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Efficacy of Gefitinib, an Inhibitor of the Epidermal Growth Factor Receptor Tyrosine Kinase, in Symptomatic Patients With Non-Small Cell Lung Cancer

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TLDR
Gefitinib, a well-tolerated oral EGFR-tyrosine kinase inhibitor, improved disease-related symptoms and induced radiographic tumor regressions in patients with NSCLC persisting after chemotherapy as mentioned in this paper.
Abstract
Results Of 221 patients enrolled, 216 received gefitinib as randomized. Symptoms of NSCLC improved in 43% (95% confidence interval [CI], 33%-53%) of patients receiving 250 mg of gefitinib and in 35% (95% CI, 26%-45%) of patients receiving 500 mg. These benefits were observed within 3 weeks in 75% of patients. Partial radiographic responses occurred in 12% (95% CI, 6%-20%) of individuals receiving 250 mg of gefitinib and in 9% (95% CI, 4%-16%) of those receiving 500 mg. Symptoms improved in 96% of patients with partial radiographic responses. The overall survival at 1 year was 25%. There were no significant differences between the 250-mg and 500-mg doses in rates of symptom improvement (P=.26), radiographic tumor regression (P=.51), and projected 1-year survival (P=.54). The 500-mg dose was associated more frequently with transient acne-like rash (P=.04) and diarrhea (P=.006). Conclusions Gefitinib, a well-tolerated oral EGFR-tyrosine kinase inhibitor, improved disease-related symptoms and induced radiographic tumor regressions in patients with NSCLC persisting after chemotherapy.

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EGFR-targeted therapies in lung cancer: predictors of response and toxicity

TL;DR: The current state of knowledge of predictors of response and toxicity to EGFR inhibitors in lung cancer is reviewed, including tumor-related molecular markers, as well as germline markers such as polymorphisms in EGFR or EGFR pathway-related genes.
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Gefitinib vs. chemotherapy as first-line therapy in advanced non-small cell lung cancer: Meta-analysis of phase III trials

TL;DR: A meta-analysis of four randomized studies that compared gefitinib with chemotherapy in the first-line treatment of patients with advanced NSCLC confirmed the results of each individual study and narrows the confidence intervals of these results.
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Methylation of the candidate biomarker TCF21 is very frequent across a spectrum of early-stage nonsmall cell lung cancers.

TL;DR: The transcription factor TCF21 is involved in mesenchymal‐to‐epithelial differentiation and was shown to be aberrantly hypermethylated in lung and head and neck cancers and its reported high frequency of hypermethylation was assessed.
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Polymorphisms of EGFR predict clinical outcome in advanced non-small-cell lung cancer patients treated with Gefitinib.

TL;DR: The D994D and CA-SSR polymorphisms in EGFR are potential predictors for clinical outcome in advanced NSCLC patients treated with Gefitinib.
Journal ArticleDOI

Targeting EGFR in non-small-cell lung cancer: lessons, experiences, strategies.

TL;DR: This review analyses the current state of the art of molecularly-tailored pharmacological approach to lung cancer, addressed to genetic lesions activating the EGFR pathway transducers, focusing on their role as markers of targeted drug response.
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