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Risk Evaluation and Mitigation Strategies (REMS) for oral oncolytics: Increased safety or barrier to access?
Vincent Harris1, Ming-Hei Tai2
1Department of Pharmacy, Atrium Health Levine Cancer Institute, Charlotte, NC, USA.
Abstract:
Many oral oncolytics inhibit rapidly dividing cells and are teratogenic. However, only a few agents are restricted under a Risk Evaluation and Mitigation Strategies (REMS) program due to embryo-fetal toxicity. The benefit of a REMS program for only select oral oncolytics is unclear.
Insights
Many oral cancer drugs harm developing fetuses and require special Risk Evaluation and Mitigation Strategies (REMS). It is unclear if restricting only some oral oncolytics under REMS benefits patients.
Area of Science:
- Oncology
- Pharmacology
- Teratology
Background:
- Oral oncolytics target rapidly dividing cells, leading to potential teratogenicity.
- Risk Evaluation and Mitigation Strategies (REMS) are implemented for select oral oncolytics with demonstrated embryo-fetal toxicity.
- The specific benefit of REMS for a limited subset of oral oncolytics remains uncertain.
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