Drug intelligence / Profile preview

atezolizumab + oxaliplatin + leucovorin + 5-fluorouracil

Development stage
Unknown
Lead developer
Genentech
Modality
Monoclonal Antibodies → Antibody-Based Therapeutics, Small Molecules
Administration
Intravenous
01

Overview

Atezolizumab + oxaliplatin + leucovorin + 5-fluorouracil is a four-drug combination regimen studied as an adjuvant therapy for stage III colon cancer with deficient DNA mismatch repair (dMMR) or microsatellite instability (MSI). **Atezolizumab** is a monoclonal antibody that inhibits programmed death-ligand 1 (PD-L1), blocking its interaction with the PD-1 receptor to promote anti-tumor immune responses. The other agents—**oxaliplatin** (a platinum-based chemotherapeutic that induces DNA crosslinks and apoptosis), **leucovorin** (a folinic acid that enhances 5-fluorouracil efficacy), and **5-fluorouracil** (an antimetabolite inhibiting thymidylate synthase and DNA synthesis)—form the standard FOLFOX chemotherapy backbone. The combination is intended to synergize cytotoxic chemotherapy with immune checkpoint inhibition to improve disease-free survival in high-risk, surgically resected stage III colon cancer patients with dMMR[1][3][5].

Other names
atezolizumab plus FOLFOXatezolizumab + FOLFOXatezolizumab plus oxaliplatin/leucovorin/fluorouracil
02

Targets

TS (Thymidylate synthase)CD274 (Programmed cell death protein 1 ligand 1)DNA

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