Publication:
Amivantamab compared with real-world therapies in patients with advanced non-small cell lung cancer harboring EGFR exon 20 insertion mutations who progressed after platinum-based chemotherapy.

dc.contributor.authorMinchom, Anna
dc.contributor.authorViteri, Santiago
dc.contributor.authorBazhenova, Lyudmila
dc.contributor.authorGadgeel, Shirish M
dc.contributor.authorOu, Sai-Hong Ignatius
dc.contributor.authorTrigo, José
dc.contributor.authorBauml, Joshua M
dc.contributor.authorBackenroth, Daniel
dc.contributor.authorBhattacharya, Archan
dc.contributor.authorLi, Tracy
dc.contributor.authorMahadevia, Parthiv
dc.contributor.authorGirard, Nicolas
dc.date.accessioned2023-05-03T15:07:30Z
dc.date.available2023-05-03T15:07:30Z
dc.date.issued2022-03-08
dc.description.abstractIn the single-arm CHRYSALIS study, amivantamab showed durable responses and manageable safety in patients with advanced non-small cell lung cancer (NSCLC) harboring epidermal growth factor receptor (EGFR) exon 20 insertion mutations (ex20ins) who progressed on prior platinum-based chemotherapy. External controls can provide context for interpreting amivantamab efficacy. External controls were selected from three US-based databases (ConcertAI, COTA, and Flatiron). Key inclusion criteria were diagnosis of EGFR ex20ins advanced NSCLC, prior platinum-based chemotherapy, and performance status score ≤ 1. Duplicate external controls were identified using a tokenization procedure and removed, and adjustment for differences in baseline characteristics between amivantamab-treated and external control cohorts was achieved using propensity score weighting. Amivantamab-treated and pooled external control cohorts included 81 and 125 patients, respectively. Baseline characteristics were generally similar across cohorts, except more amivantamab-treated patients were Asian (56% vs 13%). Most common therapies received by external controls were non-platinum-based chemotherapy (25.1%), immuno-oncology therapies (24.2%), EGFR tyrosine kinase inhibitors (16.3%), and platinum-based chemotherapy (16.3%). Overall response rate was 40% among amivantamab-treated patients and 16% among external controls. Amivantamab-treated patients had longer progression-free survival (median 8.3 vs 2.9 months; hazard ratio [HR; 95% CI]: 0.47 [0.34-0.65]), time to next therapy (median 14.8 vs 4.8 months; HR [95% CI]: 0.40 [0.28-0.57]), and overall survival (median 22.8 vs 12.8 months; HR [95% CI]: 0.49 [0.31-0.77]) than external controls. Results were consistent in sensitivity analyses comparing each external control dataset against the amivantamab-treated group separately. Among post-platinum patients with EGFR ex20ins advanced NSCLC, those treated with amivantamab had improved outcomes, including 10-month longer overall survival, versus external controls.
dc.identifier.doi10.1016/j.lungcan.2022.03.005
dc.identifier.essn1872-8332
dc.identifier.pmid35597172
dc.identifier.unpaywallURLhttp://www.lungcancerjournal.info/article/S0169500222003749/pdf
dc.identifier.urihttp://hdl.handle.net/10668/22353
dc.journal.titleLung cancer (Amsterdam, Netherlands)
dc.journal.titleabbreviationLung Cancer
dc.language.isoen
dc.organizationHospital Universitario Virgen de la Victoria
dc.organizationInstituto de Investigación Biomédica de Málaga-IBIMA
dc.page.number74-82
dc.pubmedtypeJournal Article
dc.pubmedtypeResearch Support, Non-U.S. Gov't
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subjectAmivantamab
dc.subjectEpidermal growth factor receptor
dc.subjectExon 20 insertion
dc.subjectNon-small cell lung cancer
dc.subjectReal world
dc.subject.meshAntibodies, Bispecific
dc.subject.meshAntineoplastic Combined Chemotherapy Protocols
dc.subject.meshCarcinoma, Non-Small-Cell Lung
dc.subject.meshErbB Receptors
dc.subject.meshExons
dc.subject.meshHumans
dc.subject.meshLung Neoplasms
dc.subject.meshMutagenesis, Insertional
dc.subject.meshMutation
dc.subject.meshPlatinum
dc.subject.meshProtein Kinase Inhibitors
dc.titleAmivantamab compared with real-world therapies in patients with advanced non-small cell lung cancer harboring EGFR exon 20 insertion mutations who progressed after platinum-based chemotherapy.
dc.typeresearch article
dc.type.hasVersionVoR
dc.volume.number168
dspace.entity.typePublication

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