Patients Treated for Chronic Granulomatous Disease (CGD) Since 1995
- Conditions
- Granulomatous Disease, Chronic
- Registration Number
- NCT02082353
- Brief Summary
Chronic granulomatous disease (CGD) is an inherited immune system abnormality in which bone marrow transplantation (BMT) has been shown to be curative. However the risks of transplantation are high and not all patients with CGD may need to undergo this high risk procedure. This study will determine the long term medical condition and daily functioning of participants with CGD after a transplant and if possible, compare these results to participants who do not undergo a transplant.
- Detailed Description
Chronic granulomatous disease (CGD) is an immune deficiency where the neutrophils (a type of white blood cell that kills bacteria and fungi) do no work properly. Some individuals with CGD have neutrophils that do not work at all, whereas others have neutrophils that work partially, but not normally. In the past (over 20 years ago), most individuals with CGD were managed with antibiotics and antifungal medications alone. As the science of blood and marrow transplant (BMT) improved, some with CGD started to receive a BMT. It remained controversial whether individuals with CGD should receive a BMT or medical management alone (antibiotics, antifungals, and other treatments that do not include BMT).
The aim of this natural history study is to better define the role of BMT compared to medical management of CGD. Specifically, what are the outcomes of BMT versus medical management alone, why do some individuals with CGD benefit from BMT, and what are the long-term outcomes of both approaches. Researchers are interested in how individuals with CGD who have no neutrophil function may differ from those with some neutrophil function, how the types of infections and inflammatory complications of CGD impact on survival and how BMT may improve these complications. There are also questions as to how the types of bacteria (called the microbiome) found in the gastrointestinal tract (colon, large intestine) of individuals with CGD influences certain inflammatory complications (such as colitis), and how BMT changes the microbiome in individuals with CGD. All of this will help doctors in the future to better treat patients with CGD.
This study includes a retrospective (looking back into the past), cross-sectional (one time collection of information and/or research testing) and a prospective (looking from today and into the future) component. These are known as longitudinal studies (e.g., looking at information of participants over time).
Persons with CGD who were born 1988 to the present day are eligible, regardless of whether they received a BMT (as long as the BMT was after 1995) or medical therapy only. Individuals who are newly diagnosed with CGD can also be enrolled and followed longitudinally (over time), to determine their outcome from the choice of therapy that is made. An important component of this study is the 'cross sectional' study, where participants with more than 3 years of follow-up after transplant or diagnosis are asked to provide additional research blood work, and information is gathered regarding long-term transplant outcomes such as infections, graft-versus-host disease, autoimmune diseases, and quality of life. In addition, the participants will be asked to provide stool samples to allow investigators to look at how certain bacteria found in the gut (called the microbiome) affect complications of CGD, such as gastrointestinal disease. This will allow primary immune deficiency investigators/doctors to better understand the outcomes of different therapeutic approaches and to best design new treatments and clinical trials in the future for children with CGD.
Recruitment & Eligibility
- Status
- UNKNOWN
- Sex
- All
- Target Recruitment
- 1480
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Participant Inclusion Criteria (Part 1 - Longitudinal Analysis)
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CGD Patients Undergoing Transplant 1995 to Present with Birth Year In or After 1988
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CGD Patients will be Defined by both Defective Neutrophil NADPH Oxidase Function and by Clinical History Consistent with CGD
Patients must have both of:
A functional assay demonstrating abnormal NADPH oxidase function (see A below); AND Clinical history consistent with CGD (see B below).
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Patients must have both "A" and "B":
A. Function: Assays of NADPH Oxidase Function
I. Dihydrorhodamine (DHR) Assay:
- Blood sample was obtained at a time when patient was clinically stable and not critically ill, with control samples performed simultaneously indicating a qualified assay; and
- Assay unequivocally demonstrates CGD with an stimulation index (SI) SI < 35 or equivalent. Assay report, including mean fluorescence intensity (MFI) from unstimulated and stimulated samples and gating strategy, must be de-identified and provided. OR
II. Nitroblue Tetrazolium Oxidation Test (NBT):
o Diagnostic of CGD (reported as reduced granulocyte oxidative response). Report must be de-identified and provided. AND
B. Clinical History: One or More of the Following:
- Severe and/or recurrent infection (liver, perirectal or lung abscess; pneumonia; adenitis; or osteomyelitis) due to, for example, Staphylococcus aureus, Burkholderia sp, Serratia marcescens, non-albicans Candida sp, Aspergillus sp or other mold; or Nocardia sp or other deep tissue infection characteristic of CGD
- Sterile granulomatous disease in respiratory, gastrointestinal or urogenital tracts; or Crohn's disease-like colitis
- A family history consistent with either X-linked or autosomal recessive CGD
In cases where either functional assay (A) or history (B) is equivocal, one or more of the following may be used to confirm a diagnosis of CGD:
C. Absent or significantly reduced in expression or abnormal size of any of the 5 phox components (gp91 phox, p47 phox, p22 phox, p67phox, and p40phox) of NADPH oxidase, by either:
- Western blot
- Northern blot OR D. Mutation in a gene encoding one of the 5 phox components (gp91 phox, p47 phox, p22 phox, p67 phox, and p40 phox) of NADPH oxidase that is predictive of a decreased or absent oxidative burst. (Nonsense, frameshift, or previously described missense mutation associated with CGD).
