Jakafi

Clinical Notes

Jakafi (ruxolitinib) is a JAK1/JAK2 inhibitor used for myeloproliferative neoplasms and graft-versus-host disease.

Indication Intermediate or high-risk myelofibrosis; polycythemia vera inadequately controlled by hydroxyurea; steroid-refractory acute and chronic graft-versus-host disease (GVHD)
Mechanism of Action Inhibits Janus kinases JAK1 and JAK2, blocking JAK-STAT signaling pathway that is dysregulated in myeloproliferative neoplasms and GVHD inflammatory responses
Pharmacokinetics Bioavailability ~95%; peak 1-2 hours; half-life 3-5 hours; 97% protein bound; hepatic metabolism via CYP3A4 (major), CYP2C9; renal excretion (74%); active metabolites contribute to effect
Dosing Myelofibrosis: Based on platelet count—20 mg BID if >200K, 15 mg BID if 100-200K, 5 mg BID if 50-100K; PV: 10 mg BID; GVHD: 5-10 mg BID; adjust for renal/hepatic impairment and CYP3A4 interactions
Contraindications No absolute contraindications; use with caution in severe renal or hepatic impairment, active infections
Adverse Effects Thrombocytopenia, anemia, neutropenia, infections (including opportunistic—TB, PML, hepatitis B reactivation), bruising, dizziness, headache, non-melanoma skin cancer, weight gain
Drug Interactions Strong CYP3A4 inhibitors (ketoconazole) increase levels—reduce dose by 50%; fluconazole requires dose reduction; strong CYP3A4 inducers decrease levels—may need dose increase
Monitoring CBC with differential at baseline, every 2-4 weeks until stable, then as indicated; LFTs; renal function; screen for TB and hepatitis B before starting; signs of infection
Other Considerations Do not abruptly discontinue (may cause return of symptoms/cytokine storm); taper over 1-2 weeks; can be given with or without food; reduces spleen size and constitutional symptoms
Reference Jakafi prescribing information; COMFORT trials; REACH trials

Quick-reference tip: Jakafi targets JAK1/2—”JAK-afi” shrinks spleens in myelofibrosis and controls GVHD; watch blood counts closely.

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