Amifostine serves two primary purposes in cancer treatment. Firstly, it is utilized to alleviate the distressing side effects of chemotherapy, particularly nausea and vomiting. Administered prior to chemotherapy sessions, it acts as a shield for healthy cells, diminishing the likelihood and severity of these gastrointestinal symptoms.

Secondly, amifostine is employed to counteract the adverse effects of radiation therapy on the salivary glands, specifically in patients undergoing treatment for head and neck cancers. 

By safeguarding these glands, it helps mitigate the uncomfortable condition of dry mouth, known as xerostomia, enhancing patient comfort and quality of life during radiotherapy.

Amifostine is a prodrug that is rapidly converted into its active form, a free thiol metabolite, in normal tissues. This metabolite acts as a scavenger of free radicals generated by chemotherapy or radiation therapy, protecting normal cells from damage while leaving cancer cells vulnerable to treatment.

Common side effects:

• Nausea and Vomiting: Amifostine may cause mild to moderate nausea and vomiting, especially during or shortly after administration. These symptoms usually subside on their own but can be managed with antiemetic medications if necessary.
• Hypotension: A drop in blood pressure (hypotension) is a common side effect of amifostine administration. Patients may experience dizziness, lightheadedness, or fainting due to decreased blood flow to the brain. Monitoring blood pressure before, during, and after treatment can help manage this side effect.
• Flushing: Some individuals may experience flushing or redness of the skin, particularly in the face and neck, as a result of amifostine infusion. This reaction is usually transient and resolves once the infusion is completed.

Serious side effects:

• Allergic Reactions: In rare cases, patients may experience allergic reactions to amifostine, characterized by symptoms such as rash, itching, swelling of the face or throat, difficulty breathing, or severe dizziness.
• Electrolyte Imbalances: Amifostine can cause electrolyte imbalances, including hypocalcemia (low calcium levels), hypomagnesemia (low magnesium levels), and hypokalemia (low potassium levels). These imbalances can lead to symptoms such as muscle cramps, weakness, irregular heartbeat, or seizures. Regular monitoring of electrolyte levels and appropriate supplementation may be necessary during treatment.

Patients should be educated about these potential side effects and instructed to report any unusual symptoms to their healthcare provider promptly. Close monitoring and supportive care can help manage side effects and ensure the safe and effective use of amifostine in cancer treatment.

Before initiating treatment with amifostine, healthcare providers should consider several precautions to ensure patient safety. Firstly, patients should be adequately hydrated before and after amifostine administration to reduce the risk of hypotension, a common side effect. Close monitoring of blood pressure during treatment is essential, especially in patients with a history of cardiovascular disease or those prone to hypotension.

Additionally, caution should be exercised when administering amifostine to patients with a history of seizures, as the drug may lower the seizure threshold. Electrolyte levels, including calcium, magnesium, and potassium, should be monitored regularly during treatment, as amifostine can cause electrolyte imbalances, which may manifest as muscle cramps, weakness, or irregular heartbeat.

Patients should be informed about the signs and symptoms of allergic reactions, such as rash, itching, swelling, or difficulty breathing, and instructed to seek immediate medical attention if they occur. 

Overall, careful monitoring and appropriate precautions can help mitigate the risks associated with amifostine therapy and ensure the safe and effective use of this medication in cancer treatment.

Amifostine may interact with certain chemotherapy medications, affecting their metabolism or efficacy. Close monitoring is necessary when administering amifostine alongside chemotherapy to ensure optimal treatment outcomes.

Concomitant use of amifostine with blood pressure-lowering medications may potentiate hypotensive effects, leading to a further decrease in blood pressure. Adjustments to the dosage of antihypertensive drugs may be required to prevent excessive hypotension.

Although not a drug interaction in the traditional sense, amifostine’s cytoprotective effects during radiation therapy may influence treatment outcomes and radiation dose delivery. Healthcare providers should consider the timing and dosage of amifostine administration in relation to radiation therapy sessions to optimize therapeutic benefits.

Patients should inform their healthcare providers about all medications they are taking, including prescription, over-the-counter, and herbal supplements, to minimize the risk of drug interactions. Close monitoring and appropriate dosage adjustments may be necessary when combining amifostine with other medications to ensure patient safety and treatment efficacy.

Amifostine dosage guidelines vary depending on the specific indication and patient factors. For chemotherapy-induced nausea and vomiting (CINV), the typical intravenous dose is 910 mg/m² administered before chemotherapy sessions. 

This infusion is usually completed approximately 15-30 minutes prior to initiating chemotherapy to maximize its cytoprotective effects. In cases of radiation-induced xerostomia during head and neck cancer treatment, amifostine is given intravenously at a dose of 200 mg/m² once daily, also administered 15-30 minutes before radiation therapy. 

