Predictors of low and very low bone mineral density in long‐term childhood acute lymphoblastic leukemia survivors: Toward personalized risk prediction

Author:

Nadeau Geneviève123ORCID,Samoilenko Mariia1,Fiscaletti Melissa12,Veilleux Louis‐Nicolas4ORCID,Curnier Daniel125ORCID,Laverdière Caroline126,Sinnett Daniel12,Krajinovic Maja127,Lefebvre Geneviève8,Alos Nathalie123

Affiliation:

1. CHU Sainte‐Justine Research Centre University of Montreal Montreal Quebec Canada

2. Department of Pediatrics Faculty of Medicine University of Montreal Montreal Quebec Canada

3. Division of Endocrinology Sainte‐Justine University Hospital Centre Montreal Quebec Canada

4. Montreal Shriners Hospital for Children Montreal Quebec Canada

5. School of Kinesiology Faculty of Medicine University of Montreal Montreal Quebec Canada

6. Division of Hemato‐Oncology Sainte‐Justine University Hospital Centre Montreal Quebec Canada

7. Department of Pharmacology University of Montreal Montreal Quebec Canada

8. Department of Mathematics UQAM Montreal Quebec Canada

Abstract

AbstractBackgroundCohorts of childhood acute lymphoblastic leukemia (cALL) survivors reaching adulthood are increasing. Approximately 30% of survivors meet criteria for low bone mineral density (BMD) 10 years after diagnosis. We investigated risk factors for low BMD in long‐term cALL survivors.MethodsWe recruited 245 cALL survivors from the PETALE (Prévenir les effets tardifs des traitements de la leucémie aiguë lymphoblastique chez l'enfant) cohort, who were treated with the Dana Farber Cancer Institute protocols, did not experience disease relapse or hematopoietic stem cell transplants, and presented with more than 5 years of event‐free survival. Median time since diagnosis was 15.1 years.ResultsPrevalence of low DXA‐derived BMD (Z‐score ≤−1) ranged between 21.9% and 25.3%, depending on site (lumbar spine (LS‐BMD), femoral neck (FN‐BMD), and total body (TB‐BMD), and between 3.7% and 5.8% for very low BMD (Z‐score ≤−2). Males had a higher prevalence of low BMD than females for all three outcomes (26%–32% vs. 18%–21%), and male sex acted as a significant risk factor for low BMD in all models. Treatment‐related factors such as cumulative glucocorticoid (GC) doses and cranial radiation therapy (CRT) were associated with lower BMDs in the full cohort and in females at the FN‐BMD site.ConclusionLow and very low BMD is more prevalent in male cALL survivors. Male sex, high cumulative GC doses, CRT, risk group, and low body mass index (BMI) were identified as risk factors for low BMD. A longer follow‐up of BMD through time in these survivors is needed to establish if low BMD will translate into a higher risk for fragility fractures through adulthood.

Funder

Garron Family Cancer Centre

Cancer Research Society

Canadian Institutes of Health Research

CHU Sainte-Justine Foundation

C17 Children's Cancer and Blood Disorders

Canadian Cancer Society Research Institute

Pediatric Oncology Group of Ontario

Publisher

Wiley

Reference40 articles.

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2. Cancer facts and figures.American Cancer Society;2014. Accessed November 15 2022.http://www.cancer.gov/types/leukemia/hp/child‐all‐treatment‐pdq#cit/section_1.5

3. Clinical Ascertainment of Health Outcomes Among Adults Treated for Childhood Cancer

4. Topics in pediatric leukemia–acute lymphoblastic leukemia and late effects in long‐term survivors;Casillas J;MedGenMed,2005

5. Endocrine Late Effects in Childhood Cancer Survivors

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