Wednesday, November 19, 2025
5:00 PM – 6:00 PM UTC
12:00 PM – 1:00 PM EST
6:00 PM – 7:00 PM CET
Agenda:
- Introduction – Paolo Bossi, MD (Chair)
- The Experience of Nausea and Vomiting: How to Design a Clinical Predictor of a Treatment-Induced Adverse Effect – George Dranitsaris, PhD
Objectives:
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- Understand the steps in developing toxicity risk prediction tools in oncology, with a focus on nausea and vomiting
- Illustrate the clinical application of toxicity prediction tools in oncology
- Demonstrate how toxicity prediction tools can be used to improve the efficiency of clinical trials in oncology
- Predicting Oral and GI Toxicities in Supportive Oncology: Leveraging Clinical Data to Prevent Nutritional and Pain Consequences – Mellar Davis, MD
Objectives:
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- Drug-Related Genetic Risk Assessment: identify DPYD variants associated with 5-FU and capecitabine toxicity UGT1A1 conjugate associated with irinotecan mucositis and diarrhea
- Individual Genomic Risk Factors: name at least 3 of the 4 categories of individual genetic risks: drug transporters, genes involved in DNA repair, inflammatory signalling pathways, epithelial healing genes
- Clinical Application: correctly sequence opioid selection as: First line: Morphine (preferred over oxycodone). Second line: Buprenorphine and hydromorphone (preferred over methadone, all three preferred over fentanyl). Contraindicated: Codeine and tramadol (due to CYP2D6 dependence)
- Treatment Protocol: identify benzylamine as the preferred initial intervention before morphine (where available)
- Emerging Predictors of Oral and GI Toxicities: From Biological and Microbiome-based Models to AI Models – Akshat Singhal, PhD
Objectives:
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- Describe the significance of biologically-informed AI models in patient care, including treatment and toxicity prediction
- Examine a chemotherapy resistance model and discuss methods to extend such models for toxicity prediction
- Q&A
- Closing Remarks
Financial support provided by Nestlé Health Science.
For US only Dietitians and Registered Nurses:
One CPEU is awarded in accordance with the Commission on Dietetic Registration’s CPEU Prior Approval Program for US Registered Dietitians. Provider #NE008.
Funding from non-CPE revenue for CPE planning, development, review, and / or presentation has been provided by Nestlé Health Science.
One contact hour is available for US Registered Nurses. Nestlé Health Science is a Continuing Education Provider approved by the California Board of Registered Nursing, Provider #11366.
There is no charge for attending this program.
Speakers:

Paolo Bossi, MD (Chair)

George Dranitsaris, PhD

Mellar Davis, MD

Akshat Singhal, PhD