Mostafa Mohamed

Research Assistant Professor

University of Rochester Medical Center
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Mostafa Mohamed is a Research Assistant Professor at the University of Rochester Medical Center in the United States. His research focuses on the impact of systemic therapy on older adults with advanced cancer, emphasizing the associations between patient-reported toxicities, frailty, and physical well-being. Recent publications include studies on polypharmacy, cognitive function, and communication about aging-related concerns in oncological settings.

Articles (11)

Year:

2025

Year:

2024

Year:

2023

Background Polypharmacy is common in older adults who are starting cancer treatment and is associated with an increased risk of potentially inappropriate medications (PIMs) and potential drug‐drug interactions (PDIs). The authors evaluated the association of medication measures with adverse outcomes in older adults with advanced cancer who were receiving systemic therapy. Methods This secondary analysis from GAP 70+ Trial (ClinicalTrials.gov identifier NCT02054741; principal investigator, Supriya G. Mohile) enrolled patients aged 70 years and older with advanced cancer who planned to start a new treatment regimen ( n = 718). Polypharmacy was assessed before the initiation of treatment and was defined as the concurrent use of eight or more medications. PIMs were categorized using 2019 Beers Criteria and the Screening Tool of Older Persons' Prescriptions. PDIs were evaluated using Lexi‐Interact Online. Study outcomes were assessed within 3 months of treatment and included: (1) the number of grade ≥2 and ≥3 toxicities according to the National Cancer Institute Common Toxicity Criteria, (2) treatment‐related unplanned hospitalization, and (3) early treatment discontinuation. Multivariable regression models examined the association of medication measures with outcomes. Results The mean patient age was 77 years, and 57% had lung or gastrointestinal cancers. The median number of medications was five (range, 0–24 medications), 28% of patients received eight or more medications, 67% received one or more PIM, and 25% had one or more major PDI. The mean number of grade ≥2 toxicities in patients with polypharmacy was 9.8 versus 7.7 in those without polypharmacy (adjusted β = 1.87; standard error, 0.71; p <.01). The mean number of grade ≥3 toxicities in patients with polypharmacy was 2.9 versus 2.2 in patients without polypharmacy (adjusted β = 0.59; standard error, 0.29; p = .04). Patients with who had one or more major PDI had 59% higher odds of early treatment discontinuation (odds ratio, 1.59; 95% confidence interval, 1.03–2.46; p = .03). Conclusions In a cohort of older adults with advanced cancer, polypharmacy and PDIs were associated with an increased risk of adverse treatment outcomes. Providing meaningful screening and interventional tools to optimize medication use may improve treatment‐related outcomes in these patients.

Year:

2023

Year:

2022

Year:

2022

Year:

2022

Year:

2022

Year:

2020

Year:

2020

Year:

2020

Collaborators (7)

Kah Poh Loh

University of Rochester Medical Center

UNITED STATES
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Eva Culakova

Research Assistant Professor

University of Rochester

UNITED STATES
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Marie Flannery

Associate Professor

University of Rochester

UNITED STATES
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Nikesha Gilmore

Assistant Professor

University of Rochester Medical Center

UNITED STATES
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Amber Kleckner

University of Maryland

UNITED STATES
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Erika E. Ramsdale

-

UNITED STATES
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HUIWEN XU

Assistant Professor

University of Texas Medical Branch at Galveston

UNITED STATES
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