Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/27713
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dc.contributor.authorReck, M-
dc.contributor.authorCiuleanu, T-E-
dc.contributor.authorCobo, M-
dc.contributor.authorSchenker, M-
dc.contributor.authorZurawski, B-
dc.contributor.authorMenezes, J-
dc.contributor.authorRichardet, E-
dc.contributor.authorBennouna, J-
dc.contributor.authorFelip, E-
dc.contributor.authorJuan-Vidal, O-
dc.contributor.authorAlexandru, A-
dc.contributor.authorSakai, H-
dc.contributor.authorLingua, A-
dc.contributor.authorReyes, F-
dc.contributor.authorSouquet, P-J-
dc.contributor.authorDe Marchi, P-
dc.contributor.authorMartin, C-
dc.contributor.authorPérol, M-
dc.contributor.authorScherpereel, A-
dc.contributor.authorLu, S-
dc.contributor.authorPaz-Ares, L-
dc.contributor.authorCarbone, D P-
dc.contributor.authorMemaj, A-
dc.contributor.authorMarimuthu, S-
dc.contributor.authorZhang, X-
dc.contributor.authorTran, P-
dc.contributor.authorJohn, Thomas-
dc.date2021-10-01-
dc.date.accessioned2021-10-11T04:12:47Z-
dc.date.available2021-10-11T04:12:47Z-
dc.date.issued2021-10-01-
dc.identifier.citationESMO Open 2021; 6(5): 100273en
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/27713-
dc.description.abstractTo further characterize survival benefit with first-line nivolumab plus ipilimumab with two cycles of chemotherapy versus chemotherapy alone, we report updated data from the phase III CheckMate 9LA trial with a 2-year minimum follow-up. Adult patients were treatment naïve, with stage IV/recurrent non-small-cell lung cancer, no known sensitizing EGFR/ALK alterations, and an Eastern Cooperative Oncology Group performance status ≤1. Patients were randomized 1 : 1 to nivolumab 360 mg every 3 weeks plus ipilimumab 1 mg/kg every 6 weeks with two cycles of chemotherapy, or four cycles of chemotherapy. Updated efficacy and safety outcomes are reported, along with progression-free survival (PFS) after next line of treatment (PFS2), treatment-related adverse events (TRAEs) by treatment cycle, and efficacy outcomes in patients who discontinued all treatment components in the experimental arm due to TRAEs. With a median follow-up of 30.7 months, nivolumab plus ipilimumab with chemotherapy continued to prolong overall survival (OS) versus chemotherapy. Median OS was 15.8 versus 11.0 months [hazard ratio 0.72 (95% confidence interval 0.61-0.86)]; 2-year OS rate was 38% versus 26%. Two-year PFS rate was 20% versus 8%. ORR was 38% versus 25%, respectively; 34% versus 12% of all responses were ongoing at 2 years. Median PFS2 was 13.9 versus 8.7 months. Improved efficacy outcomes in the experimental versus control arm were observed across most subgroups, including by programmed death-ligand 1 and histology. No new safety signals were observed; onset of grade 3/4 TRAEs was mostly observed during the first two treatment cycles in the experimental arm. In patients who discontinued all components of nivolumab plus ipilimumab with chemotherapy treatment due to TRAEs (n = 61) median OS was 27.5 months; 56% of responders had an ongoing response ≥1 year after discontinuation. With a 2-year minimum follow-up, nivolumab plus ipilimumab with two cycles of chemotherapy provided durable efficacy benefits over chemotherapy with a manageable safety profile and remains an efficacious first-line treatment of advanced non-small-cell lung cancer.en
dc.language.isoeng
dc.subjectNSCLCen
dc.subjectdual immunotherapyen
dc.subjectfirst-lineen
dc.subjectipilimumaben
dc.subjectnivolumaben
