Fosamax for Childhood Cancer Survivors

Osteoporosis Clinical Trial

Official title:

Randomized Controlled Study on the Benefits and Safety of Bisphosphonate Treatment in Childhood Cancer Survivors

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT00391404
• Other study ID #: HK-CCFGrants2005.TFL
• Status: Recruiting
• Phase: Phase 3
• First received: October 23, 2006
• Last updated: May 22, 2008
• Start date: May 2006
• Est. completion date: October 2008

Study information

• Verified date: May 2008
• Source: Chinese University of Hong Kong
• Contact: Ting Fan Leung, MBChB, MD
• Phone: 852-2632 2981
• Email: tfleung[@]cuhk.edu.hk
• Is FDA regulated: No
• Health authority: Hong Kong: Joint CUHK-NTEC Clinical Research Ethics Committee
• Study type: Interventional

Clinical Trial Summary

Survivors of childhood cancers face a variety of long-term problems. The investigators' recent study found that osteoporosis and osteopenia were common among these patients. The factors leading to, as well as the best treatment option for, this morbidity are unclear. Bisphosphonates are currently the standard therapy for osteoporosis in the elderly. However, the efficacy and safety of bisphosphonates for treating osteoporosis in long-term cancer survivors have not been tested. The investigators hypothesize that alendronate, an orally active bisphosphonate, is efficacious and safe in the treatment of osteoporosis in these patients.

Description:

The modern treatment for childhood malignancy includes surgery and chemoradiotherapy either individually or in combination. Despite the great achievement in improving patient survival, these treatments also greatly enhance the adverse effects on the unfortunate children. Our research group has recently conducted a pioneer study on the bone mineralization and bone mineral density (BMD) study in longterm childhood cancer survivors in local patients who have completed anti-cancer treatment for at least five years. This landmark study showed that persistent treatment-related adverse effects on skeletal development are common (up to 50%) in local long-term survivors of childhood cancers. Thus, it is important during this critical period of rapid somatic growth in adolescents and young adults that these cancer survivors achieve their peak potential for bone mineralization and strengthening. In this proposed study, we investigate with a randomized and controlled study design on the efficacy of a second-generation oral bisphosphonate, alendronate, to improve BMD over a 36-week period in long-term survivors of childhood cancers in Hong Kong. In addition to alendronate, all subjects in the active and control groups will receive alfacalcidol (vitamin D) and calcium carbonate throughout the whole study period. The study results will help paediatric oncologists to decide on the optimal remedial treatments against osteoporosis in long-term cancer survivors.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 100
• Est. completion date: October 2008
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 15 Years and older

Eligibility

Inclusion Criteria:

• Chinese patients who completed treatments for childhood cancers for at least 5 years

• Currently followed up in the Department of Paediatrics of Prince of Wales Hospital

• Younger than 18 years old at the time of diagnosis of underlying cancers

• Evidence of osteoporosis (i.e. BMD T- or Z-score < -2.5 at lumbar spine)

• Older than 15 years of age at the time of recruitment

Exclusion Criteria:

• Current treatment (i.e. within 6 months) with maintenance systemic or high-dose inhaled corticosteroids

• Subjects who cannot cooperate for BMD measurements

• Pregnant female patients

• Subjects with prior history of allergy to alendronate or in whom alendronate treatment is contraindicated

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Osteoporosis

Intervention

Drug:
• Alendronate
Alendronate 70 mg weekly (oral)
• Placebo
Placebo

Locations

Country	Name	City	State
Hong Kong	Prince of Wales Hospital, Shatin, N.T.	Hong Kong

Sponsors (1)

Lead Sponsor	Collaborator
Chinese University of Hong Kong

Country where clinical trial is conducted

Hong Kong, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	The percent change in bone mineral density (BMD) at lumbar spine at 36-weeks in subjects who receive active and control treatments		36 weeks
Secondary	Changes in BMD at femoral neck		36 weeks
Secondary	Changes in biochemical markers of bone turnover		36 weeks
Secondary	Occurrence of clinical bone-related symptoms at 12-weeks and end of this study		36 weeks