participation in other clinical trials is allowed

  • Other prior or concurrent therapy for cancer, such as surgery and/or chemotherapy, is allowed.

Criteria for eligibility:
  • Able to provide written informed consent

  • Age greater than 18 years old

  • Males and Females are eligible

  • Any ethnicity is eligible

Criteria for ineligibility:

-Patients not available for follow-up/future contact

Contacts and Locations

Locations

Site City State Country Postal Code
1 UT Southwestern Medical Center Dallas Texas United States 75390

Sponsors and Collaborators

  • University of Texas Southwestern Medical Center

Investigators

  • Principal Investigator: Puneeth Iyengar, MD, University of Texas Southwestern Medical Center - Dallas

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Puneeth Iyengar, Assistant Professor, University of Texas Southwestern Medical Center
ClinicalTrials.gov Identifier:
NCT00992303
Other Study ID Numbers:
  • STU 072010-098
  • SCCC-032009-049
  • CDR0000653406
First Posted:
Oct 9, 2009
Last Update Posted:
Apr 20, 2022
Last Verified:
Apr 1, 2022
Keywords provided by Puneeth Iyengar, Assistant Professor, University of Texas Southwestern Medical Center

Study Results

No Results Posted as of Apr 20, 2022