Molecular Diagnosis is Desirable In addition, molecular diagnosis (gene sequencing and expression analysis) of CGD is desirable and should be performed when possible.
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Further Characterization of Oxidase Level, Longitudinal Study, Prospective Cohort Patients who are to undergo transplantation during the study period must be further characterized as oxidase-null or oxidase positive by level of oxidase production by either:
- DHR assay stimulation Index: where SI ≤ 2.5 will be classified as oxidase-null CGD. Those with SI > 2.5 will be classified as oxidase positive CGD. A single validated test that is accepted by the PID-CGD Review Panel is adequate, but testing on two occasions for validation is desirable. OR
- Ferricytochrome C reduction assay of granulocytes with O2 < 2.3 nmoles /106 cells/h classified as oxidase-null CGD. A single validated test that is accepted by the PID-CGD Review Panel is adequate, but testing on two occasions for validation is desirable.
OR
o Genetic sequencing reporting a mutation that is unequivocally associated to absent oxidase production. (e.g. null mutations) will be classified as oxidase-null CGD (See discussion in Appendix I for how family history, genotype and CGD mutation information will be applied to assigning patients lacking any quantitative oxidase activity measurements to residual oxidase-null or residual oxidase-positive groups).
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Longitudinal Study, Retrospective Cohort Patients who have already been transplanted will be included regardless of whether further characterization by oxidase level (or genotype/mutation data) is possible or not.
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Non-Transplanted CGD Patients with Birth Year In or After 1988 A non-transplant (conventional therapy) group of CGD subjects will be enrolled in the longitudinal study. The non-transplant subjects will be selected from the potentially eligible (retrospective) patient cohort with diagnosis of CGD treated with conventional non-transplant therapy. Participating sites will enter their entire retrospective cohort of CGD patients having birth year in or after 1988 into the registration cohort for this protocol. Baseline for both non-transplant subjects and HCT subjects for the purpose of comparing survival will be the year of birth. However, for non-transplant subjects, many of the detailed analyses such as infection and autoimmune complication rates will be assessed in the year preceding the date of last contact.
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Participant Inclusion Criteria (Part 2 - Cross-Sectional Analysis) To participate in the Cross-Sectional Analysis, patients must have previously been enrolled into the Longitudinal Analysis of Protocol 6903. All transplanted subjects in the Cross-Sectional Analysis are surviving and shall have at least 3 years of follow-up post-transplant to be included. Non-transplanted CGD subjects will become eligible for consideration for the Cross-Sectional Analysis if they were eligible and enrolled in the retrospective cohort of the Longitudinal Analysis, and if/when they are > 3 years post-diagnosis of CGD. Provision of written informed consent will be required for inclusion in the Cross-Sectional Analysis.
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Participant Exclusion Criteria (Longitudinal and Cross- Sectional Analyses)
- Presence of other primary immunodeficiency syndromes that do not meet the clinical and laboratory criteria for CGD.
- Rac2 Deficiency
- Myeloperoxidase Deficiency (MPO Deficiency)
- Glutathione deficiency
- Leukocyte adhesion deficiency syndrome
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Non-transplant subjects:
- The above exclusions pertain.
- In addition, non-transplant subjects will be excluded if the only assessment of oxidase function available is the nitroblue tetrazolium (NBT) test (a non-quantitative test).
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Death HCT to date of death, up to an expected average of 3 years The event analyzed is death from any cause. The time from HCT to death or last follow up will be analyzed. Cause of death will also be collected. Surviving patients will be censored at the time of last observation.
- Secondary Outcome Measures
Name Time Method Quality of Life Measures an expected average of 3 years Age appropriate testing will be performed at the cross-sectional visit in patients surviving at least two years posttransplant:
* Pediatrics quality of life (QL) Family Impact Module, Parent Report
* Peds QL Infant Scales Module (ages 1-24 months), Parent Report
* Peds QL Generic Core Scales for Toddlers (ages 2-4 yr), Parent Report
* Peds QL Generic Core Scales (ages 5-25 yr), Child/Parent Reports
* Peds QL Transplant Module
* Standard Form (SF)-36 (adult)
* Functional Assessment of Cancer Therapy-Bone Marrow Transplant (FACT BMT) (adult)Autoimmune or inflammatory complications an expected average of 3 years - For HCT subjects, inflammation (inflammatory complications) includes chronic graft-versus-host disease (GVHD)
Engraftment an expected average of 3 years Engraftment will be measures in whole blood using either fluorescent in situ hybridization (FISH) for sex chromosomes or short tandem repeat polymerase chain reaction (PCR) or (STRs) in whole blood.
