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

被引:2
作者
Ye, Carrie [1 ]
Leslie, William D. [2 ]
Al-Azazi, Saeed [2 ]
Yan, Lin [2 ]
Lix, Lisa M. [2 ]
Czaykowski, Piotr [2 ,3 ]
McCloskey, Eugene V. [4 ]
Johansson, Helena [4 ,5 ]
Harvey, Nicholas C. [6 ,7 ,8 ]
Kanis, John A. [4 ]
Singh, Harminder [2 ,3 ]
机构
[1] Univ Alberta, Dept Med, Edmonton, AB, Canada
[2] Univ Manitoba, Dept Med, Winnipeg, MB, Canada
[3] Canc Care Manitoba, Winnipeg, MB, Canada
[4] Univ Sheffield, Sch Med, Ctr Metabol Bone Dis, Sheffield, S Yorkshire, England
[5] Australian Catholic Univ, Mary McKillop Inst Hlth Res, Melbourne, Vic, Australia
[6] Univ Southampton, MRC Lifecourse Epidemiol Unit, Southampton, Hants, England
[7] Univ Southampton, NIHR Southampton Biomed Res Ctr, Southampton, Hants, England
[8] Univ Hosp Southampton NHS Fdn Trust, Southampton, Hants, England
基金
英国医学研究理事会;
关键词
ADMINISTRATIVE DATA; BONE HEALTH; VALIDATION; OSTEOPOROSIS;
D O I
10.1001/jamaoncol.2024.4318
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Importance 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. Objective To determine the performance of FRAX for predicting incident fractures in individuals with cancer. Design, Setting, and Participants 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. Main Outcomes and Measures FRAX scores were computed for those with bone mineral density (BMD) results that were recorded in the Manitoba BMD Registry. Results This study included 9877 individuals with cancer (mean [SD] age, 67.1 [11.2] years; 8693 [88.0%] female) and 45877 individuals in the noncancer cohort (mean [SD] age, 66.2 [10.2] years; 41656 [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. Conclusions and Relevance 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.
引用
收藏
页码:1554 / 1560
页数:7
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