Validation of a frailty index in older cancer patients with solid tumours

被引:28
|
作者
McCarthy, A. L. [1 ,3 ]
Peel, N. M. [4 ]
Gillespie, K. M. [2 ]
Berry, R. [3 ]
Walpole, E. [3 ]
Yates, P. [2 ]
Hubbard, R. E. [4 ]
机构
[1] Univ Auckland, Sch Nursing, Auckland Mail Ctr, Private Bag 92019, Auckland 1142, New Zealand
[2] Queensland Univ Technol, Sch Nursing, Victoria Pk Rd, Kelvin Grove, Qld 4059, Australia
[3] Princess Alexandra Hosp, Canc Serv, 199 Ipswich Rd, Woolloongabba, Qld 4102, Australia
[4] Univ Queensland, Princess Alexandra Hosp, Ctr Res Geriatr Med, Level 2,Bldg 33,199 Ipswich Rd, Woolloongabba, Qld 4102, Australia
关键词
Geriatric oncology; Frailty; Comprehensive geriatric assessment; Chemotherapy; COMPREHENSIVE GERIATRIC ASSESSMENT; CHEMOTHERAPY TOXICITY; GUIDELINES; VALIDITY; ADULTS; SCALE; RISK; TOOL;
D O I
10.1186/s12885-018-4807-6
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Frailty is an indicator of physiological reserve in older people. In non-cancer settings, frailty indices are reliable predictors of adverse health outcomes. The aims of this study were to 1) derive and validate a frailty index (FI) from comprehensive geriatric assessment (CGA) data obtained in the solid tumour chemotherapy setting, and 2) to explore whether the FI-CGA could predict chemotherapy decisions and survival in older cancer patients with solid tumours. Methods: Prospective cohort study of a consecutive series sample of 175 cancer patients aged 65 and older with solid tumours. A frailty index was calculated using an accumulated deficits model, coding items from the comprehensive geriatric assessment tool administered prior to chemotherapy decision-making. The domains of physical and cognitive functioning, nutrition, mood, basic and instrumental activities of daily living, and comorbidities were incorporated as deficits into the model. Results: The FI-CGA had a right-skewed distribution, with median (interquartile range) of 0.27 (021-039). The 99% limit to deficit accumulation was below the theoretical maximum of 1.0, at 0.75. The FI-CGA was significantly related (p < 0.001) to vulnerability as assessed by the Vulnerable Elders Survey-13 and to medical oncologists' assessments of fitness or vulnerability to treatment Baseline frailty as determined by the FI-CGA was also associated with treatment decisions (Treatment Terminated, Treatment Completed, No Planned Treatment) (p < 0.001), with the No Planned Treatment group significantly frailer than the other two groups. Conclusion: The FI-CGA is a potentially useful adjunct to cancer clinical decision-making that could predict chemotherapy outcomes in older patients with solid tumours.
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页数:8
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