Oncology Drug Reference Sheet: Eflornithine
Eflornithine (Iwilfin™) is the first U.S. Food and Drug Administration–approved oral maintenance therapy for high-risk neuroblastoma. Approved in December 2023, eflornithine has an orphan drug designation (https://voice.ons.org/news-and-views/fda-approves-eflornithine-for-adult-and-pediatric-patients-with-high-risk).
This ONS resource was produced for educational purposes only. Refer to the eflornithine prescribing information (https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=6716d8cc-66e6-4cee-935c-ccb85ed984f5) for full details.
DRUG INFORMATION | ||||
Classification | Targeted therapy (https://www.ons.org/huddle-cards/targeted-therapy-huddle-card)/enzyme inhibitor | |||
Mechanism of Action | Irreversible inhibition of the ornithine decarboxylase enzyme | |||
Indication | Reduces the risk of relapse in adult and pediatric patients with high-risk neuroblastoma who have demonstrated partial response to prior multiagent, multimodality therapy, including anti-GD2 immunotherapy | |||
ADMINISTRATION | ||||
Dosing, Frequency, and Duration | Dosing is based on body surface area (see prescribing information (https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=6716d8cc-66e6-4cee-935c-ccb85ed984f5) for full dosing instructions) and administered twice daily for up to two years or until patients experience disease progression or unacceptable toxicity. | |||
Route | Oral | |||
Safe Handling | Eflornithine is a potentially hazardous drug per the National Institute for Occupational Safety and Health definition (https://www.usp.org/compounding/general-chapter-hazardous-drugs-handling-healthcare#:~:text=The%20National%20Institute%20for%20Occupational,low%20doses%2C%20genotoxicity%2C%20or%20structure). Follow safe-handling precautions (https://www.ons.org/books/chemotherapy-and-immunotherapy-guidelines-and-recommendations-practice-second-edition). | |||
ADVERSE REACTIONS | ||||
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WARNINGS | ||||
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NURSING CONSIDERATIONS | ||||
Pretreatment | Obtain complete blood counts, liver function tests, pregnancy tests (as appropriate), and baseline audiograms. | |||
Administration | Instruct patients that they can take the medication with or without food and that the tablets may be swallowed whole, chewed, or crushed and mixed with two tablespoons of soft food or liquid. If they mix the medication in food, it must be consumed within an hour of mixing. | |||
During Treatment | Monitor complete blood counts, liver function tests, and hearing. | |||
PATIENT EDUCATION | ||||
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RESOURCES | ||||
Patient Resources | Patient-facing drug label (https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=6716d8cc-66e6-4cee-935c-ccb85ed984f5&audience=consumer) | |||
Healthcare Professional Resources | Clinical trial report (https://pubmed.ncbi.nlm.nih.gov/37883734/) Prescribing information (https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=6716d8cc-66e6-4cee-935c-ccb85ed984f5&audience=professional) |
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Other Resources | National Cancer Institute A to Z List of Cancer Drugs page (https://www.cancer.gov/about-cancer/treatment/drugs/eflornithine-hydrochloride) |