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Tissue Acquisition and Genomics Analysis of Breast Cancer and Other Gynecologic Malignancies

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ClinicalTrials.gov Identifier: NCT03762733
Recruitment Status : Not yet recruiting
First Posted : December 4, 2018
Last Update Posted : July 19, 2019
Sponsor:
Information provided by (Responsible Party):
National Institutes of Health Clinical Center (CC) ( National Cancer Institute (NCI) )

Tracking Information
First Submitted Date December 1, 2018
First Posted Date December 4, 2018
Last Update Posted Date July 19, 2019
Estimated Study Start Date July 24, 2019
Estimated Primary Completion Date December 29, 2023   (Final data collection date for primary outcome measure)
Current Primary Outcome Measures
 (submitted: December 1, 2018)
Establishment of a tissue repository for the collection and banking of tissue samples [ Time Frame: at study completion ]
A tissue repository
Original Primary Outcome Measures Same as current
Change History Complete list of historical versions of study NCT03762733 on ClinicalTrials.gov Archive Site
Current Secondary Outcome Measures Not Provided
Original Secondary Outcome Measures Not Provided
Current Other Pre-specified Outcome Measures Not Provided
Original Other Pre-specified Outcome Measures Not Provided
 
Descriptive Information
Brief Title Tissue Acquisition and Genomics Analysis of Breast Cancer and Other Gynecologic Malignancies
Official Title Tissue Acquisition and Genomics Analysis of Breast Cancer and Other Gynecologic Malignancies
Brief Summary

Background:

A person s blood, tissue, and other samples contain DNA. Cancer is a disease of cells that are not working properly. It is caused by changes in DNA that build up. Researchers want to do future studies on DNA changes This may help them learn how to guide treatment for cancer. They need biological samples like tumors, blood, and urine for these studies.

Objective:

To create a place to collect and store biological samples from people with gynecologic malignancies like breast cancer. Samples from certain relatives of theirs will be collected too.

Eligibility:

Adults ages 18 and older who are being seen at NIH for breast cancer or other gynecologic malignancy

Their biological relatives of the same age

Design:

Participants will answer questions about their family history.

Participants will have a physical exam and medical history. This will include questions about age, ethnicity, and disease history. They will also answer questions about their medical treatments and responses.

Participants will give blood and urine samples.

Participants may give a tumor tissue sample. This will not be taken specifically for this study. It will be from a previous procedure or one that is already planned.

Other samples may be taken only if a procedure is required for treatment. These include bone marrow, cerebrospinal fluid, and other fluids.

A group of doctors and other professionals will oversee the sample storage place. The group will review all requests to be sure the use of the specimens is valid.

Detailed Description

Background:

  • Increased understanding of the genomic variations of cancer through laboratory evaluations can result in breakthroughs in treatment and improved patient outcomes.
  • Exceptional responders on clinical trials may have mutational characteristics that are unique and unknown, necessitating identification.
  • Current drug development strategies employ precision oncology. This approach identifies molecular targets, with therapies being either chosen or developed to interact with the specific target.
  • The collection and banking of a variety of tissue samples for future translational studies would support research and advance the mission of the NIH.
  • Pleural effusions, ascites as well as other tissues, such as blood, CSF, tumor, bone marrow, and urine, provide a unique opportunity to conduct a variety of translational research, addressing many clinical questions.
  • The establishment of a tissue repository would enhance the mission of the NCI, in helping to advance research supporting precision oncology.

Primary Objective:

-To establish a tissue repository for the collection and banking of tissue samples from patients with breast and/or other gynecologic malignancies, as well as patients consenting 1st -3rd degree biological relatives, seen at the NIH for support of future translational research conducted at the NIH.

Eligibility:

  • Personal diagnosis of breast or other gynecologic malignancy, or be a 1st-3rd degree biological relative of a patient with cancer, currently or previously on a NIH clinical trial.
  • All subjects (index patient with cancer and their 1st-3rd degree biological relatives) must sign consent and enroll onto this study, in order to donate tissue for biobanking on this protocol.
  • Adults, greater than or equal to age 18, willing to provide tissue for biobanking

Design:

  • Samples include, but not limited to tumor (e.g., tissue, outside parrafin blocks or slides), blood, serum, plasma, urine, bone marrow, cerebrospinal fluid (CSF), malignant ascites, and effusions; to be collected after subjects have met eligibility and signed consent. We will also obtain samples (mainly blood) from volunteer, consenting 1st-3rd degree biological relatives of patients with histologically confirmed cancer, to be paired with their family member.
  • The following sample collection strategy is planned, other samples (if applicable) may be collected at the discretion of the PI:

