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Author
- Adeni, Anika E1
- Antonia, Scott1
- Awad, Mark M1
- Baas, Paul1
- Babu, Sunil1
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- Borghaei, Hossein1
- Brahmer, Julie R1
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- Burgers, Sjaak1
- Chandler, Jason1
- Cheng, Matthew P1
- Chow, Laura QM1
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- Dong, Hui1
- Faig, Jennifer1
- Garon, Edward B1
- Geese, William J1
- Gerber, David E1
- Gettinger, Scott1
- Goldman, Jonathan W1
- Hammond, Sarah P1
- Hartemink, Koen1
- Hellmann, Matthew D1
Keyword
- Immunotherapy2
- Advanced NSCLC1
- anaplastic lymphoma kinase translocation1
- Checkpoint inhibitor1
- Clinical benefit1
- Combination therapy1
- Crizotinib1
- EGFR-mutant NSCLC1
- Erlotinib1
- Gut microbiota1
- HIV1
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- PD-11
- PD-1 inhibitor1
- PD-L11
- Pembrolizumab1
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- Programmed death ligand 11
- Systemic immune signatures1
Editors Choice
5 Results
- Original Article Translational OncologyOpen Archive
The Diversity of Gut Microbiome is Associated With Favorable Responses to Anti–Programmed Death 1 Immunotherapy in Chinese Patients With NSCLC
Journal of Thoracic OncologyVol. 14Issue 8p1378–1389Published online: April 23, 2019- Yueping Jin
- Hui Dong
- Liliang Xia
- Yi Yang
- Yongqiang Zhu
- Yan Shen
- and others
Cited in Scopus: 195Gut microbiome affecting the responses to immune checkpoint inhibitors against advanced NSCLC has been investigated in the Western population. However, considering pre-existing genetic and gut microbiota variation, the relevance remains unknown in the East-Asian NSCLC population. This study is designed to explore the relationship between gut microbiome and clinical outcomes in Chinese patients with NSCLC who have received treatment using an anti–programmed death 1 (PD-1) blockade. - Original Article MesotheliomaOpen Access
Programmed Death 1 Blockade With Nivolumab in Patients With Recurrent Malignant Pleural Mesothelioma
Journal of Thoracic OncologyVol. 13Issue 10p1569–1576Published online: June 13, 2018- Josine Quispel-Janssen
- Vincent van der Noort
- Jeltje F. de Vries
- Marion Zimmerman
- Ferry Lalezari
- Erik Thunnissen
- and others
Cited in Scopus: 160Malignant pleural mesothelioma (MPM) has limited treatment options and a poor outcome. Programmed death 1/programmed death ligand 1 (PD-L1) checkpoint inhibitors have proven efficacious in several cancer types. Nivolumab is a fully humanized monoclonal antibody against programmed death 1 with a favorable toxicity profile. In MPM, the immune system is considered to play an important role. We therefore tested nivolumab in recurrent MPM. - Original Article Non–Small Cell Lung CancerOpen Archive
Nivolumab Plus Erlotinib in Patients With EGFR-Mutant Advanced NSCLC
Journal of Thoracic OncologyVol. 13Issue 9p1363–1372Published online: May 23, 2018- Scott Gettinger
- Matthew D. Hellmann
- Laura Q.M. Chow
- Hossein Borghaei
- Scott Antonia
- Julie R. Brahmer
- and others
Cited in Scopus: 116This phase I study evaluated nivolumab combined with erlotinib in patients with advanced EGFR-mutant NSCLC. - Brief ReportOpen Archive
Safety and Efficacy of PD-1 Inhibitors Among HIV-Positive Patients With Non–Small Cell Lung Cancer
Journal of Thoracic OncologyVol. 13Issue 7p1037–1042Published online: April 6, 2018- Lorena Ostios-Garcia
- Jennifer Faig
- Giulia C. Leonardi
- Anika E. Adeni
- Safiya J. Subegdjo
- Christine A. Lydon
- and others
Cited in Scopus: 69Despite widespread administration of programmed death receptor 1 (PD-1) pathway inhibitors among individuals with NSCLC, little is known about the safety and activity of these agents among human immunodeficiency virus (HIV) – infected patients since this population has largely been excluded from immunotherapy clinical trials. - Original Article Non–Small Cell Lung CancerOpen Archive
Phase 1/2 Study of the Safety and Tolerability of Nivolumab Plus Crizotinib for the First-Line Treatment of Anaplastic Lymphoma Kinase Translocation — Positive Advanced Non–Small Cell Lung Cancer (CheckMate 370)
Journal of Thoracic OncologyVol. 13Issue 5p682–688Published online: March 5, 2018- David R. Spigel
- Craig Reynolds
- David Waterhouse
- Edward B. Garon
- Jason Chandler
- Sunil Babu
- and others
Cited in Scopus: 157Crizotinib, an anaplastic lymphoma kinase (ALK) inhibitor, is a first-line treatment for ALK translocation–positive advanced non–small cell lung cancer (NSCLC); however, patients eventually progress. Immunotherapies, including the programmed death-1 inhibitor nivolumab, have resulted in durable responses and long-term overall survival in patients with NSCLC. We hypothesized that combining targeted therapy with immunotherapy could result in more patients with responses and/or more durable responses.