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RESEARCH PAPER ANALYSIS

Defining Cachexia in Children With Cancer in the United States: Developing a Framework to Inform Clinical and Research Practice.

Using SEER and Optum electronic health record data from 2017–2021, the study applied five candidate anthropometric or diagnostic-code criteria to 26,855 children with cancer and found that estimated cachexia prevalence and incidence varied substantially by definition, age, and cancer type.

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PMID42591002
JournalJournal of human nutrition and dietetics : the official journal of the British Dietetic Association
Publication Date2026-08-01
Ingested2026-08-17 12:23 AM
EXECUTIVE SUMMARY

What the AI sees

Using SEER and Optum electronic health record data from 2017–2021, the study applied five candidate anthropometric or diagnostic-code criteria to 26,855 children with cancer and found that estimated cachexia prevalence and incidence varied substantially by definition, age, and cancer type.

WHY IT MATTERS

Research significance

The study provides observational evidence for a framework to identify potential pediatric cancer cachexia; it is reasonable but unproven to infer that validated consensus criteria could enable earlier nutritional or supportive-care intervention and improve research stratification, as no treatment effect or clinical outcome benefit was tested.

ABSTRACT

Source abstract

BACKGROUND: Cancer cachexia describes the muscle and weight loss, anorexia, and physical impairment common in certain adult cancers. No formal criteria exist to define paediatric cancer cachexia, making its clinical recognition and impact largely unknown. Using established undernutrition guidelines, criteria were developed to identify potential cachexia in children with cancer based on standardised anthropometric measures or diagnostic codes. METHODS: The Surveillance, Epidemiology, and End Results and Optum Electronic Health Records databases were used to estimate prevalence and incidence rates of cancer and cancer cachexia between 2017 and 2021 in patients aged < 20 and < 18 years, respectively. In the absence of a consensus definition for paediatric cachexia, four sets of candidate criteria were developed based on body weight for length/height or body mass index z-scores, or reduced gain or loss of body weight, corresponding to mild or severe undernutrition. A fifth criterion required a potentially cachexia-related ICD-10-CM diagnosis code. RESULTS: This study included 26,855 paediatric patients (aged < 18 years) with cancer; ~90% were aged ≥ 2 years. Epidemiologic estimates for cancer cachexia prevalence and incidence rate varied considerably by age, cancer type and cachexia definition. Estimates were low for most categories, especially in the youngest age groups; however, cachexia was difficult to assess in patients aged < 2 years due to small patient numbers. CONCLUSIONS: We describe one of the first attempts to develop potential paediatric cachexia criteria. These criteria and resulting data provide a framework to inform further research into generating consensus guidelines for the identification of childhood cancer cachexia.

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European journal of pediatrics 65.14 28 Spinal ependymoma: a comprehensive review of molecular classification, management guidelines, and clinical outcomes with a focus on the pediatric population (Part III of ependymomas across compartments). Journal of neuro-oncology 70.9 29 Pediatric and Adult Sinonasal Phosphaturic Mesenchymal Tumors: CDKN2A Copy Number Alterations and Their Association with Recurrence. Head and neck pathology 57.5 30 Systematic review of the impact of germline mutations from unrelated bone marrow donors on post-allogeneic transplantation. Expert review of molecular diagnostics 64.09 31 Efficacy and safety of MEK inhibitors for NF1-associated symptomatic, inoperable plexiform neurofibromas: A systematic review and meta-analysis. PloS one 80.82 32 Eosinophilic angiocentric fibrosis in paediatric IgG4-related disease. BMJ case reports 55.2
PATIENT-FRIENDLY SUMMARY

Defining Cachexia in Children With Cancer in the United States: Developing a Framework to Inform Clinical and Research Practice.

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