Lenalidomide
Lenalidomide.JPG

Lenalidomide

CLINICAL USE

Treatment of multiple myeloma in combination with dexamethasone

DOSE IN NORMAL RENAL FUNCTION

25 mg daily on days 1–21 of a 28 day cycle; reduce dose if patient has neutropenia or thrombocytopenia; see data sheet

PHARMACOKINETICS

  • Molecular weight                           :259.3
  • %Protein binding                           :22.7–29.2
  • %Excreted unchanged in urine     : 65–85
  • Volume of distribution (L/kg)       :86 litres
  • half-life – normal/ESRD (hrs)      :3.5/>9

    DOSE IN RENAL IMPAIRMENT

    GFR (mL/MIN)

    30–50 10 mg daily, increasing to 15 mg after 2 cycles if patient is not responding<30 15 mg every 48 hours

    DOSE IN PATIENTS UNDERGOING RENAL REPLACEMENT THERAPIES

  • CAPD                :Probably dialysed. 15 mg 2–3 times a week
  • HD                     :Probably dialysed. 15 mg 3 times a week post dialysis
  • HDF/high flux   :Probably dialysed. 15 mg 3 times a week post dialysis
  • CAV/VVHD      :Probably dialysed. Dose as in GFR=30–50 mL/min

    IMPORTANT DRUG INTERACTIONS

    Potentially hazardous interactions with other drugsCardiac glycosides: possibly increases concentration of digoxin

    ADMINISTRATION

    Reconstition

    Route

    Oral

    Rate of Administration

    Comments

    OTHER INFORMATION

    May cause acute renal failure – monitor renal function during treatment. Patients with renal impairment are more likely to develop side effects



    See how to identify renal failure stages according to GFR calculation

    See how to diagnose irreversible renal disease

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