Affiliation:
1. Princess Máxima Center for Pediatric Oncology Utrecht The Netherlands
2. Department of Pediatric Physiotherapy Erasmus Medical Center‐Sophia Children's Hospital Rotterdam The Netherlands
3. Mathematical Institute Leiden University Leiden The Netherlands
4. Department of Biomedical Data Science, Section Medical Statistics Leiden University Medical Center Leiden The Netherlands
5. Department of Pediatrics, Division Pediatric Endocrinology, Obesity Center CGG Erasmus Medical Center‐Sophia Children's Hospital Rotterdam The Netherlands
6. Division of Child Health Wilhelmina Children's Hospital Utrecht The Netherlands
Abstract
AbstractBackgroundDexamethasone is important in the treatment for pediatric acute lymphoblastic leukemia (ALL) but induces muscle atrophy with negative consequences for muscle mass, muscle strength, and functional abilities. The aim of this study was to establish the effect of a dexamethasone course on sarcopenia and physical frailty in children with ALL, and to explore prognostic factors.MethodsPatients with ALL aged 3–18 years were included during maintenance therapy. Patients had a sarcopenia/frailty assessment on the first day of (T1) and on the day after (T2) a 5‐day dexamethasone course. Sarcopenia was defined as low muscle strength in combination with low muscle mass. Prefrailty and frailty were defined as having two or ≥three of the following components, respectively: low muscle mass, low muscle strength, fatigue, slow walking speed, and low physical activity. Chi‐squared and paired t‐tests were used to assess differences between T1 and T2. Logistic regression models were estimated to explore patient‐ and therapy‐related prognostic factors for frailty on T2.ResultsWe included 105 patients, 61% were boys. Median age was 5.3 years (range: 3–18.8). At T1, sarcopenia, prefrailty, and frailty were observed in respectively 2.8%, 23.5%, and 4.2% of patients. At T2, the amount of patients with frailty had increased to 17.7% (p = 0.002), whereas the number of patients with sarcopenia and prefrailty remained similar. Higher ASMM (odds ratio [OR]: 0.49, 95% CI: 0.28–0.83), stronger handgrip strength (OR: 0.41, 95% CI: 0.22–0.77) and more physical activity minutes per day (OR: 0.98, 95% CI: 0.96–0.99) decreased the risk of frailty at T2. Slower walking performance (OR: 2, 95% CI: 1.2–3.39) increased the risk. Fatigue levels at T1 were not associated with frailty at T2.ConclusionPhysical frailty increased strikingly after a 5‐days dexamethasone course in children with ALL. Children with poor physical state at start of the dexamethasone course were more likely to be frail after the course.
Funder
Stichting Kinderen Kankervrij
Subject
Cancer Research,Radiology, Nuclear Medicine and imaging,Oncology
Cited by
3 articles.
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