• Drug class: Second-generation proteasome inhibitor.
  • Mechanism of action:
    • Irreversibly binds to the 20S proteasome (chymotrypsin-like activity).
    • Inhibits degradation of ubiquitinated proteins → protein accumulation → apoptosis of malignant plasma cells.

Indications (FDA/EMA approved):

Dosing (IV only):

  • Dose depends on regimen:
    • Once weekly dosing: 70 mg/m² IV over 30 min, Days 1, 8, 15 of 28-day cycle.
    • Twice weekly dosing: 20 mg/m² IV Day 1, then escalate to 27–56 mg/m² IV over 10–30 min on Days 1, 2, 8, 9, 15, 16 of 28-day cycle.
  • Pre- and post-hydration recommended to reduce risk of renal/cardiac toxicity.
  • Dexamethasone premedication (to reduce infusion reaction).

Key adverse effects:

  • Cardiac toxicity: Heart failure, ischemia, arrhythmias, hypertension.
  • Pulmonary: Dyspnea, pulmonary hypertension.
  • Hematologic: Thrombocytopenia, anemia, neutropenia.
  • Renal toxicity: AKI (especially early cycles).
  • Infusion-related reactions.
  • Other: Fatigue, diarrhea, fever.

Pharmacist notes / Monitoring:

  • Cardiac monitoring: Assess baseline cardiac history, monitor BP, EF if high risk.
  • Renal function: Check before each cycle, adjust dose for toxicity (not strictly for baseline CrCl).
  • CBC: Monitor for cytopenias.
  • Hydration: 250–500 mL IV before dose (caution in CHF).
  • Antiviral prophylaxis (e.g., acyclovir) recommended for herpes zoster prevention.

Exam/clinical highlights:

  • Target: 20S proteasome (irreversible inhibitor).
  • Use: Relapsed/refractory MM in multiple combinations.
  • Toxicities: Cardiac (HF, HTN), renal, cytopenias → distinguish from bortezomib (neuropathy).
  • Supportive care: Hydration, dex premedication, antiviral prophylaxis.