Opdivo (Nivolumab) vs Lenvima (lenvatinib)

Opdivo (Nivolumab) vs Lenvima (lenvatinib)

Opdivo (nivolumab) is an immune checkpoint inhibitor that works by enhancing the body's immune response against cancer cells, and is commonly used in various types of cancers, including melanoma, lung, and kidney cancers. Lenvima (lenvatinib) is a tyrosine kinase inhibitor that targets specific enzymes involved in the growth and spread of cancer cells, and is often used for treating thyroid cancer and in combination with other drugs for kidney and endometrial cancers. The choice between Opdivo and Lenvima would depend on the specific type of cancer, its stage, the patient's overall health, and the treatment goals, as these medications have different mechanisms of action and side effect profiles.

Difference between Opdivo and Lenvima

Metric Opdivo (Nivolumab) Lenvima (lenvatinib)
Generic name Nivolumab Lenvatinib
Indications Various types of cancer including melanoma, lung cancer, renal cell carcinoma, Hodgkin lymphoma, head and neck cancer, urothelial carcinoma, and colorectal cancer Thyroid cancer, renal cell carcinoma, hepatocellular carcinoma, and in combination with other drugs for endometrial carcinoma
Mechanism of action PD-1 immune checkpoint inhibitor that blocks the interaction between PD-1 and its ligands, PD-L1 and PD-L2 Multikinase inhibitor that targets vascular endothelial growth factor (VEGF) receptors, fibroblast growth factor (FGF) receptors, platelet-derived growth factor (PDGF) receptor alpha, RET, and KIT
Brand names Opdivo Lenvima
Administrative route Intravenous infusion Oral
Side effects Fatigue, rash, musculoskeletal pain, pruritus, diarrhea, nausea, and others Hypertension, fatigue, diarrhea, decreased appetite, weight loss, and others
Contraindications Known hypersensitivity to nivolumab or any of its excipients Known hypersensitivity to lenvatinib or any of its excipients
Drug class Immune checkpoint inhibitor Tyrosine kinase inhibitor
Manufacturer Bristol-Myers Squibb Eisai Co., Ltd.

Efficacy

Overview of Opdivo (Nivolumab) and Lenvima (Lenvatinib) in Liver Cancer

Opdivo (nivolumab) and Lenvima (lenvatinib) are two medications that have shown efficacy in the treatment of liver cancer, specifically hepatocellular carcinoma (HCC), which is the most common type of liver cancer. Opdivo is an immune checkpoint inhibitor that works by blocking the PD-1 pathway, which cancer cells often exploit to evade the immune system. Lenvima, on the other hand, is a multikinase inhibitor that targets the vascular endothelial growth factor (VEGF) receptors, among other kinases, and is involved in angiogenesis, the process by which tumors develop their own blood supply.

Efficacy of Lenvima (Lenvatinib) as a First-Line Treatment

Lenvima has been approved as a first-line treatment for unresectable hepatocellular carcinoma. In a pivotal phase 3 clinical trial known as the REFLECT study, lenvatinib demonstrated non-inferiority to the standard-of-care sorafenib in terms of overall survival. Additionally, lenvatinib showed statistically significant improvements in progression-free survival (PFS) and a higher objective response rate (ORR) compared to sorafenib, suggesting that lenvatinib may offer some benefits over the existing first-line treatment for HCC.

Efficacy of Opdivo (Nivolumab) as a Second-Line Treatment

Opdivo has been evaluated as a second-line treatment for patients with hepatocellular carcinoma who have previously been treated with sorafenib. The CheckMate 040 trial, a phase 1/2 study, indicated that nivolumab had a manageable safety profile and provided durable responses in a subset of patients with advanced HCC. The overall response rate and the duration of response observed in the trial supported the potential of nivolumab as a treatment option for HCC after prior sorafenib therapy.

Combination Therapy in Advanced HCC

More recently, the combination of Opdivo and Lenvima has been explored as a treatment for advanced HCC. The CheckMate 459 study, a phase 3 trial, investigated the combination of nivolumab plus lenvatinib versus sorafenib. While the study did not meet its primary endpoint of improving overall survival compared to sorafenib, the combination therapy did show an improvement in progression-free survival and objective response rate. These findings suggest that the combination of nivolumab and lenvatinib may offer a potential therapeutic strategy for patients with advanced HCC, although further research is needed to fully understand the benefits and optimal use of this combination.

Regulatory Agency Approvals

Opdivo
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA
  • Health Canada
  • Pharmaceuticals and Medical Devices Agency (PMDA), Japan
  • Therapeutic Goods Administration (TGA), Australia
  • Medsafe (NZ)
Lenvima
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA
  • Health Canada
  • Pharmaceuticals and Medical Devices Agency (PMDA), Japan
  • Therapeutic Goods Administration (TGA), Australia

Access Opdivo or Lenvima today

If Opdivo or Lenvima are not approved or available in your country (e.g. due to supply issues), you can access them via Everyone.org.

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