Abstract
In the randomized, double-blind, multicenter study by Wang et al.,1 the addition of serplulimab (a PD-1 antibody) to anti-VEGF (HLX04; a bevacizumab biosimilar) together with chemotherapy (XELOX) was deemed to be tolerable and safe and may improve progression-free survival. However, even if adverse events were comparable, oncological endpoints including survival need to be confirmed in the next phase 3 study.
Keywords:
Translation to patients.
Copyright © 2024 Elsevier Inc. All rights reserved.
MeSH terms
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Antibodies, Monoclonal, Humanized / pharmacology
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Antibodies, Monoclonal, Humanized / therapeutic use
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Antineoplastic Combined Chemotherapy Protocols* / pharmacology
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Antineoplastic Combined Chemotherapy Protocols* / therapeutic use
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Bevacizumab / administration & dosage
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Bevacizumab / pharmacology
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Bevacizumab / therapeutic use
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Capecitabine* / administration & dosage
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Capecitabine* / therapeutic use
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Colorectal Neoplasms* / drug therapy
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Colorectal Neoplasms* / pathology
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Deoxycytidine / administration & dosage
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Deoxycytidine / analogs & derivatives
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Deoxycytidine / therapeutic use
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Humans
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Immune Checkpoint Inhibitors / pharmacology
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Immune Checkpoint Inhibitors / therapeutic use
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Oxaloacetates
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Programmed Cell Death 1 Receptor / antagonists & inhibitors
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Progression-Free Survival
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Vascular Endothelial Growth Factor A* / antagonists & inhibitors
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Vascular Endothelial Growth Factor A* / immunology
Substances
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Capecitabine
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Vascular Endothelial Growth Factor A
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Oxaloacetates
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Bevacizumab
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Programmed Cell Death 1 Receptor
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Immune Checkpoint Inhibitors
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Antibodies, Monoclonal, Humanized
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Deoxycytidine