2023
DOI: 10.1016/j.cllc.2022.11.004
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Amivantamab, an Epidermal Growth Factor Receptor (EGFR) and Mesenchymal-epithelial Transition Factor (MET) Bispecific Antibody, Designed to Enable Multiple Mechanisms of Action and Broad Clinical Applications

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Cited by 41 publications
(16 citation statements)
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“…Prior to 2022, no targeted therapy was available for lung cancer patients with EGFR exon 20 insertions. At the time of this report, amivantamab is approved by the United States Food and Drugs Administration (FDA), only for subsequent lines of therapy [ 8 ]. The approval was based on data from a multi-cohort study of 81 patients who developed disease progression after platinum-based chemotherapy.…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…Prior to 2022, no targeted therapy was available for lung cancer patients with EGFR exon 20 insertions. At the time of this report, amivantamab is approved by the United States Food and Drugs Administration (FDA), only for subsequent lines of therapy [ 8 ]. The approval was based on data from a multi-cohort study of 81 patients who developed disease progression after platinum-based chemotherapy.…”
Section: Discussionmentioning
confidence: 99%
“…In a study of 109 patients published in 2021, chemotherapy was found superior to conventional TKIs among patients with EGFR exon 20 insertions [ 7 ]. In this report, we described our experience treating a patient with EGFR exon 20 insertions with platinum-based chemotherapy, followed by amivantamab-a novel targeted therapy [ 8 ].…”
Section: Introductionmentioning
confidence: 99%
“…In two phase III trials, FLEX and BMS099, a combination of cetuximab and platinum doublet chemotherapy was employed to treat advanced NSCLC [ 22 , 23 ]. Additionally, amivantamab, a bispecific antibody targeting both EGFR and MET, was used to treat NSCLC specifically associated with EGFR exon 20 insertions [ 24 ]. In a preclinical study, the combination of amivantamab and lazertinib, which targets both the EGFR extracellular and catalytic domains, demonstrated synergistic tumor growth inhibition [ 25 ].…”
Section: Targeted Therapiesmentioning
confidence: 99%
“…This is a fully humanized antibody directed against mutated EGFR and mutated or amplified MET. It exerts its function both via the inhibition of the ligand binding and antibody-dependent cellular cytotoxicity ( 27 ). This drug is combined with lazertinib, a potent brain-penetrant third-generation EGFR TKI, and investigated in three clinical trials (CHRYSALIS, CHRYSALIS-2, MARIPOSA-2) for patients progressing during or after osimertinib.…”
Section: Combination Strategiesmentioning
confidence: 99%