Informational only — Not medical advice. Always consult a licensed healthcare provider.

Community data Updated 23 hours ago

Indications

Carfilzomib is a proteasome inhibitor. It is used in adults with relapsed or refractory multiple myeloma who have received one to three lines of therapy, and in this group it is given in combination with one of the following: Lenalidomide and dexamethasone, or Dexamethasone alone, or Daratumumab and dexamethasone, or Daratumumab and hyaluronidase-fihj and dexamethasone, or Isatuximab and dexamethasone. Carfilzomib can also be used as a single agent in patients with relapsed or refractory multiple myeloma who have received one or more lines of therapy.

⚠️ Always consult a registered physician before taking any medicine.

Pharmacology

Carfilzomib is a tetrapeptide epoxyketone proteasome inhibitor. It binds irreversibly to the N-terminal threonine-containing active sites of the 20S proteasome, which is the proteolytic core particle inside the 26S proteasome. In laboratory (in vitro) studies, carfilzomib had antiproliferative and proapoptotic activities in solid and hematologic tumor cells. In animals, it inhibited proteasome activity in blood and tissue, and it delayed tumor growth in models of multiple myeloma, hematologic tumors and solid tumors.

Pregnancy & Breastfeeding

Carfilzomib can harm an unborn baby. This is based on findings from animal studies and on how the medicine works. There are no data on the use of carfilzomib in pregnant women, so the risk linked to the drug can't be properly assessed. In rabbits, carfilzomib caused embryo-fetal lethality at doses lower than the clinical dose. Pregnant women should be told about the potential risk to the fetus.

There are also no data on whether carfilzomib passes into human milk, what effect it has on a breastfed child, or whether it changes milk production. Because the breastfed child could have serious adverse reactions, women are advised not to breastfeed during treatment with carfilzomib and for 2 weeks after treatment.

⚠️ Talk to your doctor before taking any medicine during pregnancy or while breastfeeding.

Dosage Reference

⚠️ Reference ranges from official sources only. Consult your doctor for personalized dosing.

Adults: Hydration: Make sure the patient is well hydrated before Carfilzomib is given in Cycle 1, especially when there is a high risk of tumor lysis syndrome (TLS) or renal toxicity. Consider both oral fluids (30 mL per kg at least 48 hours before Cycle 1, Day 1) and intravenous fluids (250 mL to 500 mL of a suitable intravenous fluid before each dose in Cycle 1). If needed, give another 250 mL to 500 mL of intravenous fluids after the dose. In later cycles, continue oral and/or intravenous hydration as needed. Watch the patient for signs of volume overload and adjust the fluids to what each patient needs, particularly in those with cardiac failure or at risk of it. Premedications and Concomitant Medications: Give the recommended dose of dexamethasone, whether it is for monotherapy or as part of the combination therapy. Give it orally or intravenously at least 30 minutes but no more than 4 hours before every dose of Carfilzomib in Cycle 1, to reduce how often infusion-related reactions occur and how severe they are. If these symptoms occur in later cycles, start the dexamethasone premedication again. Provide thromboprophylaxis for patients who receive Carfilzomib together with other therapies. Consider antiviral prophylaxis to lower the risk of herpes zoster reactivation. Electrolyte Monitoring: Check serum potassium levels regularly during treatment.

Side Effects & Interactions

Side Effects

No side-effect data recorded yet.

Key Interactions

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