Retrospective Study of Viral Reactivation Across All Bone Marrow Transplant Protocols Since 2010

Sponsor
National Cancer Institute (NCI) (NIH)
Overall Status
Completed
CT.gov ID
NCT03111745
Collaborator
(none)
730
1
34.2
21.3

Study Details

Study Description

Brief Summary

Background:

Some blood and immune disorders can be helped with HSCT. This is allogeneic hematopoietic stem cell transplantation. The person who gets the stem cells has their immune system suppressed. This is done to help prevent their body from rejecting the transplant. During this time, the person is at a high risk to get viral infections. Researchers want to study the records of people who had transplants a few years ago. They want to look at how often certain viral complications happened.

Objective:

To study how often certain viral complications occurred after HSCT and what risks factors were involved.

Eligibility:

Records will be reviewed. No participants will be contacted.

Design:

Researchers will review medical records from the NIH Clinical Center.

The records will be from people who had HSCT between 2010 and 2015 when they were between 4 and 85 years old. They already gave consent for their data to be studied.

Data collected will include:

Vital statistics like age and sex

Viral status of the recipient and donor

Reason for transplant

Transplant details

How the immune system recovered after transplant

If the recipient got graft versus host disease

Any infections

Overall survival

...

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    This protocol is a retrospective chart review of patients who have underwent hematopoietic stem cell transplantation (HSCT) at the NIH Clinical Center. If this proposal is approved, BTRIS will identify and populate the patients in these protocols, and BTRIS identified reports will be used going forward.

    BTRIS identified reports will be used to review patient progress notes, all aspects of the transplant platform, as well as viral titers over the course of each patient s follow-up, supplemented by review of paper or CRIS electronic medical records as needed.

    The study will involve review of patient records and will not use specimens or participant contact. The participants whose records will be reviewed in this protocol were enrolled in NIH protocols between 2010 and December 1, 2020. BTRIS policy requires approval from Principal Investigators on certain protocols. These Principal Investigators have been contacted via email for permission to conduct this study and have verified that none of the original protocols or informed consent documents precludes such a review of clinical data.

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    730 participants
    Observational Model:
    Cohort
    Time Perspective:
    Retrospective
    Official Title:
    Retrospective Study of Viral Reactivation Across All Bone Marrow Transplant Protocols Since 2010
    Actual Study Start Date :
    Apr 13, 2017
    Actual Primary Completion Date :
    Dec 29, 2018
    Actual Study Completion Date :
    Feb 18, 2020

    Arms and Interventions

    Arm Intervention/Treatment
    1

    Retrospective chart review of patients who have underwent hematopoietic stem celltransplantation (HSCT)

    Outcome Measures

    Primary Outcome Measures

    1. To determine the incidence and risk factors for various viral complications by HSCT platform and its relation to immune reconstitution. [1 year]

      Incidence and risk factors for various viral complications by HSCT platform and its relation to immune reconstitution.

    Secondary Outcome Measures

    1. Evaluate the relationship between EBV and CMV in blood [1 year]

      Evaluate the relationship between EBV and CMV in blood

    2. incidence of late CMV, EBV, BK cystitis, adenovirus, HHV6 encephalitis, JC virus, and CNS disease [1 year]

      incidence of late CMV, EBV, BK cystitis, adenovirus, HHV6 encephalitis, JC virus, and CNS disease

    3. evaluate relationship between viral infection and immunologic parameters [1 year]

      evaluate relationship between viral infection and immunologic parameters

    4. evaluate relationship between GVHD and viral infection incidence/burden [1 year]

      evaluate relationship between GVHD and viral infection incidence/burden

    5. determine overall survival and incidence of infection- relatedmortality [1 year]

      determine overall survival and incidence of infection- relatedmortality

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    4 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    • ELIGIBILITY CRITERIA:

    Subjects will not be recruited for this study.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 National Cancer Institute (NCI) Bethesda Maryland United States 20892

    Sponsors and Collaborators

    • National Cancer Institute (NCI)

    Investigators

    • Principal Investigator: Jennifer A Kanakry, M.D., National Cancer Institute (NCI)

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    National Cancer Institute (NCI)
    ClinicalTrials.gov Identifier:
    NCT03111745
    Other Study ID Numbers:
    • 999917079
    • 17-C-N079
    First Posted:
    Apr 13, 2017
    Last Update Posted:
    Aug 25, 2022
    Last Verified:
    Dec 6, 2021
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by National Cancer Institute (NCI)
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Aug 25, 2022