Prevention of Bone Loss After Pediatric Hematopoietic Cell Transplantation

Osteoporosis Clinical Trial

Official title:

Prevention of Bone Loss After Pediatric Hematopoietic Cell Transplantation

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02074631
• Other study ID #: 2013LS023
• Status: Completed
• Phase: Phase 2
• Start date: February 2015
• Est. completion date: October 6, 2022

Study information

• Verified date: January 2024
• Source: Masonic Cancer Center, University of Minnesota
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This is a Phase 2, open-label, randomized, controlled clinical study of pediatric subjects treated with pamidronate with calcium and vitamin D versus calcium and vitamin D alone following hematopoietic cell transplantation (HCT). The purpose of this study is to test the hypothesis that subjects receiving pamidronate with calcium and vitamin D will have higher lumbar spine bone mineral content (LBMC) measured by dual-energy X-ray tomography (DXA) at 1 year post-HCT than subjects receiving calcium and vitamin D alone (Control Group).

Recruitment information / eligibility

• Status: Completed
• Enrollment: 63
• Est. completion date: October 6, 2022
• Est. primary completion date: October 6, 2022
• Accepts healthy volunteers: No
• Gender: All
• Age group: 1 Year to 20 Years

Eligibility

Inclusion Criteria:

• Allogeneic hematopoietic cell transplant for hematologic malignancy (i.e. leukemia, lymphoma including ALL, AML, CML, NHL, HL) in complete remission; myelodysplastic syndrome (active dysplasia and/or blasts are permitted, but must not have active leukemia) or idiopathic severe aplastic anemia (SAA)
• Non-malignant diseases including idiopathic severe aplastic anemia (SAA) and other bone marrow failure disorders, hemoglobinopathies, adrenoleukodystrophy, immune deficiencies/dysregulation disorders who will be receiving myeloablative or reduced

toxicity preparative regimens that meet the following criteria:

• Regimens include those that are TBI based if the TBI dose is > 500cGy single dose or > 800cGy fractionated, or doses <500 cGy if combined with busulfan or treosulfan. These also include chemotherapy only based regimens that contain myeloablative doses of busulfan (>8mg/kg) or treosulfan without TBI.
• Patients with severe aplastic anemia are eligible regardless of conditioning regimen
• Myeloablative preparative regimen (for SAA any conditioning therapy allowed)
• Male or female =1 but = 20 years of age at time of study enrollment
• Patient or parent(s)/legal guardian(s) is able and willing to provide informed consent. Assent will be obtained per local institutional policy. Subjects who turn 18 during the course of the study will be consented at that time of their next visit by a member of the research staff.

Exclusion Criteria:

• History of a primary bone malignancy involving the lumbar spine
• Prior and/or planned concomitant medical therapy during the study period (through Day 360 post-HCT) with other bisphosphonates, Denosumab, or Teriparatide
• Pregnancy or breastfeeding - menstruating females must have a negative pregnancy test prior to study enrollment and agree to repeat pregnancy testing and contraception use per protocol as pamidronate is Pregnancy Category D - positive evidence of human fetal risk based on adverse reaction data
• Renal insufficiency, defined as creatinine level greater than the upper limit of normal for age
• Hereditary metabolic bone disease or skeletal dysplasia (e.g., osteopetrosis or OI) or primary hyperparathyroidism
• Other indications for HCT, including Fanconi anemia, other form of inherited bone marrow failure diseases, metabolic disorder, hemoglobinopathy, or immune deficiency
• Clinically significant fractures as defined by ISCD (a long bone fracture of the lower extremities, vertebral compression fracture, or two or more long bone fractures of the upper extremities) (88,89) indicated by a cast or a spine x-ray within the last 2 weeks
• Known or suspected allergy to pamidronate or related products
• Planned administration of an investigational study drug or agent that either can interact with pamidronate or have an independent effect on bone mineral density within the 4 weeks prior to randomization (Day 90) or planned use during study participation (Day 90 through Day 360)
• Impending invasive dental procedure that would be expected to occur during study participation (through Day 360)

Related Conditions & MeSH terms

• Bone Diseases, Metabolic
• Osteopenia
• Osteoporosis

Intervention

Drug:
• Pamidronate
Subjects randomized to pamidronate treatment will receive infusions, 1 mg/kg (to a max dose of 60mg) over 4 hours, every 3 months at approximately 100 days, 180 days, and 270 days after HCT.
• Calcium and vitamin D
All subjects will receive a standard recommended dose of 600 IU/day of vitamin D. Subjects who do not meet the RDA will receive additional calcium supplementation.

Locations

Country	Name	City	State
United States	University of Minnesota Amplatz Children's Hospital	Minneapolis	Minnesota
United States	Seattle Children's Hospital	Seattle	Washington

Sponsors (1)

Lead Sponsor	Collaborator
Masonic Cancer Center, University of Minnesota

Country where clinical trial is conducted

United States, 

References & Publications (55)

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* Note: There are 55 references in all — Click here to view all references

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Lumbar Spine Bone Mineral Content		1 year after HCT
Secondary	Total Body Bone Mineral Content (TBMC; Excluding Head; Adjusted for Height, Age, Sex, Tanner Stage, and Race)		1 year after HCT
Secondary	Total Bone Mineral Density (BMD), Cortical BMD, Trabecular BMD, and Estimated Bone Strength Measured by pQCT	Measured in g/cm2.	1 year after HCT
Secondary	Cytokine Levels (Interleukin IL-6, IL-7, and TNF-a)	Measured in pg/ml.	7 days, 14 days, 21 days, 90 days after HCT
Secondary	Receptor Activator of the Nuclear Factor-?B Ligand [RANKL], Osteoprotegerin [OPG]	Measured in pg/ml.	7 days, 14 days, 21 days, and 90 days after HCT
Secondary	Marker of Bone Resorption (Carboxy-terminal Collagen Crosslinks [CTX]	CTX measured in ng/ml.	7, 14, 21, 90, 180, 360 days after HCT
Secondary	Markers of Bone Formation (Procollagen Type 1 N-terminal Propeptide [P1NP])	P1NP measured in ng/ml.	7, 14, 21, 90, 180, 360 days after HCT
Secondary	Ratio of Receptor Activator of the Nuclear Factor-?B Ligand [RANKL] and Osteoprotegerin [OPG]		7 days, 14 days, 21 days, and 90 days after HCT
Secondary	Marker of Bone Resorption Deoxypyridinoline [DPD])	DPD measured in mmol/L.	7, 14, 21, 90, 180, 360 days after HCT
Secondary	Marker of Bone Formation Osteocalcin [OCN])	OCN measured in pg/ml.	7, 14, 21, 90, 180, 360 days after HCT