Dose adjustments may be necessary for patients with renal impairment to minimize the risk of toxicity. Proper reconstitution and administration techniques are crucial to ensure the drug’s efficacy and safety. 

Regular monitoring of blood pressure, renal function, and electrolyte levels is recommended throughout the treatment course. Adherence to the prescribed dosing schedule and close communication with healthcare providers are essential for optimizing treatment outcomes and minimizing adverse effects associated with amifostine therapy.

• Amifostine is available by prescription only.
• It should be obtained from a licensed pharmacy with a valid prescription.
• Administration should be supervised by a qualified healthcare professional experienced in chemotherapy or radiation therapy.
• Patients should follow dosage and administration instructions provided by their healthcare provider closely.
• Regular follow-up appointments with the prescribing physician are essential for monitoring treatment efficacy and safety.
• Patients should not use amifostine without proper medical guidance and assessment of their medical history and current condition.

1. What is Amifostine?

Amifostine is a cytoprotective agent primarily used as a protective treatment for certain types of chemotherapy and radiation therapy. It helps to reduce the risk of damage to normal tissues during cancer treatment.

2. How does Amifostine work?

Amifostine acts as a free radical scavenger, protecting healthy cells from the oxidative stress caused by chemotherapy and radiation. It converts to an active form that neutralizes harmful free radicals.

3. What are the common uses of Amifostine?

Amifostine is commonly used to prevent kidney damage from cisplatin chemotherapy and to protect against xerostomia (dry mouth) caused by radiation therapy in head and neck cancer.

4. What are the side effects of Amifostine?

Common side effects may include hypotension (low blood pressure), nausea, vomiting, dizziness, and allergic reactions. More severe effects can include anaphylaxis and electrolyte imbalances.

5. How is Amifostine administered?

Amifostine is typically administered via intravenous infusion. It’s usually given just before chemotherapy or radiation treatments.

6. Who should not use Amifostine?

Amifostine is contraindicated in patients with known hypersensitivity to the drug, those with severe renal impairment, or those who are dehydrated.

7. Can Amifostine be used in pediatric patients?

While Amifostine is used primarily in adults, its safety and efficacy in pediatric patients have not been thoroughly studied, so use in children is generally approached with caution.

8. How quickly does Amifostine start working?

Amifostine typically begins to exert its protective effects shortly after administration. Clinicians generally administer it about 30 minutes before chemotherapy or radiation.

9. Are there any drug interactions with Amifostine?

Amifostine may interact with certain medications, including other chemotherapeutic agents. It’s crucial to inform your healthcare provider about all medications being taken.

10. What monitoring is required while on Amifostine?

Patients receiving Amifostine should be monitored for blood pressure, renal function, and any signs of allergic reactions, particularly after the first dose.

11. Can I drink alcohol while taking Amifostine?

It’s advisable to avoid alcohol while taking Amifostine, as it may exacerbate side effects and increase the risk of dehydration or hypotension.

12. Is Amifostine effective against all types of cancers?

Amifostine is not effective against all types of cancers. Its use is specific to particular cancers and therapy regimens, especially those involving cisplatin or radiation.

13. Does Amifostine affect chemotherapy effectiveness?

Amifostine is designed to protect healthy tissues without significantly affecting the efficacy of chemotherapy. Studies indicate it does not compromise tumor response to treatment.

14. Can Amifostine cause allergic reactions?

Yes, Amifostine can cause allergic reactions in some patients, ranging from mild to severe (anaphylactic reactions). Patients should be monitored for any signs of an allergic response during infusion.

15. Is it safe to use Amifostine during pregnancy?

Amifostine should be used during pregnancy only if the potential benefits outweigh the risks, and it should be discussed with a healthcare provider.

16. Can Amifostine cause dehydration?

Yes, Amifostine can lead to dehydration, particularly if not properly hydrated prior to administration. Patients are often encouraged to drink fluids before treatment.

17. What is the correct dosage of Amifostine?

The dosage of Amifostine can vary based on the indication and patient conditions, but a common regimen is 910 mg/m² administered intravenously before chemotherapy.

18. How long is Amifostine treatment typically administered?

The duration of Amifostine treatment depends on the treatment protocol but is generally administered just before chemotherapy sessions.

19. Are there any long-term effects of Amifostine use?

Long-term effects of Amifostine are not extensively studied, but most side effects are short-term and resolve after treatment. Ongoing assessment is necessary for any chronic conditions.

20. How should Amifostine be stored?

Amifostine should be stored at room temperature, protected from light. Reconstituted solutions should be used immediately or stored as directed by the healthcare provider.