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Randomized Phase III Trial of Erlotinib versus Docetaxel in Patients with Advanced Squamous Cell Non-Small Cell Lung Cancer Failing First-Line Platinum-Based Doublet Chemotherapy Stratified by VeriStrat Good versus VeriStrat Poor. The European Thoracic Oncology Platform (ETOP) EMPHASIS-lung Trial.
Peters, Solange; Stahel, Rolf A; Dafni, Urania; Ponce Aix, Santiago; Massutí, Bartomeu; Gautschi, Oliver; Coate, Linda; López Martín, Ana; van Heemst, Robbert; Berghmans, Thierry; Meldgaard, Peter; Cobo Dols, Manuel; Garde Noguera, Javier; Curioni-Fontecedro, Alessandra; Rauch, Daniel; Mark, Michael T; Cuffe, Sinead; Biesma, Bonne; van Henten, Arjen M J; Juan Vidal, Óscar; Palmero Sanchez, Ramón; Villa Guzmán, José Carlos; Collado Martin, Ricardo; Peralta, Sergio; Insa, Amelia; Summers, Yvonne; Láng, István; Horgan, Anne; Ciardiello, Fortunato; de Hosson, Sander; Pieterman, Remge; Groen, Harry J M; van den Berg, Paul M; Zielinski, Christoph C; Chittazhathu Kurian Kuruvilla, Yojena; Gasca-Ruchti, Adriana; Kassapian, Marie; Novello, Silvia; Torri, Valter; Tsourti, Zoi; Gregorc, Vanesa; Smit, Egbert F.
Afiliação
  • Peters S; University Hospital of Lausanne (CHUV), Lausanne, Switzerland. Electronic address: Solange.Peters@chuv.ch.
  • Stahel RA; University Hospital Zürich, Clinic of Oncology, Zürich, Switzerland.
  • Dafni U; Frontier Science Foundation-Hellas and National and Kapodistrian University of Athens, Athens, Greece.
  • Ponce Aix S; University Hospital 12 de Octubre, Madrid, Spain.
  • Massutí B; Alicante University Hospital, Alicante, Spain.
  • Gautschi O; Swiss Group for Clinical Cancer Research and Cantonal Hospital Lucerne, Switzerland.
  • Coate L; Cancer Trials Ireland and Mid-Western Regional Hospital, Limerick, Ireland.
  • López Martín A; University Hospital Severo Ochoa, Madrid, Spain.
  • van Heemst R; Deventer Hospital, Deventer, The Netherlands.
  • Berghmans T; Institute Jules Bordet, Brussels, Belgium.
  • Meldgaard P; Aarhus University Hospital, Aarhus, Denmark.
  • Cobo Dols M; University Hospital Virgen de la Victoria, Malaga, Spain.
  • Garde Noguera J; Hospital Arnau Vilanova, Valencia, Spain.
  • Curioni-Fontecedro A; University Hospital Zürich, Clinic of Oncology, Zürich, Switzerland.
  • Rauch D; Cantonal Hospital, Thun, Switzerland.
  • Mark MT; Cantonal Hospital, Chur, Switzerland.
  • Cuffe S; Cancer Trials Ireland and St. James's Hospital, Dublin, Ireland.
  • Biesma B; Jeroen Bosch Hospital, 's-Hertogenbosch, The Netherlands.
  • van Henten AMJ; Maxima Medical Centre, Eindhoven, The Netherlands.
  • Juan Vidal Ó; Hospital La Fe, Valencia, Spain.
  • Palmero Sanchez R; Hospital Duran i Reynalds, Barcelona, Spain.
  • Villa Guzmán JC; General University Hospital, Ciudad Real, Spain.
  • Collado Martin R; Hospital San Pedro de Alcantara, Spain.
  • Peralta S; Hospital Sant Joan de Reus, Spain.
  • Insa A; University Hospital, Valencia, Spain.
  • Summers Y; Christie Hospital Manchester, United Kingdom.
  • Láng I; National Institute of Oncology, Budapest, Hungary.
  • Horgan A; Cancer Trials Ireland and University Hospital Waterford, Ireland.
  • Ciardiello F; Second University of Naples, Naples, Italy.
  • de Hosson S; Wilhelmina Hospital, Assen, The Netherlands.
  • Pieterman R; Ommelander Hospital Group, Winschoten, The Netherlands.
  • Groen HJM; University Medical Center Groningen, The Netherlands.
  • van den Berg PM; Maasstad Hospital, Rotterdam, The Netherlands.
  • Zielinski CC; Central European Cooperative Oncology Group and Comprehensive Cancer Center of the Medical University, Vienna, Austria.
  • Chittazhathu Kurian Kuruvilla Y; European Thoracic Oncology Platform Coordinating Office, Bern, Switzerland.
  • Gasca-Ruchti A; European Thoracic Oncology Platform Coordinating Office, Bern, Switzerland.
  • Kassapian M; Frontier Science Foundation-Hellas, Athens, Greece.
  • Novello S; University of Turin, Department of Clinical and Biological Sciences, Turin, Italy.
  • Torri V; Mario Negri Institute for Pharmacological Research, Milan, Italy.
  • Tsourti Z; Frontier Science Foundation-Hellas, Athens, Greece.
  • Gregorc V; IRCCS Scientific Institute Ospedale San Raffaele, Milan, Italy.
  • Smit EF; Cancer Center Amsterdam, VU University Medical Center, Amsterdam, The Netherlands.
J Thorac Oncol ; 12(4): 752-762, 2017 04.
Article em En | MEDLINE | ID: mdl-28017787
ABSTRACT

