mosunetuzumab-axgb (Lunsumio)

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Indications

Contraindications

Dosage

  • administer 8 cycles
    • unless complete response, an additional 9 cycles of treatment (17 cycles total)
  • premedicate to reduce risk of cytokine release syndrome & infusion-related reaction
  • cycle 1 day 1: 1 mg
  • cycle 1 day 8: 2 mg
  • cycle 1 day 15: 60 mg
  • cycle 2 day 1: 60 mg
  • cycle 3+ day 1: 30 mg

* a treatment cycle is 21 days

* cycle 1: administer over minimum of 4 hours

* subsequent cycles: administer over minimum of 2 hours if cycle 1 well tolerated

* premedicate with dexamethasone 20 mg or methylprednisolone 80 mg IV, diphenhydramine 50-100 mg, acetaminophen 500-1000 mg 30 minutes prior to infusion (all patients cycles 1 & 2), & subsequent cycles for patients who experienced cytokine release syndrome during cycles 1 & 2.

1 mg/mL: 1 mL, 30 mL

Adverse effects

Mechanism of action

More general terms

References

  1. Food and Drug Administration (FDA) December 22, 2022 FDA grants accelerated approval to mosunetuzumab-axgb for relapsed or refractory follicular lymphoma. https://www.fda.gov/drugs/resources-information-approved-drugs/fda-grants-accelerated-approval-mosunetuzumab-axgb-relapsed-or-refractory-follicular-lymphoma
  2. HIGHLIGHTS OF PRESCRIBING INFORMATIO Lunsumio <TM> (mosunetuzumab-axgb) injection, for intravenous https://www.accessdata.fda.gov/drugsatfda_docs/label/2022/761263s000lbl.pdf