Natural History Study of SCID Disorders

Reticular Dysgenesis Clinical Trial

Official title:

A Prospective Natural History Study of Diagnosis, Treatment and Outcomes of Children With SCID Disorders (RDCRN PIDTC-6901)

Clinical Trial Details — Status: Enrolling by invitation

Administrative data

• NCT number: NCT01186913
• Other study ID #: DAIT RDCRN PIDTC-6901
• Status: Enrolling by invitation
• Start date: September 2, 2010
• Est. completion date: September 2028

Study information

• Verified date: November 2020
• Source: National Institute of Allergy and Infectious Diseases (NIAID)
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

This study is a prospective evaluation of children with Severe Combined Immune Deficiency (SCID) who are treated under a variety of protocols used by participating institutions. In order to determine the patient, recipient and transplant-related variables that are most important in determining outcome, study investigators will uniformly collect pre-, post- and peri-transplant (or other treatment) information on all children enrolled into this study.

Children will be divided into three strata:

• Stratum A: Typical SCID with virtual absence of autologous T cells and poor T cell function

• Stratum B: Atypical SCID (leaky SCID, Omenn syndrome and reticular dysgenesis with limited T cell diversity or number and reduced function), and

• Stratum C: ADA deficient SCID and XSCID patients receiving alternative therapy including PEG-ADA ERT or gene therapy.

Each Group/Cohort Stratum will be analyzed separately.

Description:

This study follows participants with SCID prospectively, meaning the study enrolls participants where there is a plan to receive a blood and marrow transplant, enzyme therapy, or gene therapy in the future. Participants are then followed according to a schedule set out by the study protocol after the procedure. There are no experimental therapies on this study.

The goal of this study is to learn more about: (1) outcomes from the treatment of SCID in the modern era of medicine (2) what factors lead to the best long-term outcomes, such as best donor, conditioning regimen, timing of transplant, etc., and (3) what impact newborn screening and the early diagnosis of SCID has had on the long-term outcomes following BMT or gene therapy. Information is also being gathered on how and when the immune system recovers after bone marrow transplant (BMT), quality of life for long-term survivors, and about whether children develop normally after treatment.

This natural history study is the largest coordinated prospective study of participants with SCID ever performed. Information that investigators will learn, both now and in the future, will help doctors and other health professionals to better treat children with SCID.

Other known NCT identifiers

• NCT02108067

Recruitment information / eligibility

• Status: Enrolling by invitation
• Enrollment: 690
• Est. completion date: September 2028
• Est. primary completion date: September 2028
• Accepts healthy volunteers: No
• Gender: All
• Age group: N/A and older

Eligibility

Inclusion Criteria:

Stratum A: Typical SCID (formerly referred to as Classic SCID)- -Subjects who meet the following inclusion criteria and the intention is to treat with allogeneic hematopoietic cell transplant (HCT) are eligible for enrollment into Stratum A (Typical SCID) of the study:

• Absence or very low number of T cells (CD3 T cells <300/microliter) AND

• No or very low T cell function (<10% of lower limit of normal) as measured by response to phytohemagglutinin (PHA) OR

• T cells of maternal origin present.

Stratum B: Leaky SCID, Omenn Syndrome, Reticular Dysgenesis-

-Subjects who meet the following criteria and the intention is to treat with HCT are eligible for enrollment into Stratum B:

Leaky SCID:

• Maternal lymphocytes tested for and not detected AND

• Either one or both of the following (a,b) :

• a.) <50% of lower limit of normal T cell function as measured by response to PHA, OR response to anti-CD3/CD28 antibody

• b.) Absent or <30% of lower limit of normal proliferative responses to candida and tetanus toxoid antigens

• AND at least two of the following (a through e):