dc.titleFirst-line nivolumab plus ipilimumab with two cycles of chemotherapy versus chemotherapy alone (four cycles) in advanced non-small-cell lung cancer: CheckMate 9LA 2-year update.en
dc.typeJournal Articleen
dc.identifier.journaltitleESMO Openen
dc.identifier.affiliationDepartment of Thoracic Oncology, Airway Research Center North, German Center for Lung Research, LungClinic, Grosshansdorf, Germany.en
dc.identifier.affiliationBristol Myers Squibb, Princeton, USAen
dc.identifier.affiliationMedical Oncologyen
dc.identifier.affiliationDepartment of Medical Oncology, The Ohio State University Comprehensive Cancer Center, Columbus, USAen
dc.identifier.affiliationDepartment of Oncology, Institutul Oncologic Prof Dr Ion Chiricuta and UMF Iuliu Hatieganu, Cluj-Napoca, Romaniaen
dc.identifier.affiliationDepartment of Medical Oncology, Unidad de Gestión Clínica Intercentros de Oncología Médica, Hospitales Universitarios Regional y Virgen de la Victoria, IBIMA, Málaga, Spainen
dc.identifier.affiliationDepartment of Oncology, SF Nectarie Oncology Center, Craiova, Romaniaen
dc.identifier.affiliationDepartment of Clinical Oncology, Ambulatorium Chemioterapii, Bydgoszcz, Polanden
dc.identifier.affiliationDepartment of Oncology, Hospital Nossa Senhora da Conceição, Porto Alegre, Brazilen
dc.identifier.affiliationDepartment of Clinical Oncology, Instituto Oncológico de Córdoba, Córdoba, Argentinaen
dc.identifier.affiliationDepartment of Thoracic Oncology, University Hospital of Nantes and INSERM, CRCINA, Nantes, Franceen
dc.identifier.affiliationDepartment of Medical Oncology, Vall d'Hebron University Hospital, Vall d'Hebron Institute of Oncology, Barcelonaen
dc.identifier.affiliationDepartment of Medical Oncology, Hospital Universitario La Fe, Valencia, Spainen
dc.identifier.affiliationDepartment of Oncology, Institute of Oncology Prof Dr Alexandru Trestioreanu Bucha, Bucharest, Romaniaen
dc.identifier.affiliationDepartment of Thoracic Oncology, Saitama Cancer Center, Saitama, Japanen
dc.identifier.affiliationDepartment of Medical Oncology, Instituto Medico Rio Cuarto, SA, Córdoba, Argentinaen
dc.identifier.affiliationDepartment of Medical Oncology, Fundación Arturo López Pérez, Santiago, Metropolitana, Chileen
dc.identifier.affiliationDepartment of Pneumology, Hôpital Lyon Sud, Lyon, Pierre Bénite, Franceen
dc.identifier.affiliationDepartment of Oncology, Barretos Cancer Hospital, Barretos, Brazilen
dc.identifier.affiliationDepartment of Thoracic Oncology, Instituto Alexander Fleming, Buenos Aires, Argentinaen
dc.identifier.affiliationDepartment of Thoracic Oncology, Léon Bérard Cancer Center, Lyon, Franceen
dc.identifier.affiliationDepartment of Pulmonary and Thoracic Oncology, University of Lille, CHU Lille, INSERM U1189, OncoThAI, Lille, Franceen
dc.identifier.affiliationDepartment of Medical Oncology, Shanghai Lung Cancer Center, Shanghai Chest Hospital, Shanghai JiaoTong University, Shanghai, Chinaen
dc.identifier.affiliationDepartment of Medical Oncology, Hospital Universitario 12 de Octubre, CNIO-H12o Lung Cancer Clinical Research Unit, Universidad Complutense & CiberOnc, Madrid, Spainen
dc.identifier.doi10.1016/j.esmoop.2021.100273en
dc.type.contentTexten
dc.identifier.pubmedid34607285
local.name.researcherJohn, Thomas
item.cerifentitytypePublications-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextNo Fulltext-
item.openairetypeJournal Article-
item.grantfulltextnone-
item.languageiso639-1en-
crisitem.author.deptOlivia Newton-John Cancer Research Institute-
crisitem.author.deptMedical Oncology-
crisitem.author.deptOlivia Newton-John Cancer Wellness and Research Centre-
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