Publication:
Overall Survival and Biomarker Analysis of Neoadjuvant Nivolumab Plus Chemotherapy in Operable Stage IIIA Non-Small-Cell Lung Cancer (NADIM phase II trial).

dc.contributor.authorProvencio, Mariano
dc.contributor.authorSerna-Blasco, Roberto
dc.contributor.authorNadal, Ernest
dc.contributor.authorInsa, Amelia
dc.contributor.authorGarcía-Campelo, M Rosario
dc.contributor.authorCasal Rubio, Joaquín
dc.contributor.authorDómine, Manuel
dc.contributor.authorMajem, Margarita
dc.contributor.authorRodríguez-Abreu, Delvys
dc.contributor.authorMartínez-Martí, Alex
dc.contributor.authorDe Castro Carpeño, Javier
dc.contributor.authorCobo, Manuel
dc.contributor.authorLópez Vivanco, Guillermo
dc.contributor.authorDel Barco, Edel
dc.contributor.authorBernabé Caro, Reyes
dc.contributor.authorViñolas, Nuria
dc.contributor.authorBarneto Aranda, Isidoro
dc.contributor.authorViteri, Santiago
dc.contributor.authorPereira, Eva
dc.contributor.authorRoyuela, Ana
dc.contributor.authorCalvo, Virginia
dc.contributor.authorMartín-López, Javier
dc.contributor.authorGarcía-García, Francisco
dc.contributor.authorCasarrubios, Marta
dc.contributor.authorFranco, Fernando
dc.contributor.authorSánchez-Herrero, Estela
dc.contributor.authorMassuti, Bartomeu
dc.contributor.authorCruz-Bermúdez, Alberto
dc.contributor.authorRomero, Atocha
dc.date.accessioned2023-05-03T13:35:40Z
dc.date.available2023-05-03T13:35:40Z
dc.date.issued2022-05-16
dc.description.abstractNeoadjuvant chemotherapy plus nivolumab has been shown to be effective in resectable non-small-cell lung cancer (NSCLC) in the NADIM trial (ClinicalTrials.gov identifier: NCT03081689). The 3-year overall survival (OS) and circulating tumor DNA (ctDNA) analysis have not been reported. This was an open-label, multicenter, single-arm, phase II trial in which patients with stage IIIA NSCLC, who were deemed to be surgically resectable, were treated with neoadjuvant paclitaxel (200 mg/m2 once a day) and carboplatin (area under curve 6) plus nivolumab (360 mg) once on day 1 of each 21-day cycle, for three cycles, followed by adjuvant nivolumab monotherapy for 1 year (240 mg once every 2 weeks for 4 months, followed by 480 mg once every 4 weeks for 8 months). The 3-year OS and ctDNA analysis were secondary objectives of the trial. OS at 36 months was 81.9% (95% CI, 66.8 to 90.6) in the intention-to-treat population, rising to 91.0% (95% CI, 74.2 to 97.0) in the per-protocol population. Neither tumor mutation burden nor programmed cell death ligand-1 staining was predictive of survival. Conversely, low pretreatment levels of ctDNA were significantly associated with improved progression-free survival and OS (hazard ratio [HR], 0.20; 95% CI, 0.06 to 0.63, and HR, 0.07; 95% CI, 0.01 to 0.39, respectively). Clinical responses according to RECIST v1.1 criteria did not predict survival outcomes. However, undetectable ctDNA levels after neoadjuvant treatment were significantly associated with progression-free survival and OS (HR, 0.26; 95% CI, 0.07 to 0.93, and HR, 0.04; 95% CI, 0.00 to 0.55, respectively). The C-index to predict OS for ctDNA levels after neoadjuvant treatment (0.82) was superior to that of RECIST criteria (0.72). The efficacy of neoadjuvant chemotherapy plus nivolumab in resectable NSCLC is supported by 3-year OS. ctDNA levels were significantly associated with OS and outperformed radiologic assessments in the prediction of survival.
dc.identifier.doi10.1200/JCO.21.02660
dc.identifier.essn1527-7755
dc.identifier.pmcPMC9426809
dc.identifier.pmid35576508
dc.identifier.pubmedURLhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9426809/pdf
dc.identifier.unpaywallURLhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9426809
dc.identifier.urihttp://hdl.handle.net/10668/20389
dc.issue.number25
dc.journal.titleJournal of clinical oncology : official journal of the American Society of Clinical Oncology
dc.journal.titleabbreviationJ Clin Oncol
dc.language.isoen
dc.organizationHospital Universitario Reina Sofía
dc.organizationHospital Universitario Virgen del Rocío
dc.page.number2924-2933
dc.pubmedtypeClinical Trial, Phase II
dc.pubmedtypeJournal Article
dc.pubmedtypeMulticenter Study
dc.pubmedtypeResearch Support, Non-U.S. Gov't
dc.rights.accessRightsopen access
dc.subject.meshAntineoplastic Combined Chemotherapy Protocols
dc.subject.meshBiomarkers
dc.subject.meshCarcinoma, Non-Small-Cell Lung
dc.subject.meshHumans
dc.subject.meshLung Neoplasms
dc.subject.meshNeoadjuvant Therapy
dc.subject.meshNivolumab
dc.titleOverall Survival and Biomarker Analysis of Neoadjuvant Nivolumab Plus Chemotherapy in Operable Stage IIIA Non-Small-Cell Lung Cancer (NADIM phase II trial).
dc.typeresearch article
dc.type.hasVersionVoR
dc.volume.number40
dspace.entity.typePublication

Files

Original bundle

Now showing 1 - 1 of 1
Loading...
Thumbnail Image
Name:
PMC9426809.pdf
Size:
405.81 KB
Format:
Adobe Portable Document Format