• a.) Reduced number of CD3 T cells

• age =2 years: <1500/microliter

• age >2 years and =4 years: <800/microliter

• age >4 years: <600/microliter

• b.) =80% of CD3+ or CD4+ T cells that are CD45RO+

• AND/OR >80% of CD3+ or CD4+ T cells are CD62L negative

• AND/OR >50% of CD3+ or CD4+T cells express HLA-DR (at <4 years of age)

• AND/OR are oligoclonal T cells

• c.) Hypomorphic mutation in IL2RG in a male, or homozygous hypomorphic mutation or compound heterozygosity with =1 hypomorphic mutation in an autosomal SCID-causing gene

• d.) Low T Cell Receptor Excision Circles (TRECs) and/or the percentage of CD4+/45RA+/CD31+ or CD4+/45RA+/CD62L+ cells is below the lower limit of normal.

• e.) Functional testing in vitro supporting impaired, but not absent, activity of the mutant protein, AND

• Does not meet criteria for Omenn Syndrome.

Omenn Syndrome:

• Generalized skin rash

• Maternal lymphocytes tested for and not detected;

--Note: If maternal engraftment was not assessed and ruled out, the subject is not eligible as Omenn Syndrome.

• =80% of CD3+ or CD4+ T cells are CD45RO+ AND/OR

• 80% of CD3+ or CD4+T cells are CD62L negative AND/OR

• 50% of CD3+ or CD4+ T cells express HLA-DR (at <2 years of age);

• Absent or low (< 30% lower limit of normal) T cell proliferation response to antigens (Candida, tetanus) to which the subject has been exposed

NOTE: If proliferation to antigen was not performed, but at least 4 of the following 9 supportive criteria, at least one of which must be among those marked with an asterisk (*) below are present, the subject is eligible as Omenn Syndrome:

• Hepatomegaly

• Splenomegaly

• Lymphadenopathy

• Elevated IgE

• Elevated absolute eosinophil count

• *Oligoclonal T cells measured by CDR3 length or flow cytometry

• *Proliferation to PHA is reduced <50% of lower limit of normal or SI <30

• *Hypomorphic mutation in a SCID causing gene

• Low TRECS and/or the percentage of CD4+/45RA+/CD31+ or CD4+/45RA+/CD62L+ cells is below the lower limit of normal.

Reticular Dysgenesis:

• Absence or very low number of T cells (CD3 <300/µL

• No or very low (<10% lower limit of normal) T cell response to PHA

• Severe neutropenia (absolute neutrophil count < 200 /µL) AND

• =2 of the following (a,b,c):

• a.) Sensori-neural deafness

• b.) Deficiency of marrow granulopoiesis on bone marrow examination

• c.) A pathogenic mutation in the adenylate kinase 2 (AK2) gene identified.

Stratum C:

Subjects who meet the following criteria and the intention is to treat with therapy other than allogeneic HCT, primarily PEG-ADA ERT or gene therapy with autologous modified (gene transduced) cells, are eligible for enrollment into

Stratum C:

• ADA Deficient SCID with intention to treat with PEG-ADA ERT

• ADA Deficient SCID with intention to treat with gene therapy

• X-linked SCID with intention to treat with gene therapy

• Any SCID patient previously treated with a thymus transplant (includes intention to treat with HCT, as well as PEG-ADA ERT or gene therapy)

• Any SCID patient who received therapy for SCID deemed "non-standard" or "investigational", including in utero procedures.

Exclusion Criteria:

-Subjects who meet any of the following exclusion criteria are disqualified from enrollment in Strata A, B, or C of the study:

• Presence of an Human Immunodeficiency Virus (HIV) infection (by PCR) or other cause of secondary immunodeficiency

• Presence of DiGeorge syndrome

• MHC Class I and MHC Class II antigen deficiency, and

• Metabolic conditions that imitate SCID or related disorders such as folate transporter deficiency, severe zinc deficiency or transcobalamin deficiency.

