Recruiting

Observational Study

Sponsor:

National Center for Research Resources (NCRR)

Code:

NCT00004342

Conditions

Neutropenia

Eligibility Criteria

Sex: All

Age: 0+

Healthy Volunteers: Not accepted

Study Details

Brief summary:

OBJECTIVES: I. Document the clinical course of severe chronic neutropenia (SCN).

II. Monitor and assess long term safety of primary treatment in SCN patients in the United States, Canada, Europe, and Australia.

III. Study the incidence and outcome of adverse events such as osteoporosis, splenomegaly, cytogenetic abnormalities, myelodysplastic syndrome, and leukemia.

IV. Evaluate growth and development and hematologic parameters. V. Monitor for clinically significant changes in primary treatment response over time.

VI. Establish a physician network to increase the understanding of SCN. VII. Establish a demographic database to allow for future research.

Conditions

Neutropenia

Study ID

NCT00004342

Start date

Jun, 1994

Status verified date

Oct, 2020

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 0+

Healthy Volunteers: Not accepted

Inclusion Criteria - Subjects are eligible for enrollment if they meet the following criteria:

1. A confirmed diagnosis of severe chronic neutropenia based on documented absolute neutrophil counts of less than 0.5x109/L on at least three occasions in the three months prior to enrollment.
2. For subjects with presumed cyclic neutropenia, documentation of at least two neutrophil cycles is preferred. Documentation should include the nadirs with neutrophil counts of less than 200 followed by a clear increase in the counts generally to at least 500 to 1000 followed by a second nadir, usually expected to occur at about three weeks after the first nadir, i.e., cycling with a three week periodicity. Documentation with at least six weeks of counts and two expected nadirs is preferred.

Cases not showing clear oscillations will be categorized as congenital (if neutropenia or neutropenic complications appear to have occurred from birth) or idiopathic (if all symptoms in evidence point to an acquired disorder occurring after the first year of life).
3. Bone marrow aspiration consistent with the diagnosis of congenital, cyclic or idiopathic neutropenia. In all of these conditions, it is expected that the marrow aspirate evaluation at the time of neutropenia will show a deficiency of mature neutrophils. An exception is myelokathexis, a condition with large accumulations of neutrophils with pycnotic nuclei in the marrow. Bone marrow aspirates may show some dyspoiesis of the neutrophil lineage, but abnormalities of erythropoiesis or platelet formation are, in general, inconsistent with the diagnosis of SCN.
4. Normal cytogenetic evaluation. The only exception being cases of well documented severe congenital neutropenia with preferably previously documented normal cytogenetic evaluation will now be enrolled in the Registry at the time of evolution to leukemia.
5. History of recurrent infections (i.e., severe mouth ulcers, gingivitis and sinusitis).
6. Age greater than three months.
7. Independent of hematological parameters, subjects with the following diagnoses may be included: Shwachman-Diamond syndrome (SDS), glycogen storage disease type 1b (GSD1b), Barth syndrome, and Cohen's syndrome.
8. Subjects with moderately severe chronic neutropenia (i.e., ANC less than 1.0x109/L) and recurrent severe infections (i.e., deep tissue infections of subcutaneous areas, lungs, liver, etc.).
9. Immune neutropenia with positive anti-neutrophil antibodies meeting criteria in 1, 3, 5 and 6.
10. All SCN subjects originally enrolled in Amgen-sponsored SCN studies.

Exclusion Criteria

1. Neutropenia known to be drug induced
2. Primary myelodysplasia
3. Primary leukemia
4. Aplastic anemia
5. Known HIV disease
6. Systemic autoimmune diseases such as rheumatoid arthritis or systemic lupus erythematosus
7. Chemotherapy-induced neutropenia (within the last 5 years)

Study Design

Enrollment

1000 participants

Anticipated

Interventions and Outcome Measures

Arms

Adult Neutropenic Subject

Adult subjects with diagnosis of severe chronic neutropenia

Minor Neutropenic Subject

Children under 18 years of age who are diagnosed with severe chronic neutropenia

Parent of Minor Neutropenic Subjects

Parent of minor subjects (i.e., children under 18 years of age) who are diagnosed with severe chronic neutropenia

Central Contacts and Locations

Locations

Dana-Farber/Boston Children¹s Cancer and Blood Disorders Center

Recruiting

Boston, Massachusetts, United States, 02115

Contacts

University of Massachusetts

Recruiting

Worcester, Massachusetts, United States, 01655

Contacts

University of Michigan

Recruiting

Ann Arbor, Michigan, United States, 48109-0266

Contacts

Kelly J. Walkovich, MD

734-647-2893kwalkovi@umich.edu

St. Joseph's Children's Hospital

Recruiting

Paterson, New Jersey, United States, 07503

Contacts

University of Washington School of Medicine

Recruiting

Seattle, Washington, United States, 98195

Contacts

David Chandler Dale

206-543-7215

CancerCare Manitoba

Recruiting

Winnipeg, Manitoba, Canada, R3E 0V9

Contacts

Bonnie Paula Cham

204-787-4147

Hospital for Sick Children

Recruiting

Toronto, Ontario, Canada, M5G 1X8

Contacts

More Information

Sponsor

National Center for Research Resources (NCRR)

Last update posted

Oct 22, 2020

Last verified

Oct, 2020

Keywords

  • chronic neutropenia
  • disease-related problem/condition
  • hematologic disorders
  • neutropenia
  • rare disease
  • severe chronic neutropenia

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by National Center for Research Resources (NCRR) on 2020-10-22.