Long-Term Follow up of Patients Undergoing Hematopoietic Stem Cell Transplantation

  • STATUS
    Recruiting
  • End date
    Aug 12, 2050
  • participants needed
    2000
  • sponsor
    National Cancer Institute (NCI)
Updated on 28 October 2022
cancer
blood test
allogeneic hematopoietic stem cell transplant
Accepts healthy volunteers

Summary

Background

People who have had an allogeneic hematopoietic stem cell transplant (HCT) have bone marrow or an immune system that is damaged. They get stem cells from a donor who is a relative. Researchers want to study stem cell donors and recipients to learn about the long-term effects of HCT. They want to learn how the stem cells change and how to improve their ability to fight cancer.

Objective

To provide long-term follow-up care for people who underwent or will undergo HCT. To collect data, blood, and tissue samples to learn about late complications after HCT.

Eligibility

Adults age 18 and older who will undergo HCT or underwent HCT and are surviving one year or more from the date of HCT. The stem cell donors for these recipients are also needed.

Design

Recipients will have 1 visit each year. They will have a physical exam. They will answer questions about their medical history and health. They will receive screening and surveillance testing. They will complete brief questionnaires.

Recipients will have blood tests. They may have tissue biopsies or specimens (such as tissue in their cheek or skin or bone marrow biopsy).

Recipients will give their current address and phone number, and the same data for one or two other people, who can get in contact with them.

After the first visit at the clinic, some recipients may see a doctor close to home to get the necessary information and send it to NIH.

Donors will come to the clinic for 1 visit. They will answer questions about their medical history. Blood samples will be taken.

Description

Background
  • Patients who survive more than 3 years after allogeneic hematopoietic stem cell transplantation (HCT) have a high probability of being cured from their underlying disease; however, mortality rates remain 4 to 9-fold higher than the general population for at least 30 years after HCT.
  • The most common causes of late mortality in HCT survivors include second malignancies, relapsed/recurrent disease, infections, chronic graft-versus-host disease (GVHD), respiratory diseases, and cardiovascular diseases.
  • Guidelines for recommended screening and preventive practices for long-term survivors after HCT have been developed, and can be implemented to detect or prevent late complications after HCT.
  • Understanding the pattern of immune reconstitution and immune dysregulation after HCT may help to elucidate the root mechanisms of late complications.
    Objective

-To collect clinical data on patients and late complications after HCT

Eligibility
  • Patients who underwent HCT for any indication and are surviving one year or more from the date of HCT OR patients who will be undergoing HCT on an ETIB protocol.
  • Related stem cell donors of patients meeting the above criteria who participated or will be participating as a donor of stem cells or leukocytes.
  • Age greater than or equal to 4 years
  • Any active disease relapse or new hematologic malignancy including post-transplant lymphoproliferative disorder (PTLD) are excluded from protocol enrollment.
Design
  • Prospective, longitudinal study of the natural history of long-term survivors after HCT.
  • Clinical data on post-transplant complications and peripheral blood samples will be collected at yearly evaluations by the Principal Investigator, LAI, AI or representative investigator of the original HCT protocol.
  • If patient develops complications such as new cancers, relapsed disease, new hematologic malignancy or PTLD they are exempt from required evaluations, and followed for survival and causes of death (management of complications as per primary team).
  • As this is a longitudinal registry study without any planned intervention, there is no formal statistical analysis plan or accrual goal; descriptive data will be reported.

Details
Condition Hematopoietic Stem Cell Transplantation, Tissue Donors
Clinical Study IdentifierNCT03000244
SponsorNational Cancer Institute (NCI)
Last Modified on28 October 2022

Eligibility

Yes No Not Sure

Inclusion Criteria

Related stem cell donors of patients meeting the above criteria as a donor of stem
Age greater than or equal to 4 years
cells or leukocytes
consent document
Ability of patient or patient s Legally Authorized Representative (LAR) to understand
INCLUSION CRITERIA FOR PARENTS COMPLETING SURVEYS
and the willingness to sign a written informed
Parents/guardians of minors enrolled on the study who have undergone HCT
Willingness to complete surveys about the minor that underwent HCT

Exclusion Criteria

Patients with active disease relapse or new hematologic malignancy including
post-transplant lymphoproliferative disorder (PTLD) are excluded from protocol enrollment
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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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