Related Conditions & MeSH terms

• ADA SCID
• Immunologic Deficiency Syndromes
• Leaky SCID
• Omenn Syndrome
• Reticular Dysgenesis
• Severe Combined Immunodeficiency
• Severe Combined Immunodeficiency (SCID)
• XSCID

Locations

Country	Name	City	State
Canada	Alberta Children's Hospital	Calgary	Alberta
Canada	CHU Sainte-Justine	Montreal	Quebec
Canada	The Hospital for Sick Children	Toronto	Ontario
Canada	British Columbia Children's Hospital	Vancouver	British Columbia
Canada	Cancer Care Manitoba	Winnipeg	Manitoba
United States	University of Michigan Health System	Ann Arbor	Michigan
United States	Children's Healthcare of Atlanta/Emory University School of Medicine	Atlanta	Georgia
United States	NIH Clinical Center Genetic Immunotherapy Section	Bethesda	Maryland
United States	University of Alabama at Birmingham	Birmingham	Alabama
United States	Children's Hospital Boston	Boston	Massachusetts
United States	Ann & Robert H. Lurie Children's Hospital of Chicago	Chicago	Illinois
United States	Cincinnati Children's Hospital Medical Center	Cincinnati	Ohio
United States	University Hospitals-Rainbow Babies and Children's Hospital	Cleveland	Ohio
United States	Nationwide Children's Hospital	Columbus	Ohio
United States	University of Texas Southwestern Medical Center/Children's of Dallas	Dallas	Texas
United States	Children's Hospital Denver	Denver	Colorado
United States	Duke University	Durham	North Carolina
United States	Hackensack University Medical Center	Hackensack	New Jersey
United States	Texas Children's Hospital	Houston	Texas
United States	Children's Hospital Los Angeles	Los Angeles	California
United States	University of California, Los Angeles	Los Angeles	California
United States	University of Wisconsin/ American Family Children's Hospital	Madison	Wisconsin
United States	St. Jude Children's Research Hospital	Memphis	Tennessee
United States	Medical College of Wisconsin	Milwaukee	Wisconsin
United States	University of Minnesota Medical Center	Minneapolis	Minnesota
United States	Children's Hospital/Louisiana State University Health Sciences Center	New Orleans	Louisiana
United States	Memorial Sloan-Kettering Cancer Center	New York	New York
United States	Lucile Salter Packard Children's Hospital at Stanford	Palo Alto	California
United States	The Children's Hospital of Philadelphia	Philadelphia	Pennsylvania
United States	Phoenix Children's Hospital	Phoenix	Arizona
United States	Children's Hospital of Pittsburgh of UPMC	Pittsburgh	Pennsylvania
United States	Oregon Health and Science University	Portland	Oregon
United States	Mayo Clinic Hospital	Rochester	Minnesota
United States	University of Rochester Medical Center/ Golisano Children's Hospital	Rochester	New York
United States	Cardinal Glennon Children's Medical Center	Saint Louis	Missouri
United States	Washington University St Louis Children's Hospital	Saint Louis	Missouri
United States	Johns Hopkins All Children's Hospital	Saint Petersburg	Florida
United States	Primary Children's Medical Center/University of Utah	Salt Lake City	Utah
United States	Methodist Children's Hospital of South Texas/Texas Transplant Institute	San Antonio	Texas
United States	University of California San Francisco Children's Hospital	San Francisco	California
United States	Seattle Children's Research Institute	Seattle	Washington
United States	New York Medical College, Maria Fareri Children's Hospital	Valhalla	New York
United States	Children's National Medical Center	Washington	District of Columbia
United States	Alfred I. duPont Hospital for Children/Nemours	Wilmington	Delaware

Sponsors (4)

Lead Sponsor	Collaborator
National Institute of Allergy and Infectious Diseases (NIAID)	National Center for Advancing Translational Science (NCATS), Office of Rare Diseases (ORD), Primary Immune Deficiency Treatment Consortium (PIDTC)

Countries where clinical trial is conducted

United States,  Canada, 

References & Publications (9)

