Chronic Lymphocytic Leukemia Clinical Trial

Osteoporosis in Children With ALL

Summary

Hypothesis:

Pediatric patients with acute lymphoblastic leukemia, treated with chronic glucocorticoids as a part of the leukemia treatment protocol, will have an increased incidence and severity of osteoporosis.

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Full Description

Osteoporosis is a disease characterized by low bone mass and microarchitectural deterioration of bone tissue. Osteoporosis is a devastating disorder with significant physical, psychosocial and financial consequences. Intensive chemotherapy and radiotherapy have led to significant improvements in long term, disease-free survival of children with malignancies. Unfortunately, there are many deleterious side effects associated with this therapy. Little is known about the longitudinal changes in bone mass accumulation and bone metabolism in these patients.

The purpose of this study is to evaluate the timing and severity of changes in bone mineral metabolism for children treated for childhood leukemia. Data will be used to establish treatment protocols with the goal of preventing severe fractures and pain in the acute treatment stage and severe osteoporosis and related pathology in the chronic stage.

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Eligibility Criteria

Inclusion Criteria:

All pediatric patients with a new diagnosis of ALL between ages 4-18
Patients who are expected to receive glucocorticoids as part of the leukemia treatment protocol
Bone density measurements must be performed at the diagnosis visit or maximally within 48 hours after the first dose of glucocorticoids

Exclusion Criteria:

Patients under 4 years of age are excluded due to lack of age appropriate standards for bone mineral density
Glucocorticoid therapy of at least one month or longer within the six months prior to DX
History of connective tissue or musculoskeletal disorders
Biphosphonate therapy within the past 6 months
Acute renal failure
Serum creatinine equal to or higher than 4.5mg/dl
Positive serum pregnancy test in adolescent females

Study is for people with:

Chronic Lymphocytic Leukemia

Estimated Enrollment:

20

Study ID:

NCT00330538

Recruitment Status:

Completed

Sponsor:

Children's Mercy Hospital Kansas City

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There is 1 Location for this study

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Children's Mercy Hospital
Kansas City Missouri, 64108, United States

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Study is for people with:

Chronic Lymphocytic Leukemia

Estimated Enrollment:

20

Study ID:

NCT00330538

Recruitment Status:

Completed

Sponsor:


Children's Mercy Hospital Kansas City

How clear is this clinincal trial information?

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