Study of Lung Function in Children Who Have Undergone Bone Marrow Transplantation

NCT ID: NCT00009711

Last Updated: 2013-05-01

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

280 participants

Study Classification

OBSERVATIONAL

Study Start Date

1996-03-31

Study Completion Date

2005-08-31

Brief Summary

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RATIONALE: Assessing the long-term effects of bone marrow transplant on lung function in patients may improve the ability to plan treatment.

PURPOSE: This clinical trial studies lung function in pediatric patients who have undergone bone marrow transplant.

Detailed Description

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OBJECTIVES:

* Determine the delayed effects of bone marrow transplantation preparative regimens on pulmonary function in children surviving at least 5 years after transplantation for hematologic malignancy.
* Determine the relationship between pulmonary function and growth rates in these patients.
* Determine the effect of growth hormone treatment on pulmonary function in these patients.
* Determine the relationship between pulmonary function and age at time of transplantation in these patients.
* Determine the incidence and severity of restrictive pulmonary disease, and whether these factors vary with increasing time after transplantation in these patients.

OUTLINE: Patients undergo respiratory history, signs and symptoms assessment, pulmonary function tests (PFT) including spirometry, lung volumes, and diffusion, oxygen saturation by pulse oximetry, and height measurement.

Patients are assessed at 5-10 years, 10-15 years, and over 15 years after bone marrow transplantation. Patients with abnormal PFTs are assessed at more frequent intervals as clinically indicated.

PROJECTED ACCRUAL: Approximately 280 patients will be accrued for this study.

Conditions

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Long-term Effects Secondary to Cancer Therapy in Children Pulmonary Complications

Interventions

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management of therapy complications

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

DISEASE CHARACTERISTICS:

* Patients who have undergone bone marrow transplantation for hematologic malignancy at least 5 years ago

* Disease-free survivors at least 6 years of age AND
* Under 18 years of age at time of transplantation
* Received prior allogeneic, unrelated donor, syngeneic, or autologous bone marrow transplantation
* Able to perform pulmonary function tests

PATIENT CHARACTERISTICS:

Age:

* See Disease Characteristics

Performance status:

* Not specified

Life expectancy:

* Not specified

Hematopoietic:

* Not specified

Hepatic:

* Not specified

Renal:

* Not specified

PRIOR CONCURRENT THERAPY:

Biologic therapy:

* See Disease Characteristics

Chemotherapy:

* Not specified

Endocrine therapy:

* Not specified

Radiotherapy:

* Not specified

Surgery:

* Not specified

Other:

* Any prior preparative regimen allowed
Maximum Eligible Age

17 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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National Cancer Institute (NCI)

NIH

Sponsor Role collaborator

Fred Hutchinson Cancer Center

OTHER

Sponsor Role lead

Principal Investigators

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Jean E. Sanders, MD

Role: STUDY_CHAIR

Fred Hutchinson Cancer Center

Locations

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Fred Hutchinson Cancer Research Center

Seattle, Washington, United States

Site Status

Countries

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United States

Other Identifiers

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FHCRC-1097.00

Identifier Type: -

Identifier Source: secondary_id

NCI-G00-1911

Identifier Type: -

Identifier Source: secondary_id

CDR0000065808

Identifier Type: REGISTRY

Identifier Source: secondary_id

1097.00

Identifier Type: -

Identifier Source: org_study_id

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