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pazopani

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In China, pazopanib was approved for marketing on March 3, 2017; the National Medical Products Administration (NMPA) approved pazopanib for the first-line treatment of patients with advanced renal cell carcinoma and patients with advanced renal cancer who have received cytokine therapy.

1. Drug name

1. Generic name: pazopanib (pazopanib)

2. Trade name: VOTRIENT

2. Indications

It is used to treat patients with advanced renal cell carcinoma (RCC).

3. Specifications and properties

200mg, tablet.

IV. Usage and Dosage

1. Recommended dose: 800mg orally, once a day.

2. Taking time: Take on an empty stomach (1 hour before meals or 2 hours after meals).

3. Do not crush it for consumption (it may increase the absorption rate and affect the efficacy).

5. Dose adjustment

1. Hepatic insufficiency : reduce to 200mg/day for patients with moderate liver function impairment; contraindicated for patients with severe liver function impairment.

2. Drug interaction :

When strong CYP3A4 inhibitors (such as ketoconazole) are used together, reduce the dose to 400mg.

Concomitant use of strong CYP3A4 inducers (such as rifampicin) should be avoided.

3. Other adjustments : Adjust in steps of 200mg based on tolerance, with the maximum dose not exceeding 800mg.

6. Precautions for medication

1. Effect of diet : High-fat/low-fat diet will increase the blood concentration of the drug by 2 times, and it must be taken on an empty stomach.

2. Treatment of missed doses : If it is less than 12 hours before the next dose, skip it and do not take it again.

3. Vomiting treatment : If you vomit after taking the medicine, do not take more medicine. Take the medicine next time as originally planned.

4. before and after surgery: Stop medication for at least 7 days before surgery. The time to resume medication after surgery will be determined based on the wound healing condition.

7. Medication for special groups

1. Pregnant women : It can cause fetal damage and is contraindicated during pregnancy (pregnancy grade D).

2. Lactation : Suspend breastfeeding (it is unknown whether the drug enters the breast).

3. Children : safety has not been established.

4. Elderly : Patients aged ≥65 years old need to monitor liver function more closely.

8. Adverse reactions

1. Common (≥20%) : diarrhea, hypertension, hair discoloration, nausea, anorexia, vomiting.

2. Serious adverse reactions :

Hepatotoxicity (monitor ALT/AST), QT interval prolongation (monitor electrocardiogram), bleeding events (disabled for those with a history of bleeding within 6 months), arterial thrombosis (risk of myocardial infarction/stroke).

9. Contraindications

There are no absolute contraindications, but it is prohibited in the following situations:

1. Severe liver function damage.

2. History of cerebral hemorrhage/digestive tract bleeding within 6 months.

3. Pregnancy period.

10. Drug interactions

1. CYP3A4 inhibitor : Avoid combined use of strong inhibitors (such as clarithromycin).

2. CYP3A4 inducer : Avoid combined use of strong inducers (such as rifampicin).

3. Narrow therapeutic window drug : Avoid combined use of drugs metabolized by CYP3A4/2D6/2C8 (such as warfarin).

11. Storage method

It is not clearly stated. It is recommended to store it according to the conventional oral tablets (avoid light, in a cool and dry place).