Optimizing the G8 Screening Tool for Older Patients With Cancer: Diagnostic Performance and Validation of a Six-Item Version

Author:

Martinez-Tapia Claudia1,Canoui-Poitrine Florence12,Bastuji-Garin Sylvie123,Soubeyran Pierre45,Mathoulin-Pelissier Simone67,Tournigand Christophe89,Paillaud Elena110,Laurent Marie110,Audureau Etienne12,

Affiliation:

1. a EA 7376 CEpiA (Clinical Epidemiology and Ageing Unit), IMRB, A-TVB DHU

2. c Public Health Department, Assistance Publique Hôpitaux de Paris, Henri-Mondor Hospital, Créteil, France

3. d Clinical Research Unit (URC Mondor), Assistance Publique Hôpitaux de Paris, Henri-Mondor Hospital, Créteil, France

4. g Department of Medical Oncology, Institut Bergonié, Bordeaux, France

5. h Université de Bordeaux, Bordeaux, France

6. i INSERM U897, CIC-EC07, ISPED, Université de Bordeaux, France

7. j Clinical and Epidemiological Research Unit, Institut Bergonié, Bordeaux, France

8. b EC2M3 Unit, VIC DHU, Université Paris Est (UPE)

9. e Department of Medical Oncology Assistance Publique Hôpitaux de Paris, Henri-Mondor Hospital, Créteil, France

10. f Internal Medicine and Geriatric Department, Assistance Publique Hôpitaux de Paris, Henri-Mondor Hospital, Créteil, France

Abstract

Abstract Background. A multidimensional geriatric assessment (GA) is recommended in older cancer patients to inventory health problems and tailor treatment decisions accordingly but requires considerable time and human resources. The G8 is among the most sensitive screening tools for selecting patients warranting a full GA but has limited specificity. We sought to develop and validate an optimized version of the G8. Patients and Methods. We used a prospective cohort of cancer patients aged ≥70 years referred to geriatricians for GA (2007–2012: n = 729 [training set]; 2012–2014: n = 414 [validation set]). Abnormal GA was defined as at least one impaired domain across seven validated tests. Multiple correspondence analysis, multivariate logistic regression, and bootstrapped internal validation were performed sequentially. Results. The final model included six independent predictors for abnormal GA: weight loss, cognition/mood, performance status, self-rated health status, polypharmacy (≥6 medications per day), and history of heart failure/coronary heart disease. For the original G8, sensitivity was 87.2% (95% confidence interval, 84.3–89.7), specificity 57.7% (47.3–67.7), and area under the receiver-operating characteristic curve (AUROC) 86.5% (83.5–89.6). The modified G8 had corresponding values of 89.2% (86.5–91.5), 79.0% (69.4–86.6), and 91.6% (89.3; 93.9), with higher AUROC values for all tumor sites and stable properties on the validation set. Conclusion. A modified G8 screening tool exhibited better diagnostic performance with greater uniformity across cancer sites and required only six items. If these features are confirmed in other settings, the modified tool may facilitate selection for a full GA in older patients with cancer.

Funder

French National Cancer Institute

Geriatric Oncologic Unit

Publisher

Oxford University Press (OUP)

Subject

Cancer Research,Oncology

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