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nab-Paclitaxel Plus Durvalumab in Patients With Previously Treated Advanced Stage Non-small Cell Lung Cancer (ABOUND.2L+).
Morgensztern, Daniel; Dols, Manuel Cobo; Ponce Aix, Santiago; Postmus, Pieter E; Bennouna, Jaafar; Fischer, Jürgen R; Juan-Vidal, Oscar; Stewart, David J; Ardizzoni, Andrea; Bhore, Rafia; Wolfsteiner, Marianne; Reck, Martin; Talbot, Denis; Govindan, Ramaswamy; Ong, Teng Jin.
Afiliação
  • Morgensztern D; Washington University School of Medicine, St Louis, MO, United States.
  • Dols MC; Hospital Universitario Málaga Regional, Instituto de Investigación Biomédica de Málaga (IBIMA), Málaga, Spain.
  • Ponce Aix S; Unidad de Investigación Clínica de Cáncer Pulmón H12O-CNIO, Madrid, Spain.
  • Postmus PE; Clatterbridge Cancer Center, Liverpool, United Kingdom.
  • Bennouna J; Centre René Gauducheau Centre de Lutte Contre Le Cancer Nantes Atlantique, Nantes, France.
  • Fischer JR; Lungenklinik Löwenstein gGmbH, Löwenstein, Germany.
  • Juan-Vidal O; Universitari i Politécnic La Fe, Valencia, Spain.
  • Stewart DJ; Ottawa Hospital, Ottawa, ON, Canada.
  • Ardizzoni A; Azienda Ospedaliero Universitaria Di Bologna-Policlinico S. Orsola-Malpighi, Bologna, Italy.
  • Bhore R; Bristol Myers Squibb, Princeton, NJ, United States.
  • Wolfsteiner M; Pharmaceutical Research Associates Inc. (PRA) Health Sciences, Lenexa, KS, United States.
  • Reck M; LungenClinic, Grosshansdorf, Germany.
  • Talbot D; Churchill Hospital, Oxford, United Kingdom.
  • Govindan R; Washington University School of Medicine, St Louis, MO, United States.
  • Ong TJ; Bristol Myers Squibb, Princeton, NJ, United States.
Front Oncol ; 10: 569715, 2020.
Article em En | MEDLINE | ID: mdl-33643895
Background: The standard therapy for advanced stage non-small cell lung cancer (NSCLC) with no actionable gene alterations is a platinum-based chemotherapy doublet and immune checkpoint blocker (ICB), either concurrently or sequentially, followed by docetaxel at the time of tumor progression. However, more effective treatments are needed. We evaluated the nab-paclitaxel and durvalumab combination in patients with previously treated advanced stage NSCLC. Methods: Patients with advanced stage NSCLC previously treated with one line of platinum-based doublet with or without an ICB and no activating EGFR mutations or ALK translocations received nab-paclitaxel 100 mg/m2 (days 1 and 8) plus durvalumab 1,125 mg (day 15) every 21 days. The primary endpoint was progression-free survival (PFS). Key secondary endpoints included overall survival (OS) and safety. Results: Between February 2016 and December 2016, 79 patients were enrolled. The median age was 63 years. Most patients were males (68.4%), had non-squamous histology (69.6%), and had no prior ICB treatment (88.6%). The median PFS was 4.5 months; median OS was 10.1 months. A post hoc analysis of survival by prior ICB treatment revealed a median PFS and OS of 4.4 and 9.9 months, respectively, in ICB-naive patients and 6.9 months and not estimable, respectively, in patients previously treated with ICB. The most common treatment-emergent adverse events were asthenia (46.2%) and diarrhea (34.6%); four treatment-related deaths (5.1%) occurred. Conclusions: The nab-paclitaxel and durvalumab combination is feasible and demonstrated antitumor activity without new safety signals. Additional studies using taxanes and ICB in patients with previously treated NSCLC are warranted. Clinical Trial Registration: ClinicalTrials.gov registration (NCT02250326). EudraCT number: 2014-001105-41.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Front Oncol Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Front Oncol Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Estados Unidos