Association Between Chronologic Age and Geriatric Assessment–Identified Impairments: Findings From the CARE Registry

Author:

Giri Smith123,Al-Obaidi Mustafa1,Weaver Alice3,Kenzik Kelly M.123,McDonald Andrew12,Clark Deanna1,Young-Smith Crystal3,Paluri Ravi23,Nandagopal Lakshmin23,Gbolahan Olumide23,Pergolotti Mackenzi45,Bhatia Smita12,Williams Grant R.123

Affiliation:

1. 1Institute for Cancer Outcomes and Survivorship,

2. 2O’Neal Comprehensive Cancer Center, and

3. 3Division of Hematology and Oncology, Department of Medicine, University of Alabama at Birmingham, Birmingham, Alabama;

4. 4Revital Cancer Rehabilitation, Select Medical, Mechanicsburg, Pennsylvania; and

5. 5Department of Occupational Therapy, Colorado State University, Fort Collins, Colorado.

Abstract

Background: The NCCN Guidelines for Older Adult Oncology recommend that, when possible, older adults with cancer undergo a geriatric assessment (GA) to provide a comprehensive health appraisal to guide interventions and appropriate treatment selection. However, the association of age with GA-identified impairments (GA impairments) remains understudied and the appropriate age cutoff for using the GA remains unknown. Patients and Methods: We designed a cross-sectional study using the Cancer and Aging Resilience Evaluation (CARE) registry of older adults with cancer. We included adults aged ≥60 years diagnosed with gastrointestinal malignancy who underwent a patient-reported GA prior to their initial consultation at the gastrointestinal oncology clinic. We noted the presence of GA impairments and frailty using Rockwood’s deficit accumulation approach. We studied the relation between chronologic age and GA impairments/frailty using Spearman rank correlation and chi-square tests of trend. Results: We identified 455 eligible older adults aged ≥60 years with gastrointestinal malignancies; the median age was 68 years (range, 64–74 years) and colorectal (33%) and pancreatic (24%) cancers were the most common cancer type. The correlation between chronologic age and number of geriatric impairments was weak and did not reach statistical significance (Spearman ρ, 0.07; P=.16). Furthermore, the prevalence of domain-specific impairments or frailty was comparable across the 3 age groups (60–64 years, 65–74 years, ≥75 years) with the exception of comorbidity burden. Notably, 61% of patients aged 60 to 64 years had ≥2 GA impairments and 35% had evidence of frailty, which was comparable to patients aged 65 to 74 years (66% and 36%, respectively) and ≥75 years (70% and 40%, respectively). Conclusions: Using chronologic age alone to identify which patients may benefit from GA is problematic. Future studies should identify screening tools that may identify patients at high risk of frailty and GA impairments.

Publisher

Harborside Press, LLC

Subject

Oncology

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