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.author | Minchom, Anna | |
dc.contributor.author | Viteri, Santiago | |
dc.contributor.author | Bazhenova, Lyudmila | |
dc.contributor.author | Gadgeel, Shirish M | |
dc.contributor.author | Ou, Sai-Hong Ignatius | |
dc.contributor.author | Trigo, José | |
dc.contributor.author | Bauml, Joshua M | |
dc.contributor.author | Backenroth, Daniel | |
dc.contributor.author | Bhattacharya, Archan | |
dc.contributor.author | Li, Tracy | |
dc.contributor.author | Mahadevia, Parthiv | |
dc.contributor.author | Girard, Nicolas | |
dc.date.accessioned | 2023-05-03T15:07:30Z | |
dc.date.available | 2023-05-03T15:07:30Z | |
dc.date.issued | 2022-03-08 | |
dc.description.abstract | In 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.doi | 10.1016/j.lungcan.2022.03.005 | |
dc.identifier.essn | 1872-8332 | |
dc.identifier.pmid | 35597172 | |
dc.identifier.unpaywallURL | http://www.lungcancerjournal.info/article/S0169500222003749/pdf | |
dc.identifier.uri | http://hdl.handle.net/10668/22353 | |
dc.journal.title | Lung cancer (Amsterdam, Netherlands) | |
dc.journal.titleabbreviation | Lung Cancer | |
dc.language.iso | en | |
dc.organization | Hospital Universitario Virgen de la Victoria | |
dc.organization | Instituto de Investigación Biomédica de Málaga-IBIMA | |
dc.page.number | 74-82 | |
dc.pubmedtype | Journal Article | |
dc.pubmedtype | Research Support, Non-U.S. Gov't | |
dc.rights | Attribution-NonCommercial-NoDerivatives 4.0 International | |
dc.rights.accessRights | open access | |
dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/4.0/ | |
dc.subject | Amivantamab | |
dc.subject | Epidermal growth factor receptor | |
dc.subject | Exon 20 insertion | |
dc.subject | Non-small cell lung cancer | |
dc.subject | Real world | |
dc.subject.mesh | Antibodies, Bispecific | |
dc.subject.mesh | Antineoplastic Combined Chemotherapy Protocols | |
dc.subject.mesh | Carcinoma, Non-Small-Cell Lung | |
dc.subject.mesh | ErbB Receptors | |
dc.subject.mesh | Exons | |
dc.subject.mesh | Humans | |
dc.subject.mesh | Lung Neoplasms | |
dc.subject.mesh | Mutagenesis, Insertional | |
dc.subject.mesh | Mutation | |
dc.subject.mesh | Platinum | |
dc.subject.mesh | Protein Kinase Inhibitors | |
dc.title | 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.type | research article | |
dc.type.hasVersion | VoR | |
dc.volume.number | 168 | |
dspace.entity.type | Publication |