Dvorak CC, Cowan MJ, Logan BR, Notarangelo LD, Griffith LM, Puck JM, Kohn DB, Shearer WT, O'Reilly RJ, Fleisher TA, Pai SY, Hanson IC, Pulsipher MA, Fuleihan R, Filipovich A, Goldman F, Kapoor N, Small T, Smith A, Chan KW, Cuvelier G, Heimall J, Knutsen A — View Citation

Dvorak CC, Haddad E, Buckley RH, Cowan MJ, Logan B, Griffith LM, Kohn DB, Pai SY, Notarangelo L, Shearer W, Prockop S, Kapoor N, Heimall J, Chaudhury S, Shyr D, Chandra S, Cuvelier G, Moore T, Shenoy S, Goldman F, Smith AR, Sunkersett G, Vander Lugt M, Ca — View Citation

Griffith LM, Cowan MJ, Kohn DB, Notarangelo LD, Puck JM, Schultz KR, Buckley RH, Eapen M, Kamani NR, O'Reilly RJ, Parkman R, Roifman CM, Sullivan KE, Filipovich AH, Fleisher TA, Shearer WT. Allogeneic hematopoietic cell transplantation for primary immune deficiency diseases: current status and critical needs. J Allergy Clin Immunol. 2008 Dec;122(6):1087-96. doi: 10.1016/j.jaci.2008.09.045. Epub 2008 Nov 6. — View Citation

Griffith LM, Cowan MJ, Notarangelo LD, Kohn DB, Puck JM, Pai SY, Ballard B, Bauer SC, Bleesing JJ, Boyle M, Brower A, Buckley RH, van der Burg M, Burroughs LM, Candotti F, Cant AJ, Chatila T, Cunningham-Rundles C, Dinauer MC, Dvorak CC, Filipovich AH, Fle — View Citation

Griffith LM, Cowan MJ, Notarangelo LD, Kohn DB, Puck JM, Shearer WT, Burroughs LM, Torgerson TR, Decaluwe H, Haddad E; workshop participants. Primary Immune Deficiency Treatment Consortium (PIDTC) update. J Allergy Clin Immunol. 2016 Aug;138(2):375-85. do — View Citation

Griffith LM, Cowan MJ, Notarangelo LD, Puck JM, Buckley RH, Candotti F, Conley ME, Fleisher TA, Gaspar HB, Kohn DB, Ochs HD, O'Reilly RJ, Rizzo JD, Roifman CM, Small TN, Shearer WT; Workshop Participants. Improving cellular therapy for primary immune defi — View Citation

Haddad E, Allakhverdi Z, Griffith LM, Cowan MJ, Notarangelo LD. Survey on retransplantation criteria for patients with severe combined immunodeficiency. J Allergy Clin Immunol. 2014 Feb;133(2):597-9. doi: 10.1016/j.jaci.2013.10.022. Epub 2013 Dec 10. — View Citation

Pai SY, Logan BR, Griffith LM, Buckley RH, Parrott RE, Dvorak CC, Kapoor N, Hanson IC, Filipovich AH, Jyonouchi S, Sullivan KE, Small TN, Burroughs L, Skoda-Smith S, Haight AE, Grizzle A, Pulsipher MA, Chan KW, Fuleihan RL, Haddad E, Loechelt B, Aquino VM — View Citation

