Efficacy and safety of sunitinib in patients with advanced gastrointestinal stromal tumour after failure of imatinib: a randomised controlled trial.
By G. Demetri, A. van Oosterom, C. Garrett, M. Blackstein, M. Shah, J. Verweij, G. McArthur, I. Judson, M. Heinrich, J. Morgan and 7 more. The Lancet, 2006
2,477 citations recorded by the source corpus.
Subfields: Gastroenterology, Surgery
View Paper: https://www.semanticscholar.org/paper/0c0c1c281a38ef2833642a2e542ef85d7d4e6507
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Citations in the corpus
- The crucial role of protein phosphorylation in cell signaling and its use as targeted therapy (Review) (2017, neutral): “Many of these kinases are now considered cancer biomarkers, such as EGFR for colon cancer, cKIT for GISTs, and human EGFR-related gene (Her2) for breast cancer (112).”
- Molecular basis for sunitinib efficacy and future clinical development (2007, background): “cgi?id=606764">gastrointestinal stromal tumours (GIST) that are refractory or intolerant to imatini”
- 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, neutral): “33 (0·23–0·47) 3 [134]”
- Dissecting therapeutic resistance to RAF inhibition in melanoma by tumor genomic profiling. (2011, background): “proved for use in imatinib-refractory GIST.(26,107) Although the aforementioned”
- Gastrointestinal stromal tumours: origin and molecular oncology (2011, background): “Sunitinib is US Food and Drug Administration (FDA)-approved for the treatment of patients with GISTs with progression on imatini”