Erlotinib versus standard chemotherapy as first-line treatment for European patients with advanced EGFR mutation-positive non-small-cell lung cancer (EURTAC): a multicentre, open-label, randomised…
By R. Rosell, E. Carcereny, R. Gervais, A. Vergnenègre, B. Massutí, E. Felip, R. Palmero, R. García-Gómez, C. Pallarés, J. Sánchez and 47 more. The Lancet Oncology, 2012
5,252 citations recorded by the source corpus.
Subfields: Oncology, Pulmonary and Respiratory Medicine
View Paper: https://www.semanticscholar.org/paper/b925e8cfc1a2df68d3c4af1a5af416aa9a16ad06
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Citations in the corpus
- AZD9291 in EGFR inhibitor-resistant non-small-cell lung cancer. (2015, neutral): “Any grade 5 (24) 5 (9) 9 (10) 5 (8) 1 (5) 25 (10)”
- Clinical Experience With Crizotinib in Patients With Advanced ALK-Rearranged Non-Small-Cell Lung Cancer and Brain Metastases. (2015, background): “These latter numbers are not dissimilar from data available for other oncogene-driven NSCLCs treated with TKIs, such as epidermal growth factor receptor (EGFR) –mutated NSCLC treated with gefitinib or erlotinib.(32,33) In one report of EGFR-mutated NSCLC, the cumulative incidence of brain metastases”
- A standardised, generic, validated approach to stratify the magnitude of clinical benefit that can be anticipated from anti-cancer therapies: the European Society for Medical Oncology Magnitude of Clinical Benefit Scale (ESMO-MCBS). (2015, background): “5 mth NS 15% less severe adverse reactions 4 [76]”
- Rociletinib in EGFR-mutated non-small-cell lung cancer. (2015, neutral): “Decreased appetite 19 (15) 1 (3) 6 (32) 4 (24) 3 (19) 3 (9) 2 (33) 18 (20)”