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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, Jose
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.issued2022-06
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.description.versionSi
dc.identifier.citationMinchom A, Viteri S, Bazhenova L, Gadgeel SM, Ou SI, Trigo J, et al. 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. Lung Cancer. 2022 Jun;168:74-82.
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.provenanceRealizada la curación de contenido 08/08/2025.
dc.publisherElsevier
dc.pubmedtypeJournal Article
dc.pubmedtypeResearch Support, Non-U.S. Gov't
dc.relation.publisherversionhttps://linkinghub.elsevier.com/retrieve/pii/S0169-5002(22)00374-9
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.decsCarcinoma pulmonar de células no pequeñas
dc.subject.decsMutación
dc.subject.decsAnticuerpos monoclonales
dc.subject.decsInmunoterapia
dc.subject.decsInhibidores de proteincinasas
dc.subject.decsCompuestos de platino
dc.subject.decsSupervivencia libre de progresión
dc.subject.decsTasa de supervivencia
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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