| Liver carcinoma

Lenvima vs Keytruda

Side-by-side clinical, coverage, and cost comparison for liver carcinoma.
Deep comparison between: Lenvima vs Keytruda with Prescriber.AI
AI compares prescribing info and payer-specific access barriers across 1,200+ formularies. Here's a preview of what prescribers are already asking.
Safety signalsKeytruda has a higher rate of injection site reactions vs Lenvima based on FDA-approved prescribing information
Coverage gaps3 major payers require step therapy for Keytruda but not Lenvima, including UnitedHealthcare
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Lenvima
Keytruda
At A Glance
Oral
Once daily
Multi-kinase inhibitor
IV infusion
Every 3 weeks or Every 6 weeks
PD-1 inhibitor
Indications
  • Differentiated Thyroid Gland Carcinoma
  • Renal Cell Carcinoma
  • Liver carcinoma
  • Endometrial Carcinoma
  • melanoma
  • Non-Small Cell Lung Carcinoma
  • Malignant Pleural Mesothelioma
  • Squamous cell carcinoma of the head and neck
  • Classic Hodgkin Lymphoma
  • Mediastinal (Thymic) Large B-Cell Lymphoma
  • Urothelial Carcinoma
  • Colorectal Carcinoma
  • Stomach Carcinoma
  • Esophageal carcinoma
  • Cervix carcinoma
  • Liver carcinoma
  • Biliary Tract Cancer
  • Merkel cell carcinoma
  • Renal Cell Carcinoma
  • Endometrial Carcinoma
  • Triple-Negative Breast Carcinoma
  • Malignant neoplasm of ovary
  • Squamous cell carcinoma of skin
Dosing
Differentiated Thyroid Gland Carcinoma 24 mg orally once daily until disease progression or unacceptable toxicity.
Renal Cell Carcinoma (first-line, with pembrolizumab) 20 mg orally once daily in combination with pembrolizumab 200 mg IV infusion over 30 minutes every 3 weeks until disease progression or unacceptable toxicity or up to 2 years.
Renal Cell Carcinoma (previously treated, with everolimus) 18 mg orally once daily in combination with everolimus 5 mg orally once daily until disease progression or unacceptable toxicity.
Liver carcinoma 12 mg orally once daily for patients >=60 kg or 8 mg orally once daily for patients <60 kg, until disease progression or unacceptable toxicity.
Endometrial Carcinoma 20 mg orally once daily in combination with pembrolizumab 200 mg IV infusion over 30 minutes every 3 weeks until unacceptable toxicity or disease progression.
melanoma 200 mg every 3 weeks or 400 mg every 6 weeks IV; 2 mg/kg (up to 200 mg) every 3 weeks IV for pediatrics
Non-Small Cell Lung Carcinoma 200 mg every 3 weeks or 400 mg every 6 weeks IV
Malignant Pleural Mesothelioma 200 mg every 3 weeks or 400 mg every 6 weeks IV
Squamous cell carcinoma of the head and neck 200 mg every 3 weeks or 400 mg every 6 weeks IV
Classic Hodgkin Lymphoma 200 mg every 3 weeks or 400 mg every 6 weeks IV for adults; 2 mg/kg (up to 200 mg) every 3 weeks IV for pediatrics
Mediastinal (Thymic) Large B-Cell Lymphoma 200 mg every 3 weeks or 400 mg every 6 weeks IV for adults; 2 mg/kg (up to 200 mg) every 3 weeks IV for pediatrics
Urothelial Carcinoma 200 mg every 3 weeks or 400 mg every 6 weeks IV
Colorectal Carcinoma 200 mg every 3 weeks or 400 mg every 6 weeks IV for adults; 2 mg/kg (up to 200 mg) every 3 weeks IV for pediatrics
Stomach Carcinoma 200 mg every 3 weeks or 400 mg every 6 weeks IV
Esophageal carcinoma 200 mg every 3 weeks or 400 mg every 6 weeks IV
Cervix carcinoma 200 mg every 3 weeks or 400 mg every 6 weeks IV
Liver carcinoma 200 mg every 3 weeks or 400 mg every 6 weeks IV
Biliary Tract Cancer 200 mg every 3 weeks or 400 mg every 6 weeks IV
Merkel cell carcinoma 200 mg every 3 weeks or 400 mg every 6 weeks IV for adults; 2 mg/kg (up to 200 mg) every 3 weeks IV for pediatrics