Infections an expected average of 3 years CGD or transplant-related and transplant-related infection
Trial Locations
- Locations (44)
University of Texas Southwestern Medical Center at Dallas
🇺🇸Dallas, Texas, United States
Children's Hospital Los Angeles
🇺🇸Los Angeles, California, United States
UCLA
🇺🇸Los Angeles, California, United States
Children's Healthcare of Atlanta, Emory University
🇺🇸Atlanta, Georgia, United States
Johns Hopkins All Children's Hospital - St. Petersburg, FL
🇺🇸Saint Petersburg, Florida, United States
Alfred I. duPont Hospital for Children/Nemours
🇺🇸Wilmington, Delaware, United States
New York Medical College, Maria Fareri Children's Hospital
🇺🇸Valhalla, New York, United States
Lucile Salter Packard Children's Hospital at Stanford
🇺🇸Palo Alto, California, United States
University of Rochester Medical Center/ Golisano Children's Hospital
🇺🇸Rochester, New York, United States
Children's National Medical Center, Washington DC
🇺🇸Washington, District of Columbia, United States
University of Michigan Health System
🇺🇸Ann Arbor, Michigan, United States
Cardinal Glennon Children's Hospital/ St. Louis University
🇺🇸Saint Louis, Missouri, United States
Children's Hospital of New Orleans at LSUHSC
🇺🇸New Orleans, Louisiana, United States
Nationwide Children's Hospital
🇺🇸Columbus, Ohio, United States
Washington University/ St.Louis Children's Hospital
🇺🇸Saint Louis, Missouri, United States
Memorial Sloan-kettering Cancer Center
🇺🇸New York, New York, United States
Hackensack University Medical Center
🇺🇸Hackensack, New Jersey, United States
The Children's Hospital of Philadelphia
🇺🇸Philadelphia, Pennsylvania, United States
Children's Hospital of Pittsburgh of UPMC
🇺🇸Pittsburgh, Pennsylvania, United States
St. Jude Children's Research Hospital
🇺🇸Memphis, Tennessee, United States
University of Wisconsin/ American Family Children's Hospital
🇺🇸Madison, Wisconsin, United States
Alberta Children's Hospital
🇨🇦Calgary, Alberta, Canada
British Columbia Children's Hospital
🇨🇦Vancouver, British Columbia, Canada
Cancer Care Manitoba
🇨🇦Winnipeg, Manitoba, Canada
The Hospital for Sick Children
🇨🇦Toronto, Ontario, Canada
CHU St. Justine
🇨🇦Montreal, Quebec, Canada
Ann & Robert H. Lurie Children's Hospital of Chicago
🇺🇸Chicago, Illinois, United States
Children's Hospital Boston
🇺🇸Boston, Massachusetts, United States
University of Minnesota Medical Center
🇺🇸Minneapolis, Minnesota, United States
Duke University
🇺🇸Durham, North Carolina, United States
Cincinnati Children's Hospital Medical Center
🇺🇸Cincinnati, Ohio, United States
Rainbow Babies/ University Hospitals Case Medical Center
🇺🇸Cleveland, Ohio, United States
Texas Children's Hospital, Baylor College of Medicine
🇺🇸Houston, Texas, United States
Methodist Children's Hospital of South Texas/Texas Transplant Institute
🇺🇸San Antonio, Texas, United States
Seattle Children's Research Institute
🇺🇸Seattle, Washington, United States
Phoenix Children's Hospital
🇺🇸Phoenix, Arizona, United States
University of Alabama at Birmingham
🇺🇸Birmingham, Alabama, United States
Mayo Clinic Hospital
🇺🇸Rochester, Minnesota, United States
University of California (UCSF) Benioff Children's Hospital
🇺🇸San Francisco, California, United States
Children's Hospital Colorado
🇺🇸Aurora, Colorado, United States
NIH Clinical Center Genetic Immunotherapy Section
🇺🇸Bethesda, Maryland, United States
Oregon Health and Science University
🇺🇸Portland, Oregon, United States
Children's Hospital of Wisconsin-Milwaukee
🇺🇸Milwaukee, Wisconsin, United States
Primary Children's Medical Center/ University of Utah
🇺🇸Salt Lake City, Utah, United States