University of Michigan College of Pharmacy
The objective of the Hertz lab is to develop personalized cancer treatment approaches and translate them into clinical practice to optimize therapeutic outcomes in patients with cancer. Our research spans the translational spectrum from discovery through implementation. We identify clinical, kinetic, genetic, and physiologic predictors of cancer treatment efficacy and/or toxicity in retrospective analyses. These discoveries are integrated into novel tools that can be tested in prospective clinical trials to demonstrate that personalized cancer treatment enhances efficacy and/or prevents unnecessary toxicity.
My lab is accepting PhD students.
We investigate genetic variations in the DPYD gene that encodes the dihydropyrimidine dehydrogenase (DPD) enzyme to predict and prevent severe fluoropyrimidine toxicity in cancer patients, enabling safer and more personalized chemotherapy dosing strategies.
Real-world analysis of clinical outcomes from DPYD-guided dosing (OPREC)
Advocacy to increase clinical adoption of DPYD testing
Our laboratory identifies predictive biomarkers for chemotherapy-induced peripheral neuropathy (CIPN) to help oncologists personalize treatment and minimize this debilitating toxicity that affects quality of life in cancer survivors.
NCI R37 Grant: Discovery and validation of predictive biomarkers of CIPN using the SWOG S1714 cohort.
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For a complete list of publications, visit PubMed.
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We welcome inquiries from motivated students interested in clinical-translational cancer research. Please review the UM CPTS PhD Program or contact Dr. Hertz directly for other opportunities in our laboratory.