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Abstract Details

Examining Rates of Pseudoprogression in Older Patients with Glioblastoma
Neuro-oncology
P6 - Poster Session 6 (8:00 AM-9:00 AM)
5-013
Determine whether older patients with Glioblastoma (GBM) who receive a hypofractionated course of radiation therapy (HfRT= 40 cGy in 15 fractions) have higher rates of pseudoprogression (PsP) than those who receive the standard course (60 cGy in 30 fractions) of radiation therapy (RT).
Older adults (>/=65) with GBM often receive HfRT to reduce time toxicity. We hypothesized that higher RT doses per fraction may increase the likelihood of developing PsP. 

IRB-approved retrospective analysis of older adults with GBM diagnosed from 2019-2022. Records were reviewed to describe clinical variables, radiation course, development of PsP by RANO criteria, and interventions to manage symptomatic pseudoprogression. Pearson’s chi-squared test was used to determine an association between course of treatment, development of PsP, receipt of temozolomide (TMZ), and clinical interventions.

50 patients were identified (29 M), median age =74 (range 69-95), median KPS 80 (range 60-100), median overall survival (OS) was 12 months. 23 patients were MGMT methylated, 22 unmethylated, and 5 indeterminate. MGMT methylation status was not predictive of PsP. 28/50 had gross total resection. 32/50 received HfRT and 21 of these 32 also received TMZ, vs. 16/18 in the standard RT group. 56.25% of pts receiving HfRT developed pseudoprogression compared to 44.44% in the standard RT group (p=0.42). Among pts receiving HfRT, addition of TMZ was associated with PsP (p=0.10). Pts who developed PsP were more likely to require clinical interventions if they received HfRT compared to standard RT (p=0.11).

HfRT did not clearly increase risk of pseudoprogression, but our findings suggest that addition of TMZ may increase risk of pseudoprogression in older patients. Greater statistical power or a prospective cohort study would allow evaluation of whether certain chemoradiation regimens increase the likelihood of pseudoprogression development.

Authors/Disclosures
Derek L. Chien
PRESENTER
Mr. Chien has nothing to disclose.
Sara Hardy, MD (University of Washington) Dr. Hardy has received research support from the American Cancer Society.
Jennifer N. Serventi, PA (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.
Nimish A. Mohile, MD, FAAN The institution of Dr. Mohile has received research support from Novocure.
Lauryn Hemminger (Strong Memorial Hospital) Dr. Hemminger has received personal compensation in the range of $500-$4,999 for serving as a Consultant for Alexion.