Fracture Risk Prediction Using the Fracture Risk Assessment Tool in Individuals With Cancer.


Journal

JAMA oncology
ISSN: 2374-2445
Titre abrégé: JAMA Oncol
Pays: United States
ID NLM: 101652861

Informations de publication

Date de publication:
03 Oct 2024
Historique:
medline: 3 10 2024
pubmed: 3 10 2024
entrez: 3 10 2024
Statut: aheadofprint

Résumé

The Fracture Risk Assessment Tool (FRAX) is a fracture risk prediction tool for 10-year probability of major osteoporotic fracture (MOF) and hip fracture in the general population. Whether FRAX is useful in individuals with cancer is uncertain. To determine the performance of FRAX for predicting incident fractures in individuals with cancer. This retrospective population-based cohort study included residents of Manitoba, Canada, with and without cancer diagnoses from 1987 to 2014. Diagnoses were identified through the Manitoba Cancer Registry. Incident fractures to March 31, 2021, were identified in population-based health care data. Data analysis occurred between January and March 2023. FRAX scores were computed for those with bone mineral density (BMD) results that were recorded in the Manitoba BMD Registry. This study included 9877 individuals with cancer (mean [SD] age, 67.1 [11.2] years; 8693 [88.0%] female) and 45 877 individuals in the noncancer cohort (mean [SD] age, 66.2 [10.2] years; 41 656 [90.8%] female). Compared to individuals without cancer, those with cancer had higher rates of incident MOF (14.5 vs 12.9 per 1000 person-years; P < .001) and hip fracture (4.2 vs 3.5 per 1000 person-years; P = .002). In the cancer cohort, FRAX with BMD results were associated with incident MOF (HR per SD increase, 1.84 [95% CI, 1.74-1.95]) and hip fracture (HR per SD increase, 3.61 [95% CI, 3.13-4.15]). In the cancer cohort, calibration slopes for FRAX with BMD were 1.03 for MOFs and 0.97 for hip fractures. In this retrospective cohort study, FRAX with BMD showed good stratification and calibration for predicting incident fractures in patients with cancer. These results suggest that FRAX with BMD can be a reliable tool for predicting incident fractures in individuals with cancer.

Identifiants

pubmed: 39361310
pii: 2824314
doi: 10.1001/jamaoncol.2024.4318
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Auteurs

Carrie Ye (C)

Department of Medicine, University of Alberta, Edmonton, Alberta, Canada.

William D Leslie (WD)

Department of Medicine, University of Manitoba, Winnipeg, Manitoba, Canada.

Saeed Al-Azazi (S)

Department of Medicine, University of Manitoba, Winnipeg, Manitoba, Canada.

Lin Yan (L)

Department of Medicine, University of Manitoba, Winnipeg, Manitoba, Canada.

Lisa M Lix (LM)

Department of Medicine, University of Manitoba, Winnipeg, Manitoba, Canada.

Piotr Czaykowski (P)

Department of Medicine, University of Manitoba, Winnipeg, Manitoba, Canada.
CancerCare Manitoba, Winnipeg, Manitoba, Canada.

Eugene V McCloskey (EV)

Centre for Metabolic Bone Diseases, University of Sheffield Medical School, Sheffield, United Kingdom.

Helena Johansson (H)

Centre for Metabolic Bone Diseases, University of Sheffield Medical School, Sheffield, United Kingdom.
Mary McKillop Institute for Health Research, Australian Catholic University, Melbourne, Australia.

Nicholas C Harvey (NC)

MRC Lifecourse Epidemiology Unit, University of Southampton, Southampton, United Kingdom.
NIHR Southampton Biomedical Research Centre, University of Southampton and University Hospital Southampton NHS Foundation Trust, Southampton, United Kingdom.

John A Kanis (JA)

Centre for Metabolic Bone Diseases, University of Sheffield Medical School, Sheffield, United Kingdom.

Harminder Singh (H)

Department of Medicine, University of Manitoba, Winnipeg, Manitoba, Canada.
CancerCare Manitoba, Winnipeg, Manitoba, Canada.

Classifications MeSH