The recommended dosage of Sunitinib for gastrointestinal stromal tumor (GIST) and advanced renal cell carcinoma (RCC) is 50 mg taken orally once daily, on a schedule of 4 weeks on treatment followed by 2 weeks off (Schedule 4/2) until disease progression or unacceptable toxicity. Sunitinib may be taken with or without food.
The recommended dosage of Sunitinib for the adjuvant treatment of RCC is 50 mg taken orally once daily, on a schedule of 4 weeks on treatment followed by 2 weeks off (Schedule 4/2), for nine 6-week cycles. Sunitinib may be taken with or without food.
The recommended dosage of Sunitinib for pancreatic neuroendocrine tumors (pNET) is 37.5 mg taken orally once daily until disease progression or unacceptable toxicity. Sunitinib may be taken with or without food.
To manage adverse reactions, the recommended dosage modifications are provided in Table 1. Table 2 provides the recommended dosage reductions of Sunitinib for adverse reactions.
Select an alternate concomitant medication with no or minimal enzyme inhibition potential. If coadministration of Sunitinib with a strong CYP3A4 inhibitor cannot be avoided, consider a dose reduction for Sunitinib to a minimum dosage as follows:
• GIST and RCC: 37.5 mg orally once daily, on a schedule of 4 weeks on treatment followed by 2 weeks off (Schedule 4/2)
• pNET: 25 mg orally once daily
Select an alternate concomitant medication with no or minimal enzyme induction potential. If coadministration of Sunitinib with a strong CYP3A4 inducer cannot be avoided, consider a dose increase for Sunitinib to a maximum dosage as follows:
• GIST and RCC: 87.5 mg orally once daily, on a schedule of 4 weeks on treatment followed by 2 weeks off (Schedule 4/2)
• pNET: 62.5 mg orally once daily If the dose of Sunitinib is increased, monitor patients carefully for adverse reactions.
No starting dose adjustment is required in patients with end-stage renal disease (ESRD) on hemodialysis. However, given the decreased exposure compared to patients with normal renal function, subsequent doses may be increased gradually up to 2-fold based on safety and tolerability.
from FDA,2021.08