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Atezolizumab in patients with advanced non-small cell lung cancer and history of asymptomatic, treated brain metastases: Exploratory analyses of the phase III OAK study.
Gadgeel, Shirish M; Lukas, Rimas V; Goldschmidt, Jerome; Conkling, Paul; Park, Keunchil; Cortinovis, Diego; de Marinis, Filippo; Rittmeyer, Achim; Patel, Jyoti D; von Pawel, Joachim; O'Hear, Carol; Lai, Catherine; Hu, Sylvia; Ballinger, Marcus; Sandler, Alan; Gandhi, Mayank; Fehrenbacher, Lou.
Afiliação
  • Gadgeel SM; University of Michigan, 1500 E. Medical Center Drive, 7217CC, Ann Arbor, MI 48109, USA. Electronic address: sgadgeel@med.umich.edu.
  • Lukas RV; Department of Neurology, Northwestern University, 710 N. Lake Shore Drive, Abbott Hall 1114, Chicago, IL 60611, USA. Electronic address: rimas.Lukas@nm.org.
  • Goldschmidt J; Blue Ridge Cancer Care, 2600 Research Center Drive, Suite A, Blacksburg, VA 24060, USA. Electronic address: jerome.goldschmidt@usoncology.com.
  • Conkling P; Virginia Oncology Associates, 5900 Lake Wright Drive, Norfolk, VA 23502, USA. Electronic address: paul.conkling@usoncology.com.
  • Park K; Samsung Medical Center, Sungkyunkwan University School of Medicine, 81 Irwon-ro, Gangnam-gu, Seoul, 135-710, Republic of Korea. Electronic address: kpark@skku.edu.
  • Cortinovis D; Medical Oncology Unit, AOU San Gerardo, Via Pergolesi 33 Monza, Lombardia 20141, Italy. Electronic address: d.cortinovis@asst-monza.it.
  • de Marinis F; European Institute of Oncology, IEO, IRCCS, Via Ripamonti 435, 20141, Milan, Italy. Electronic address: filippo.demarinis@ieo.it.
  • Rittmeyer A; Lungenfachklinik Immenhausen, Pneumologische Lehrklinik Universität Göttingen Robert-Koch-Str. 3, 34376 Immenhausen, Germany. Electronic address: a.rittmeyer@lungenfachklinik-immenhausen.de.
  • Patel JD; University of Chicago, 5841 S. Maryland Avenue, MC 2115, Chicago, IL 60637-1470, USA. Electronic address: jpatel25@medicine.bsd.uchicago.edu.
  • von Pawel J; Asklepios Fachkliniken München-Gauting, Gauting, Germany. Electronic address: j.pawel@asklepios.com.
  • O'Hear C; Genentech, Inc., 1 DNA Way, South San Francisco, CA 94080, USA. Electronic address: ohearc@gene.com.
  • Lai C; Genentech, Inc., 1 DNA Way, South San Francisco, CA 94080, USA. Electronic address: lai.catherine@gene.com.
  • Hu S; Genentech, Inc., 1 DNA Way, South San Francisco, CA 94080, USA. Electronic address: hu.sylvia@gene.com.
  • Ballinger M; Genentech, Inc., 1 DNA Way, South San Francisco, CA 94080, USA. Electronic address: ballinger.marcus@gene.com.
  • Sandler A; Genentech, Inc., 1 DNA Way, South San Francisco, CA 94080, USA. Electronic address: sandlera@gene.com.
  • Gandhi M; Genentech, Inc., 1 DNA Way, South San Francisco, CA 94080, USA. Electronic address: gandhi.mayank@gene.com.
  • Fehrenbacher L; Kaiser Permanente Medical Center, 975 Sereno Drive, Vallejo, CA 94589, USA. Electronic address: louis.fehrenbacher@gmail.com.
Lung Cancer ; 128: 105-112, 2019 02.
Article em En | MEDLINE | ID: mdl-30642441
OBJECTIVES: To assess the safety and efficacy of atezolizumab and docetaxel in patients with and without a history of asymptomatic, treated brain metastases in the phase III OAK trial. MATERIALS AND METHODS: Patients received 1200 mg atezolizumab or 75 mg/m2 docetaxel every 3 weeks until unacceptable toxicity, disease progression, or loss of clinical atezolizumab benefit. Patients with asymptomatic, treated supratentorial metastases were eligible. Patients had brain scans before enrollment; follow-up brain scans and treatment were required when clinically indicated. RESULTS: Approximately 14% of patients in each arm had a history of asymptomatic, treated brain metastases (61/425 in the atezolizumab arm and 62/425 in the docetaxel arm). Fewer treatment-related adverse events (AEs), serious AEs, and treatment-related neurologic AEs were reported with atezolizumab than with docetaxel, regardless of history of asymptomatic, treated brain metastases. In patients with a history of asymptomatic, treated brain metastases, median overall survival (OS) was longer with atezolizumab than with docetaxel (16.0 vs 11.9 months; hazard ratio = 0.74; 95% CI: 0.49-1.13). Median OS was also longer with atezolizumab in patients without a history of asymptomatic, treated brain metastases (13.2 vs 9.3 months; hazard ratio = 0.74; 95% CI: 0.63-0.88). Landmark analyses showed that patients with a history of asymptomatic, treated brain metastases had a lower probability of developing new symptomatic brain lesions with atezolizumab vs docetaxel at 6-24 months. Patients without a history had a lower probability with atezolizumab at 18-24+ months. CONCLUSION: Atezolizumab had an acceptable neurologic safety profile, showed a trend toward an OS benefit, and led to a prolonged time to radiographic identification of new symptomatic brain lesions compared with docetaxel in patients who had a history of asymptomatic, treated brain metastases. Clinicaltrials.gov registration number: NCT02008227.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Carcinoma Pulmonar de Células não Pequenas / Anticorpos Monoclonais Humanizados / Antineoplásicos Imunológicos / Neoplasias Pulmonares Tipo de estudo: Prognostic_studies Limite: Female / Humans / Male Idioma: En Revista: Lung Cancer Assunto da revista: NEOPLASIAS Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Carcinoma Pulmonar de Células não Pequenas / Anticorpos Monoclonais Humanizados / Antineoplásicos Imunológicos / Neoplasias Pulmonares Tipo de estudo: Prognostic_studies Limite: Female / Humans / Male Idioma: En Revista: Lung Cancer Assunto da revista: NEOPLASIAS Ano de publicação: 2019 Tipo de documento: Article