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Abstract Details

Association of Frailty and Survival After Treatment in Older Patients with Glioblastoma
Neuro-oncology
S27 - Neuro-oncology (4:18 PM-4:30 PM)
005

Older adults are a heterogeneous population. Frailty, the accumulation of deficits that increase vulnerability to stressors, may underly some of this heterogeneity. However, there are scant data on frailty in patients with glioblastoma.

We aimed to characterize frailty in patients ≥65 years old with glioblastoma using a deficit accumulation frailty index (DAFI) score and examine the association of frailty and treatment with overall survival (OS).

We prospectively enrolled 30 patients with glioblastoma and calculated a DAFI score based on a 45-item scale. Using standard cutoffs, patients were categorized as non-frail, pre-frail, or frail. Patients were treated per multidisciplinary consensus and followed every 2 months. OS (months from diagnosis) was compared between groups using the log-rank test. Cox regressions assessed multiple predictors for survival. Model fit was described by AIC (smaller is better).

For all (median age 73.9, median follow up 11.1 months), median OS with conventional chemoradiation was 17.5 months, hypofractionated chemoradiation was 14.0 months, and radiation alone was 7.0 months (p=0.0002). Median OS was 17.5 months for non-frail patients (n=15), 11.2 months for pre-frail patients (n=11), and 7.9 months for frail patients (n=4, p=0.008). In non-frail patients, median OS for conventional chemoradiation was not reached, hypofractionated chemoradiation was 15.0 months, and radiation alone was 9.7 months (p=0.04). Non-frail patients (40% MGMT methylated) treated with chemotherapy (temozolomide) had a median OS of 25 vs 9.7 months without chemotherapy (p=0.02). Models using frailty alone predicted survival (AIC= 99) better than a combined model using KPS, MGMT methylation, and age (AIC= 112).

Non-frailty was associated with longer survival; in older patients receiving conventional chemoradiation, survival approached that of younger patients. Frailty also predicted survival better than a combined model using KPS, MGMT methylation, and age. Frailty may be a superior to age and KPS in guiding decisions regarding glioblastoma treatment.

Authors/Disclosures
Sara Hardy (University of Rochester)
PRESENTER
Dr. Hardy has received research support from the American Cancer Society.
No disclosure on file
Lauryn Hemminger (Strong Memorial Hospital) Dr. Hemminger has nothing to disclose.
No disclosure on file
Sarah Cawley Miss Cawley has nothing to disclose.
Jennifer Serventi (University Of Rochester Medical Center) Ms. Serventi has received personal compensation in the range of $10,000-$49,999 for serving on a Speakers Bureau for Novocure.
Jacqueline Behr (University of Rochester Medical Center) Mrs. Behr has nothing to disclose.
No disclosure on file
No disclosure on file
Nimish Mohile Dr. Mohile has nothing to disclose.