Shearer WT, Dunn E, Notarangelo LD, Dvorak CC, Puck JM, Logan BR, Griffith LM, Kohn DB, O'Reilly RJ, Fleisher TA, Pai SY, Martinez CA, Buckley RH, Cowan MJ. Establishing diagnostic criteria for severe combined immunodeficiency disease (SCID), leaky SCID, — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Overall Survival (OS) at Month 6 Post HCT	Assess the overall survival (OS) for participants after hematopoietic stem cell transplantation (HCT) for treatment of Severe Combined Immunodeficiency (SCID).; The time to this event is the time from HCT to death or last follow-up (whichever occurs first). All participants will be followed for a minimum of 6 months from HCT. Overall survival will be estimated at 6 months.	Month 6 Post HCT
Primary	Overall Survival (OS) at Year 2 Post HCT	Assess the overall survival (OS) for participants after hematopoietic stem cell transplantation (HCT) for treatment of Severe Combined Immunodeficiency (SCID).; The time to this event is the time from HCT to death or last follow-up (whichever occurs first). All participants will be followed for a minimum of 6 months from HCT. Overall survival will be estimated at 2 years.	Year 2 Post HCT
Primary	Overall Survival (OS) at Year 5 Post HCT	Assess the overall survival (OS) for participants after hematopoietic stem cell transplantation (HCT) for treatment of Severe Combined Immunodeficiency (SCID).; The time to this event is the time from HCT to death or last follow-up (whichever occurs first). All participants will be followed for a minimum of 6 months from HCT. Overall survival will be estimated at 5 years.	Year 5 Post HCT
Primary	Overall Survival (OS) at Year 8 Post HCT	Assess the overall survival (OS) for participants after hematopoietic stem cell transplantation (HCT) for treatment of Severe Combined Immunodeficiency (SCID).; The time to this event is the time from HCT to death or last follow-up (whichever occurs first). All participants will be followed for a minimum of 6 months from HCT. Overall survival will be estimated at 8 years.	Year 8 Post HCT
Secondary	T Cell Reconstitution by Stratum-Month 6, Year 2, Year 5 and Year 8 Post-SCID Treatment	A measure of immune reconstitution defined by the presence of three out of four of: Lymphocyte proliferation to PHA =50% of lower limit of normal control; Total CD3+ > 1000 / microliter; Total CD4+ > 500 / microliter; Total CD4+ CD45RA+ > 200 / microliter; AND, for participants who received allogeneic HCT: -Donor T cell chimerism =80%	From SCID Treatment (HCT, ERT or GT) to Month 6, Year 2, Year 5 and Year 8 Post-SCID Treatment
Secondary	B Cell Reconstitution by Stratum-Month 6, Year 2, Year 5 and Year 8 Post-SCID Treatment	A measure of immune reconstitution defined by: -Intravenous Immunoglobulin (IVIG) independence and at least three of the following: Normal IgA and IgM levels for age; Normal IgG levels for age, independent of supplemental gammaglobulin; Isohemagglutinins =1:8; Specific antibody production while off IVIG	From SCID Treatment (HCT, ERT or GT) to Month 6, Year 2, Year 5 and Year 8 Post-SCID Treatment
Secondary	Engraftment at Day 100, Month 6, Year 2, Year 5 and Year 8 Post-HCT	Whole-blood engraftment and engraftment in T-, B-, or Natural Killer (NK)-cell subsets will be assessed.; For whole blood and subsets*, the following engraftment criteria will be used: < 5% donor = autologous reconstitution; 5-80% donor = mixed chimerism; = 80% donor = full chimerism; Subsets: CD3; CD19; CD14 and/or CD15 (myeloid cells); CD3- CD56+ NK cells; Outcome analysis restricted to participants with hematopoietic (stem) cell transplantation (HCT) intervention.	From HCT to Month 6, Year 2, Year 5 and Year 8 Post-HCT
Secondary	Time to Resolution of Infections Diagnosed Prior to HCT	Time to resolution of any "pre-HCT" infections-bacterial, viral or fungal. Participants who are alive without resolving their pre-HCT infections will be considered censored at last contact.; Resolution of pre-existing infection defined by: Participant being clinically well,; Participant off treatment for infection(s), and/or; Negative culture/PCR assay.; Outcome analysis restricted to participants with pre-hematopoietic (stem) cell transplantation (HCT) opportunistic infections.	Through study completion, up to 8 years post-HCT