INTRODUCTION:

Docetaxel and erlotinib are registered second-line treatments for wild-type EGFR NSCLC. Previous studies suggested a predictive value of the VeriStrat test in second-line therapy of NSCLC, classifying patients as either VeriStrat good or VeriStrat poor. EMPHASIS-lung aimed at exploring this predictive effect in patients with squamous cell NSCLC. The trial closed prematurely because of low accrual and results from other trials. Our analysis includes an exploratory combined analysis with results from the PROSE trial.

METHODS:

EMPHASIS-lung was a randomized phase III multicenter trial exploring the differential effect of second-line erlotinib versus docetaxel on progression-free survival (PFS) in VeriStrat good versus VeriStrat poor patients with squamous cell NSCLC.

RESULTS:

A total of 80 patients were randomized, with 72.5% categorized as VeriStrat good. Patient characteristics were balanced between VeriStrat status and treatment groups. The median PFS times with docetaxel and erlotinib treatment in the VeriStrat good cohort were 4.1 and 1.6 months, respectively, versus 1.9 and 2.1 months, respectively, in the VeriStrat poor cohort. The median overall survival (OS) times with docetaxel and erlotinib treatment in the VeriStrat good cohort were 7.8 and 8.4 months, respectively, and 4.4 and 5.2 months, respectively, in the VeriStrat poor cohort. An additional exploratory analysis was performed; in it, 47 patients from the squamous cell subgroup of PROSE were included in a combined analysis, contributing with 45 PFS and 41 OS events.

CONCLUSIONS:

The final analysis of EMPHASIS-lung did not show a differential effect on PFS for erlotinib versus docetaxel stratified by VeriStrat status. Similarly, in the combined analysis, no significant treatment by VeriStrat status interaction was observed (interaction p = 0.24 for PFS and 0.45 for OS, stratified by study).
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Carcinoma de Células Escamosas / Protocolos de Quimioterapia Combinada Antineoplásica / Carcinoma Pulmonar de Células não Pequenas / Neoplasias Pulmonares Tipo de estudo: Clinical_trials / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Female / Humans / Male Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Carcinoma de Células Escamosas / Protocolos de Quimioterapia Combinada Antineoplásica / Carcinoma Pulmonar de Células não Pequenas / Neoplasias Pulmonares Tipo de estudo: Clinical_trials / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Female / Humans / Male Idioma: En Ano de publicação: 2017 Tipo de documento: Article