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REVLIMID is indicated for the treatment of adult patients with mantle cell lymphoma (MCL) whose disease has relapsed or progressed after two prior therapies, one of which included bortezomib. REVLIMID is not indicated and is not recommended for the treatment of patients with chronic lymphocytic leukemia (CLL) outside of controlled clinical trials.
REVLIMID is an oral agent approved for use in relapsed or refractory MCL1*
*Patients must have received prior bortezomib.
Available in 5 dosage strengths
REVLIMID is available in 5-mg, 10-mg, 15-mg, 20-mg, and 25-mg capsules. The recommended starting dose for relapsed or refractory MCL is 25 mg/day orally on Days 1-21 of repeated 28-day cycles. Treatment should be continued until disease progression or unacceptable toxicity. For recommended starting dose adjustments in moderate to severe renal impairment, as well as end-stage renal disease, please click here.
Capsules shown are not actual size.
Important Dosing Information
- The capsules should not be opened, broken, or chewed
- REVLIMID is primarily excreted unchanged by the kidney. Since elderly patients are more likely to have decreased renal function, care should be taken in dose selection. Monitor renal function
- Monitor CBCs weekly for the first cycle (28 days), every 2 weeks during cycles 2-4, then monthly thereafter
- Treatment is continued or modified based on clinical and laboratory findings
- Dose modification guidelines are recommended to manage Grade 3/4 neutropenia or thrombocytopenia. For non-hematologic Grade 3/4 toxicities judged to be related to REVLIMID, hold treatment and restart at next lower dose level when toxicity has resolved to ≤Grade 2
- For Grade 3 or 4 tumor flare reaction (TFR), recommended to withhold treatment with REVLIMID until TFR resolves to ≤Grade 1
- Patients may require dose interruption and/or reduction
- Patients may require the use of blood product support and/or growth factors
REVLIMID offers refractory or relapsed MCL patients once-daily oral dosing.1
Explore Dosing Schedule
