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Osteoporosis in Pediatric Cancer

Patients

Allana Boone

Definitions
Osteopenia:

BMD less than normal peak


BMD, but not enough to be classified as
Osteoporosis.

Osteopenia

places individuals at increased


risk of eventually developing osteoporosis

Definitions
Osteoporosis:

Greek; porous bones


ostoun = bone, poros = pore
Progressive bone disease that is
characterized by a decrease in bone
mass/density, deteriorated architecture and
altered mineral content, which can lead to
increased risk of fractures.

Childhood Cancer1,2
1

in 1,000 young adults is a Cancer survivor

Acute

lymphoblastic leukemia (ALL) is the


most commonly diagnosed cancer in children

Overall

long-term survival rate of ALL ~80%

Prevalence of Osteoporosis3
Osteoporosis:
In 1996, 28 million Americans affected by osteoporosis
Estimated 41 million affected in 2015 (NOF)
1.5 million fractures in 1996, costing $14 billion
Predicted 2.25 million fractures costing $60 billion (NOF)
Low BMD in Pediatric Population:
21 65% of survivors
The National Osteoporosis Foundation (NOF)

Why are Pediatric Cancer Patients


at Increased Risk?
Chemotherapy
Radiation

therapy
Corticosteroids
Nutrition status
Physical Inactivity esp. weight bearing
Limited sun exposure
Vitamin D Insufficiency/Deficiency (VDI/VDD)*

Research3

Objective3
Determine

the prevalence of VDI/VDD in


pediatric patients treated with corticosteroids
in comparison to healthy controls. Identify
associations between VDI/VDD with known
risk factors of vitamin D abnormalities, such
as age, race, season, and elevated BMI.

Participants3
Vanderbilt

Pediatric Endocrinology Clinic


171 cancer patients <23 yrs old at diagnosis

97

Treatment with corticosteroids >/=28 days


Feb 08 September 11

healthy controls 0-21 yrs old


June 10 Jan 13
Exclusion criteria noted on next slide

Exclusion Criteria: Healthy Controls3

Excluded patients with diagnosis/prior diagnosis of:

Osteopenia/Osteoporosis
Osteogenesis perfecta
Diagnosed VDI/VDD
>2 bone fractures x past 2 yrs
Chronic or current corticosteroid use
Thyrotoxicosis
Malabsorption disorders
DM
Hx of malignancy/current Dx of malignancy
Non-weight bearing status

Methods3
Medical

record review
Anthropometrics
Liquid chromatography/tandem mass
spectrometry
DXA scan
Statistical Analysis: univariate analysis,
multiple logistic regression models,

Results3

Results3

Results

Interventions
Adequate

dietary vitamin D OR
supplementation (D3)
Encouraging weight bearing exercises
Adequate Ca intake OR supplementation

Careful with supplements and renal patients

Endocrine

consult -- patients with reported


frequent fractures or diagnosis of
osteoporosis

AAP: Vitamin D Recommendation


In

2008, the American Academy of Pediatrics


increased its recommended daily intake of
vitamin D in infants, children, and
adolescents to 400 IU.

No

evidence suggests that this


recommendation is adequate or toxic

Childrens Oncology Group (COG)


Long-term Follow-Up Recommendation:
Begin screening all childhood cancer
survivors ~2 years after completion of
treatment (in remission)
DXA scan
CT scan
Subjective information

Conclusions

Increasing number of cases of pediatric patients with


BMD loss (osteopenia/osteoporosis)
Osteoporosis: global public health problem
Treatments associated with pediatric oncology can
increase risk of BMD loss
Vitamin D/Ca status may predict risk of BMD loss
Exercise and good nutrition are important players in
decreasing risk of BMD loss

Implications for Clinical Practice

Importance of timely interventions I.e. adequate


nutrition, increased exercise, supplementation,
Endocrine consults, DXA/CT scans

Need for more research

References

Simmons JH, Chow EJ, Koehler E, et al. Significant 25-hydroxyvitamin D deficiency in child and adolescent survivors of acute
lymphoblastic leukemia: treatment with chemotherapy compared with allogeneic stem cell transplant. Pediatric blood & cancer.
2011;56:1114-1119.
Mandel K, Atkinson S, Barr RD, Pencharz P. Skeletal Morbidity in Childhood Acute Lymphoblastic Leukemia. Journal of Clinical
Oncology. 2004;22:1215-1221.
Esbenshade AJ, Sopfe J, Zhao Z, et al. Screening for vitamin D insufficiency in pediatric cancer survivors. Pediatric Blood &
Cancer. 2014;61:723-728.
den Hoed MAH, Klap BC, te Winkel ML, et al. Bone mineral density after childhood cancer in 346 long-term adult survivors of
childhood cancer. Osteoporosis Int. 2015;26:521-529
Bianchi M. Glucorticoids and Bone: Some General Remarks and Some Special Observations in Pediatric Patients. Calcif Tissue
Int. 2002;70:384-390.
Modan-Moses D, Pinhas-Hamiel O, Munitz-Shenkar D, Temam V, Kanety H, Toren A. Vitamin D status in pediatric patients with a
history of malignancy. Pediatr Res. 2012;72:620.
Kulie T, Groff A, Redmer J, Hounshell J, Schrager S. Vitamin D: an evidence-based review. Journal of the American Board of
Family Medicine : JABFM. 2009;22:698-706.
El-Hajj Fuleihan G, Muwakkit S, Arabi A, et al. Predictors of bone loss in childhood hematologic malignancies: a prospective study.
Osteoporosis Int. 2012;23:665-674.
Arikoski P, Krger H, Riikonen P, Parviainen M, Voutilainen R, Komulainen J. Disturbance in bone turnover in children with a
malignancy at completion of chemotherapy. Med Pediatr Oncol. 1999;33:455-461.
Ward LM. Osteoporosis due to Glucocorticoid Use in Children with Chronic Illness. Horm Res. 2005;64:209-221.
Malaguti-Boyle M. How does vitamin D improve the management of cancer?: A literature review. Journal of the Australian
Traditional-Medicine Society. 2014;20:182-187.

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