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Abstract Details

Medical Comorbidities as Predictors of Survival in Glioblastoma
Neuro-oncology
P6 - Poster Session 6 (8:00 AM-9:00 AM)
5-014

To retrospectively assess medical comorbidities as determinants of survival in glioblastoma patients. 

Glioblastoma accounts for over half of primary malignant brain tumors in adults. Five-year survival is <10%. Age, neurologic performance, extent of resection, and certain molecular markers are known to influence patient survival. The impact of medical comorbidities requires further investigation. 

All patients with glioblastoma treated at Rhode Island Hospital between 2005 and 2021 were identified from the Lifespan Cancer Center database. Demographic information was extracted together with pathology and tumor-related molecular data. Comorbidities at diagnosis, including hypertension, hyperlipemia, and diabetes were tabulated. Additionally, clinical information on resolved or concurrent malignancies was documented. Comparisons between groups were conducted using Kaplan-Meier survival statistics and Kruskal-Wallis testing with correction for multiple comparisons. 

The analysis included 868 glioblastoma patients (56.5% male, 43.2% female). Comorbidity incidence rates were 57.5% for hypertension, 47.9% for hyperlipidemia, 15.8% for type 2 diabetes mellitus (T2DM), and 16.5% for other malignancies. Hypertensive patients had a lower median overall survival (mOS) compared to non-hypertensive patients, 9 (95% CI 8–11) vs. 14 (95% CI 12–16) months, respectively (p<0.001). Decreased mOS was noted in patients with hyperlipidemia compared to those without, 9 (95% CI 8–11) vs. 13 (95% CI 11–14) months, respectively (p<0.001). Patients with T2DM had a shortened mOS compared to non-diabetic patients, 7 (95% CI 6–10) vs. 12 (95% CI 11–13) months, respectively (p<0.001). Those with past or contemporaneous cancer history had a mOS of 9 (95% CI 7–11) months, compared to 12 (95% CI 11–13) months in those without (p=0.01).

Hypertension, hyperlipidemia, T2DM, and additional malignancies significantly correlate with decreased survival of glioblastoma patients. Therapeutic trials for these patients should account for the influence of medical comorbidities on treatment efficacy. 

Authors/Disclosures
Justin D. Bessette (The Warren Alpert Medical School of Brown University)
PRESENTER
Mr. Bessette has nothing to disclose.
Julia Noreck Julia Noreck has nothing to disclose.
Robert Edwards (Lifespan Cancer Institute) No disclosure on file
William Siwik No disclosure on file
Tara Szymanski (Rhode Island Hospital) No disclosure on file
Eric T. Wong, MD, FAAN (Rhode Island Hospital) Dr. Wong has received personal compensation in the range of $500-$4,999 for serving as a Consultant for Novocure. Dr. Wong has received personal compensation in the range of $500-$4,999 for serving as a Consultant for ZaiLab. Dr. Wong has received personal compensation in the range of $500-$4,999 for serving as a Consultant for Turning Point Therapeutics. Dr. Wong has received personal compensation in the range of $500-$4,999 for serving as a Consultant for Imvax. The institution of Dr. Wong has received personal compensation in the range of $5,000-$9,999 for serving on a Scientific Advisory or Data Safety Monitoring board for Novocure. The institution of Dr. Wong has received personal compensation in the range of $500-$4,999 for serving on a Scientific Advisory or Data Safety Monitoring board for Turning Point Therapeutics. The institution of Dr. Wong has received research support from Novocure. Dr. Wong has received intellectual property interests from a discovery or technology relating to health care. Dr. Wong has received publishing royalties from a publication relating to health care.