Secondary	Incidence of New Infections Post-HCT	The occurrence of new documented bacterial, viral, or fungal infections-by site of disease, organism, date of onset, and resolution- post-HCT.; Participants who are alive without infection will be considered censored at last contact.; Outcome analysis restricted to participants with hematopoietic (stem) cell transplantation (HCT).	From HCT to Day 100, Month 6, Year 1, Year 2, Year 5, and Year 8 post-HCT
Secondary	Proportion of Participants Achieving Normal Nutritional Status Post-HCT	Normal nutrition status defined by: Absence of chronic diarrhea and/or; No longer requiring supplemental nutrition (i.e., tube feeding or TPN).; TPN: total parenteral nutrition; Outcome analysis restricted to participants with hematopoietic (stem) cell transplantation (HCT) intervention.	Baseline (Pre-HCT) to Year 1, Year 2, Year 5 and Year 8 Post-HCT
Secondary	Longitudinal Analysis: Growth Percentile in Body Height	Participant's height will be superimposed against gender specific standard growth charts.	Baseline (Pre-HCT), Year 1, Year 2, Year 5 and Year 8 Post-HCT
Secondary	Longitudinal Analysis: Growth Percentile in Body Weight	Participant's weight will be superimposed against gender specific standard growth charts.	Baseline (Pre-HCT), Year 1, Year 2, Year 5 and Year 8 Post-HCT
Secondary	Incidence of Acute Graft Versus Host Disease (GVHD) Post-HCT	Occurrence of acute GVHD. Any skin, gastrointestinal or liver abnormalities fulfilling the consensus criteria of Grades II-IV acute GVHD or grades III-IV acute GVHD are considered events.; Participants alive without acute GVHD will be censored at the time of last follow-up.; Outcome analysis restricted to participants with hematopoietic (stem) cell transplantation (HCT) intervention.	From HCT to Day 100 and Month 6 post-HCT
Secondary	Incidence of Chronic Graft Versus Host Disease (GVHD) Post-HCT	Occurrence of chronic GVHD in any organ system fulfilling the criteria of limited or extensive chronic GVHD. Participants alive without chronic GVHD will be censored at time of last follow-up.; Outcome analysis restricted to participants with hematopoietic (stem) cell transplantation (HCT).	From HCT to Month 6, Year 1,Year 2, Year 5 and Year 8 Post-HCT
Secondary	Incidence of Autoimmunity Requiring Treatment by Stratum- Month 6, Year 2, Year 5 and Year 8 Post-SCID Treatment	Occurrence of autoimmunity requiring treatment with immunosuppression or other therapy. Participants alive without autoimmunity will be censored at time of last follow-up.; Date of onset and type of treatment will be collected on: Autoimmune hypothyroidism; Autoimmune cytopenia (hemolytic anemia, thrombocytopenia, neutropenia); Arthritis; Myositis; Nephritis; Bronchiolitis obliterans or other pulmonary autoimmune disease; Vitiligo; Alopecia; Inflammatory bowel disease; Neurodegeneration; Vasculitis	From SCID Treatment (HCT, ERT or GT) to Month 6, Year 2, Year 5 and Year 8 Post-SCID Treatment
Secondary	Infant Neurocognitive Development By Stratum Measured by Bayley's Scales for Infant Development 3rd edition (BSID-III-R)	Infant development as measured by Bayley's scales for infant development 3rd edition (BSID-III-R, Bayley, 2006).] The BSID III-R is a standardized developmental exam that is normalized to the age of the child in months. The mean adjusted score is 100 with a standard deviation of 15 (higher being better). Evaluation conducted as per standard of care in participants =30 months of age.	Baseline (Pre-SCID Treatment-HCT, ERT or GT),Year 1, Year 2, Year 4, Year 5 and Year 8 Post-SCID Treatment