Renal Cell Carcinoma 200 mg every 3 weeks or 400 mg every 6 weeks IV as single agent or in combination with axitinib 5 mg orally twice daily or lenvatinib 20 mg orally once daily
Endometrial Carcinoma 200 mg every 3 weeks or 400 mg every 6 weeks IV in combination with carboplatin and paclitaxel, or with lenvatinib 20 mg orally once daily, or as single agent for MSI-H or dMMR tumors
Triple-Negative Breast Carcinoma 200 mg every 3 weeks or 400 mg every 6 weeks IV
Malignant neoplasm of ovary 200 mg every 3 weeks or 400 mg every 6 weeks IV
Squamous cell carcinoma of skin 200 mg every 3 weeks or 400 mg every 6 weeks IV
Contraindications
    Adverse Reactions
    Most common (>=20%) Hypertension, fatigue, diarrhea, arthralgia/myalgia, decreased appetite, decreased weight, nausea, stomatitis, headache, vomiting, proteinuria, palmar-plantar erythrodysesthesia syndrome, abdominal pain, dysphonia, hypothyroidism, hemorrhagic events, rash, musculoskeletal pain.
    Serious Hepatic encephalopathy, hepatic failure, cardio-respiratory arrest, sepsis, myocardial infarction, pneumonitis, acute kidney injury, renal failure, dehydration, thrombocytopenia, dyspnea, anemia.
    Postmarketing Pancreatitis, impaired wound healing, cholecystitis, nephrotic syndrome, arterial aneurysms/dissections/rupture.
    Most common (>=20%) fatigue, musculoskeletal pain, decreased appetite, rash, diarrhea, nausea, cough, dyspnea, constipation, pruritus, hypothyroidism
    Serious pneumonitis, colitis, hepatitis, endocrinopathies, nephritis with renal dysfunction, dermatologic adverse reactions, myocarditis, neurological toxicities, infusion-related reactions, immune-mediated adverse reactions
    Postmarketing exocrine pancreatic insufficiency, sclerosing cholangitis
    Pharmacology
    Lenvatinib is a multi-kinase inhibitor that inhibits VEGFR1, VEGFR2, and VEGFR3 kinase activities as well as FGFR1-4, PDGFRA, KIT, and RET, suppressing pathogenic angiogenesis and tumor growth; in combination with pembrolizumab or everolimus, it demonstrates enhanced antiangiogenic and antitumor activity.
    Pembrolizumab is a PD-1 blocking antibody that releases PD-1 pathway-mediated inhibition of the immune response by preventing the interaction of PD-1 with its ligands PD-L1 and PD-L2, thereby restoring anti-tumor immune response.
    Enter your patient's insuranceCheck specific coverage details for your patient.
    Most Common Insurance
    Anthem BCBS
    Lenvima
    • Covered on 5 commercial plans
    • PA (11/12) · Step Therapy (0/12) · Qty limit (11/12)
    View full coverage details ›
    Keytruda
    • Covered on 5 commercial plans
    • PA (12/12) · Step Therapy (0/12) · Qty limit (0/12)
    View full coverage details ›
    UnitedHealthcare
    Lenvima
    • Covered on 4 commercial plans
    • PA (8/8) · Step Therapy (0/8) · Qty limit (4/8)
    View full coverage details ›
    Keytruda
    • Covered on 4 commercial plans
    • PA (0/8) · Step Therapy (0/8) · Qty limit (0/8)
    View full coverage details ›
    Humana
    Lenvima
    • Covered on 0 commercial plans
    • PA (3/3) · Step Therapy (2/3) · Qty limit (2/3)
    View full coverage details ›
    Keytruda
    • Covered on 0 commercial plans
    • PA (3/3) · Step Therapy (0/3) · Qty limit (2/3)
    View full coverage details ›
    Coverage data sourced from MMIT. Updated monthly.
    Savings
    No savings programs available for Lenvima.
    No savings programs available for Keytruda.
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    LenvimaView full Lenvima profile
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    Clinical data sourced from FDA-approved labeling. Coverage data via MMIT. Updated monthly.