ZD1839, a selective oral epidermal growth factor receptor-tyrosine kinase inhibitor, is well tolerated and active in patients with solid, malignant tumors: results of a phase I trial.
By M. Ranson, L. Hammond, D. Ferry, M. Kris, A. Tullo, P. Murray, Vincent A. Miller, S. Averbuch, J. Ochs, C. Morris and 3 more. Journal of Clinical Oncology, 2002
788 citations recorded by the source corpus.
Subfields: Oncology, Pulmonary and Respiratory Medicine
View Paper: https://www.semanticscholar.org/paper/7be248b64576ef1eefe7a0e8e802ca1b6ecae54b
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Citations in the corpus
- Clinical signs, pathophysiology and management of skin toxicity during therapy with epidermal growth factor receptor inhibitors. (2005, background): “The rash seems to be dosedependent [4, 11, 12, 14 , 17] and is seen in more than 50% up to 100% of patients (Table 1). Further studies are ongoing to understand this dose relationship better.”
- Gefitinib in combination with paclitaxel and carboplatin in advanced non-small-cell lung cancer: a phase III trial--INTACT 2. (2004, background): “Four phase I studies have shown that gefitinib is generally well tolerated, with evidence of antitumor activity in a range of tumors including NSCLC [5-8].”
- Bronchioloalveolar pathologic subtype and smoking history predict sensitivity to gefitinib in advanced non-small-cell lung cancer. (2004, methodology): “Three phase I trials have been reported [3-5], and in two of these major objective responses were observed in patients with NSCLC refractory to multiple From the Thoracic Oncology Service,”
- Role of Tyrosine Kinase Inhibitors in Cancer Therapy (2005, background): “Headache, mucositis, hyperbilirubinemia, neutropenia, and anemia have also been reported (Ranson et al., 2002; Ranson, 2004).”
- Phase II trial of gefitinib in recurrent glioblastoma. (2004, background): “As expected, the most common toxicities were rash and diarrhea [9-11,26].”