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Protocol Details

Detection of T cell Somatic Mutations in Bone Marrow Failure Using Whole Exome or Targeted Sequencing

This study is currently recruiting participants.

Summary | Eligibility | Citations | Contacts

Summary

Number

000343-H

Sponsoring Institute

National Heart, Lung and Blood Institute (NHLBI)

Recruitment Detail

Type: Enrolling by Invitation
Gender: Male & Female
Min Age: 18 Years
Max Age: 99 Years

Referral Letter Required

Yes

Population Exclusion(s)

None

Keywords

Myelodysplastic Syndrome;
Natural History

Recruitment Keyword(s)

None

Condition(s)

Bone Marrow Failure;
Myelodysplastic Syndrome

Investigational Drug(s)

None

Investigational Device(s)

None

Intervention(s)

None

Supporting Site

National Heart, Lung, and Blood Institute

Background:

Many immune diseases have gene mutations (changes) in T cells. Bone marrow failure syndromes may also have T cell changes. Researchers want to do whole exome sequencing (WES) on past NIH study participants biospecimens to learn more. They may also do targeted sequencing. WES sequencing will show the exact order of the base pairs in the participant s blood and tissue cells. The results will be linked to the participant s medical records to find out if these changes are associated with how well a person responds to treatment and their overall outcomes.

Objective:

To find out if the development of certain blood diseases is due to gene changes in T cells.

Eligibility:

People with lower risk myelodysplastic syndrome who took part in NIH study 05-H-0206, 09-H-0199, or 04-H-0012.

Design:

Participants will not have study visits. They will be asked to allow their previously collected blood and/or tissue samples to be used. DNA will be taken from their samples for WES. The results of the WES will be linked to their medical records.

Data that can be used to identify participants will be collected. These data include, for example, name, age, and gender. These data will not be used with their samples. Instead, their samples and data will be labeled with a code.

Genes not related to the participant s disease will be reviewed for changes.

Participants will be contacted if certain gene changes are found. They will be asked to give a blood sample. They may have gene counseling.

Participation will end when participants samples have been obtained.

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Eligibility

ELIGIBILITY CRITERIA:

Existing biospecimens and data will be used from research participants with lower risk myelodysplastic syndrome previously enrolled onto protocols 05-H-0206, 09-H-0199, and 04-H-0012


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Citations:

Not Provided

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Contacts:

Principal Investigator

Referral Contact

For more information:

Bhavisha A. Patel, M.D.
National Heart, Lung and Blood Institute (NHLBI)
NIHBC 10 - CRC BG RM 3-5132
10 CENTER DR
BETHESDA MD 20892
(301) 402-3477
bhavisha.patel@nih.gov

Bhavisha A. Patel, M.D.
National Heart, Lung and Blood Institute (NHLBI)
NIHBC 10 - CRC BG RM 3-5132
10 CENTER DR
BETHESDA MD 20892
(301) 402-3477
bhavisha.patel@nih.gov

Office of Patient Recruitment
National Institutes of Health Clinical Center (CC)
Building 61, 10 Cloister Court
Bethesda, Maryland 20892
Toll Free: 1-800-411-1222
Local Phone: 301-451-4383
TTY: TTY Users Dial 7-1-1
ccopr@nih.gov

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