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Use of archival versus newly collected tumor samples for assessing PD-L1 expression and overall survival: an updated analysis of KEYNOTE-010 trial.
Herbst, R S; Baas, P; Perez-Gracia, J L; Felip, E; Kim, D-W; Han, J-Y; Molina, J R; Kim, J-H; Dubos Arvis, C; Ahn, M-J; Majem, M; Fidler, M J; Surmont, V; de Castro, G; Garrido, M; Shentu, Y; Emancipator, K; Samkari, A; Jensen, E H; Lubiniecki, G M; Garon, E B.
Afiliação
  • Herbst RS; Department of Medical Oncology, Yale University School of Medicine, Yale Comprehensive Cancer Center, New Haven, USA. Electronic address: roy.herbst@yale.edu.
  • Baas P; Department of Thoracic Oncology, Netherlands Cancer Institute, Amsterdam, The Netherlands.
  • Perez-Gracia JL; Department of Oncology, Clinica Universidad de Navarra, Pamplona, Spain.
  • Felip E; Lung Cancer Unit, Department of Oncology, Vall d'Hebron University Hospital, Barcelona, Spain; Vall d'Hebron Institute of Oncology, Barcelona, Spain.
  • Kim DW; Department of Internal Medicine, Seoul National University Hospital, Seoul, Republic of Korea.
  • Han JY; Division of Translational & Clinical Research, National Cancer Center, Goyang, Republic of Korea.
  • Molina JR; Department of Oncology, Mayo Clinic, Rochester, USA.
  • Kim JH; Department of Medical Oncology, CHA Bundang Medical Center, CHA University, Gyeonggi-Do, Republic of Korea.
  • Dubos Arvis C; Department of Medicine, Centre François Baclesse, Caen, France.
  • Ahn MJ; Division of Hematology and Oncology, Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Republic of Korea.
  • Majem M; Department of Medical Oncology, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain.
  • Fidler MJ; Division of Hematology Oncology, Rush University Medical Center, Chicago, USA.
  • Surmont V; Department of Respiratory Medicine/Thoracic Oncology, Universitar Ziekenhuis Ghent, Ghent, Belgium.
  • de Castro G; Department of Medical Oncology, Instituto do Câncer do Estado de São Paulo, Sao Paulo, Brazil.
  • Garrido M; Department of Hemato-Oncology, Pontificia Universidad Católica de Chile, Santiago, Chile.
  • Shentu Y; Department of Clinical Research, Merck & Co. Inc., Kenilworth, USA.
  • Emancipator K; Department of Clinical Research, Merck & Co. Inc., Kenilworth, USA.
  • Samkari A; Department of Clinical Research, Merck & Co. Inc., Kenilworth, USA.
  • Jensen EH; Department of Clinical Research, Merck & Co. Inc., Kenilworth, USA.
  • Lubiniecki GM; Department of Clinical Research, Merck & Co. Inc., Kenilworth, USA.
  • Garon EB; Department of Medicine, Division of Hematology/Oncology, David Geffen School of Medicine at UCLA, Los Angeles, USA.
Ann Oncol ; 30(2): 281-289, 2019 02 01.
Article em En | MEDLINE | ID: mdl-30657853
BACKGROUND: In KEYNOTE-010, pembrolizumab versus docetaxel improved overall survival (OS) in patients with programmed death-1 protein (PD)-L1-positive advanced non-small-cell lung cancer (NSCLC). A prespecified exploratory analysis compared outcomes in patients based on PD-L1 expression in archival versus newly collected tumor samples using recently updated survival data. PATIENTS AND METHODS: PD-L1 was assessed centrally by immunohistochemistry (22C3 antibody) in archival or newly collected tumor samples. Patients received pembrolizumab 2 or 10 mg/kg Q3W or docetaxel 75 mg/m2 Q3W for 24 months or until progression/intolerable toxicity/other reason. Response was assessed by RECIST v1.1 every 9 weeks, survival every 2 months. Primary end points were OS and progression-free survival (PFS) in tumor proportion score (TPS) ≥50% and ≥1%; pembrolizumab doses were pooled in this analysis. RESULTS: At date cut-off of 24 March 2017, median follow-up was 31 months (range 23-41) representing 18 additional months of follow-up from the primary analysis. Pembrolizumab versus docetaxel continued to improve OS in patients with previously treated, PD-L1-expressing advanced NSCLC; hazard ratio (HR) was 0.66 [95% confidence interval (CI): 0.57, 0.77]. Of 1033 patients analyzed, 455(44%) were enrolled based on archival samples and 578 (56%) on newly collected tumor samples. Approximately 40% of archival samples and 45% of newly collected tumor samples were PD-L1 TPS ≥50%. For TPS ≥50%, the OS HRs were 0.64 (95% CI: 0.45, 0.91) and 0.40 (95% CI: 0.28, 0.56) for archival and newly collected samples, respectively. In patients with TPS ≥1%, OS HRs were 0.74 (95% CI: 0.59, 0.93) and 0.59 (95% CI: 0.48, 0.73) for archival and newly collected samples, respectively. In TPS ≥50%, PFS HRs were similar across archival [0.63 (95% CI: 0.45, 0.89)] and newly collected samples [0.53 (95% CI: 0.38, 0.72)]. In patients with TPS ≥1%, PFS HRs were similar across archival [0.82 (95% CI: 0.66, 1.02)] and newly collected samples [0.83 (95% CI: 0.68, 1.02)]. CONCLUSION: Pembrolizumab continued to improve OS over docetaxel in intention to treat population and in subsets of patients with newly collected and archival samples. TRIAL REGISTRATION: ClinicalTrials.gov: NCT01905657.
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Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Manejo de Espécimes / Carcinoma de Células Escamosas / Protocolos de Quimioterapia Combinada Antineoplásica / Carcinoma Pulmonar de Células não Pequenas / Antígeno B7-H1 / Neoplasias Pulmonares Tipo de estudo: Clinical_trials / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Ann Oncol Assunto da revista: NEOPLASIAS Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Manejo de Espécimes / Carcinoma de Células Escamosas / Protocolos de Quimioterapia Combinada Antineoplásica / Carcinoma Pulmonar de Células não Pequenas / Antígeno B7-H1 / Neoplasias Pulmonares Tipo de estudo: Clinical_trials / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Ann Oncol Assunto da revista: NEOPLASIAS Ano de publicação: 2019 Tipo de documento: Article