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  • Pages
  • Editions
01 Welcome
02 Introduction
03 #1 DEP and AI
04 #2 Radiogligand
05 #3 Living Cancer Cell Liquid
06 #4 Solid Tumor
07 #5 AI Driven SaaS
08 #6 Nanoparticles Reprogram
09 #7 Dual Checkpoint
10 #8 Approved HER2
11 #9 Biosimilar
12 #10 Big Data

#7 Dual Checkpoint Inhibitor Improves Anti-Tumor Response

Oncology Advancements: Top 10 of 2022

The combination of two immune checkpoint inhibitors for the treatment of advanced melanomas was approved by the FDA[2].

Why is this significant?

This approval introduces a new combination of immunotherapies that may act together to improve the anti-tumor response. This demonstrates the possibility of targeting two or maybe more different immune checkpoints.

Why Could this Impact Care?

This approval not only adds another weapon against melanoma, but it officially validates LAG-3 as a clinically effective checkpoint inhibitor. This is the first checkpoint inhibitor approved since Keytruda in 2014. The combination of two checkpoint inhibitors met the primary end point of progression-free survival (PFS) in first line treatment of metastatic or unresectable melanoma. When the combination was compared to one checkpoint inhibitor alone, PFS was extended from 4.6 months to 10.1 months[1].

Opdualag™ (new therapy) consist of a new checkpoint inhibitor, relatlimab, which blocks the LAG-3 protein found on immune cells. This is then paired with nivolumab which blocks a different immune checkpoint protein (PD-1).

Together these drugs promote an immune response against advanced or difficult to remove tumors.

Sources:

Bristol Myers Squibb announced the FDA approval of Opdualag (nivolumab/relatlimab-rmbw), for the treatment of adult and pediatric patients 12 years of age or older with unresectable or metastatic melanoma.

1. Relatlimab and Nivolumab versus Nivolumab in Untreated Advanced Melanoma
2. Opdualag Becomes First FDA-Approved Immunotherapy to Target LAG-3