Secondary	Neurocognitive Development By Stratum Measured by Vineland Adaptive Behavior Scales, Second Edition (Vineland II)	The Vineland II measures the personal and social skills of individuals from birth through adulthood. Since adaptive behavior refers to an individual's typical performance of the day-to-day activities required for personal and social sufficiency, these scales assess what a person actually does, rather than what he or she is able to do.; Summary: The Vineland II is a measure of adaptive behavior in children, adolescents and adults. It yields an overall standard score (Adaptive Behavior Composite, ABC) and age standard scores in four domains: Communication, Daily Living Skills, Motor Skills, and Maladaptive Behaviour Index.; ABC scores have a mean of 100 and a standard deviation of 15 (range = 20 to 160). Higher scores suggest a higher level of adaptive functioning. A rise in standard scores from Baseline indicates improvement.; Evaluation as per standard of care.	Baseline (Pre-SCID Treatment-HCT, ERT or GT),Year 1, Year 2, Year 4, Year 5 and Year 8 Post-SCID Treatment
Secondary	Neurocognitive Development By Stratum Measured by Wechsler Preschool and Primary Intelligence Scale of Intelligence, Third Edition (WPPSI III)	Cognitive ability assessed using the WPPSI III. The WPPSI-III has been developed and standardized for children ages 2 years, 6 months through 7 years, 3 months of age. The WPPSI-III yields a Verbal Score, a Performance Score, a General Language Score, and a Full Scale Score. These scores have a mean of 100 and a standard deviation of 15. The range of possible values is 50 (worst value) to 150 (best value).; Evaluation as per standard of care.	Baseline (Pre-SCID Treatment-HCT, ERT or GT),Year 1, Year 2, Year 4, Year 5 and Year 8 Post-SCID Treatment
Secondary	Neurocognitive Assessment by Stratum Using the Wechsler Intelligence Scale for Children, Fourth Edition (WISC-IV)	The WISC-IV is designed for children 6 years 0 months to 16 years 11 months. The Full Scale IQ, ranges from 45 to 155 with a mean of 100 and standard deviation of 15. Higher scores indicate stronger cognitive function. Scores between 90 and 110 are considered to be within the range of average IQ. Evaluation in accordance with standard of care, participant ages 6 years and above.	Baseline (Pre-SCID Treatment-HCT, ERT or GT),Year 1, Year 2, Year 4, Year 5 and Year 8 Post-SCID Treatment
Secondary	Incidence of Complications of HCT Requiring Treatment	Occurrence of health event(s) classified as an HCT treatment complication, including but not limited to: Veno-occlusive disease; Thrombotic thrombocytopenic purpura; Bronchiolitis obliterans / chronic lung disease; Seizures; Hypertension; Outcome analysis restricted to participants with hematopoietic (stem) cell transplantation (HCT) intervention.	From HCT to Month 6, Year 1,Year 2, Year 5 and Year 8 Post-HCT
Secondary	Comparison of Quality of Life (QOL) By Stratum Prior to and After SCID Treatment: Scores for Pediatric Quality of Life Questionnaire (Peds-QL)	The Peds-QL is a generic Health-Related Quality of Life (HR QoL) instrument designed specifically for a pediatric population. It captures the following domains: general health/activities, feelings/emotional, social functioning, school functioning. Higher scores indicate better quality of life (QOL) for all domains of the Peds-QL. This modular instrument uses a 5-point scale: from 0 (never) to 4 (almost always). Items are reversed scored and linearly transformed to a 0-100 scale as follows: 0=100, 1=75, 2=50, 3=25, 4=0. 4 dimensions (physical, emotional, social, & school functioning) are scored.	Baseline (Pre-SCID Treatment-HCT, ERT or GT) to Year 1, Year 2, Year 4, Year 5 and Year 8 Post-SCID Treatment

External Links

•   Division of Allergy, Immunology, and Transplantation (DAIT)
•   National Center for Advancing Translational Science (NCATS)
•   National Institute of Allergy and Infectious Diseases (NIAID)
•   Primary Immune Deficiency Treatment Consortium (PIDTC) featured highlights
•   Rare Diseases Clinical Research Network (RDCRN)