    • Ascites or pleural fluid: approximately 200cc-5L will be collected from patients undergoing therapeutic procedures.
    • Peripheral blood: up to 30ml will be collected via either venipuncture or through existing intravenous access.
    • Tumor tissue: a portion of the cores will be transferred to this study, and tracked via LabMatrix once clinical needs are met on the subject s main treatment protocol, and after subject signs consent. Biopsies will not be performed solely for the purpose of this study.
    • Urine: (5-10 ml) obtained via clean catch method.
    • Bone marrow: (1 core biopsy and half 1 ml of aspirate) obtained via routine sacral biopsy when clinically indicated.
    • CSF: (1-2 ml) obtained via lumbar puncture when clinically indicated.
  • Tissue will be accessed by study investigators. Additional CCR investigators who wish to use tissue from this repository must first provide a written Letter of Intent, (LOI), to be reviewed by an investigator appointed ad hoc committee for approval.
  • Assays used for sample processing, establishment of cell lines, patient derived xenograft models, and storage are described in detail within this protocol. Also, some assays for future translational research are either listed or described herein. Further detailed description of experimental designs, along with statistical analysis, will be provided within future investigator-initiated sample use addendums to this protocol, or new IRB approved protocols, developed in order to study samples from this biorepository.
Study Type Observational
Study Design Observational Model: Cohort
Time Perspective: Prospective
Target Follow-Up Duration Not Provided
Biospecimen Not Provided
Sampling Method Non-Probability Sample
Study Population Patients who are being seen in follow up, consultation, or presenting for enrollment on a clinical trial at the NIH Clinical Center
Condition
  • Breast Cancer
  • Ovarian Cancer
  • Uterine Cancer
Intervention Not Provided
Study Groups/Cohorts
  • Patient Relatives
    Biological relatives (1st-3rd degree) of patients with histologically confirmed malignancy
  • Patients
    Patients with histologically confirmed malignancy
Publications * Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruitment Information
Recruitment Status Not yet recruiting
Estimated Enrollment
 (submitted: December 1, 2018)
500
Original Estimated Enrollment Same as current
Estimated Study Completion Date December 29, 2023
Estimated Primary Completion Date December 29, 2023   (Final data collection date for primary outcome measure)
Eligibility Criteria
  • INCLUSION CRITERIA:
  • Adult subject (age 18 and older)
  • Patient or biological relative of a patient, as follows:

    • Patient with a histologically confirmed breast cancer or other gynecologic malignancy; histopathology of the biopsy tissue must be confirmed by the NCI Laboratory of Pathology, prior to banking of the tissue on this protocol.
    • Biological relative (1st -3rd degree) of a patient who meets the eligibility of histologically confirmed malignancy per above criterion.
  • Subject willingness and ability to provide informed consent.
  • Subject willingness and ability to provide tissue samples for banking.

EXCLUSION CRITERIA:

- Pregnant subjects are eligible to take part; however, sample collection for those who are currently pregnant will only occur as follows:

  • No samples will be drawn for biobanking from a pregnant subject.
  • Primary treatment protocols exclude pregnant patients; therefore, no patient shall be pregnant on this biorepository protocol, while they continue on the treatment protocol; however, once the patient is no longer on the treatment protocol, there is no restriction to pregnancy for this protocol; but, as per the above criterion, no samples will be drawn for biobanking on a pregnant patient.
  • Biological relatives of a patient may not be pregnant at the time of consent and sampling; however, given that this is not a treatment protocol, there is no restriction on pregnancy beyond the time of donation of the samples to be banked (primarily blood for biological relatives)
Sex/Gender
Sexes Eligible for Study: All
Ages 18 Years and older   (Adult, Older Adult)
Accepts Healthy Volunteers No
Contacts
Contact: Rebecca S Trupp, R.N. (240) 760-7533 rebecca.trupp@nih.gov
Listed Location Countries United States
Removed Location Countries  
 
Administrative Information
NCT Number NCT03762733
Other Study ID Numbers 190025
19-C-0025
Has Data Monitoring Committee Not Provided
U.S. FDA-regulated Product Not Provided
IPD Sharing Statement Not Provided
Responsible Party National Institutes of Health Clinical Center (CC) ( National Cancer Institute (NCI) )
Study Sponsor National Cancer Institute (NCI)
Collaborators Not Provided
Investigators
Principal Investigator: Christina M Annunziata, M.D. National Cancer Institute (NCI)
PRS Account National Institutes of Health Clinical Center (CC)
Verification Date June 5, 2019