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- Bar, Jair2
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Editors Choice
3 Results
- Original Article Non-Small Cell Lung CancerOpen Access
Treatment Characteristics and Real-World Progression-Free Survival in Patients With Unresectable Stage III NSCLC Who Received Durvalumab After Chemoradiotherapy: Findings From the PACIFIC-R Study
Journal of Thoracic OncologyVol. 18Issue 2p181–193Published online: October 24, 2022- Nicolas Girard
- Jair Bar
- Pilar Garrido
- Marina C. Garassino
- Fiona McDonald
- Françoise Mornex
- and others
Cited in Scopus: 4The phase 3 PACIFIC trial established consolidation therapy with durvalumab as standard of care for patients with unresectable, stage III NSCLC and no disease progression after definitive chemoradiotherapy (CRT). The observational PACIFIC-R study assesses the real-world effectiveness of durvalumab in patients from an early access program. Here, we report treatment characteristics and a preplanned analysis of real-world progression-free survival (rwPFS). - Original Article Non-Small Cell Lung CancerOpen Access
UNcommon EGFR Mutations: International Case Series on Efficacy of Osimertinib in Real-Life Practice in First-LiNe Setting (UNICORN)
Journal of Thoracic OncologyVol. 18Issue 2p169–180Published online: October 24, 2022- Jair Bar
- Nir Peled
- Shiruyeh Schokrpur
- Mirjana Wolner
- Ofer Rotem
- Nicolas Girard
- and others
Cited in Scopus: 3Approximately 10% of EGFR mutations (EGFRmuts) are uncommon (ucEGFRmuts). We aimed to collect real-world data about osimertinib for patients with ucEGFRmuts. - Editorial
EGFR Tyrosine Kinase Inhibitor Sequencing Revisited: From the Revival of Old Tools to the Integration of New Agents
Journal of Thoracic OncologyVol. 17Issue 9p1067–1069Published in issue: September, 2022- Nicolas Girard
Cited in Scopus: 0In this issue of the Journal of Thoracic Oncology, Piccirillo et al.1 report the results of the BEVERLY trial, a randomized phase 3 study that reveals the progression-free survival (PFS) benefit of bevacizumab to erlotinib as first-line treatment for Italian patients with metastatic NSCLC with common EGFR mutations. In this large study, after a median follow-up of 36.3 months, median investigator-assessed PFS was 15.4 months with erlotinib plus bevacizumab and 9.6 months with erlotinib alone (hazard ratio = 0.66, 95% confidence interval: 0.47–0.92).