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. 2010 May 25:4:81-98.
doi: 10.2147/dddt.s6594.

Emerging role of gefitinib in the treatment of non-small-cell lung cancer (NSCLC)

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Emerging role of gefitinib in the treatment of non-small-cell lung cancer (NSCLC)

M Tiseo et al. Drug Des Devel Ther. .

Abstract

Most patients with non-small-cell lung cancer (NSCLC) present with advanced disease and their long-term prognosis remains poor. Epidermal growth factor receptor (EGFR)-targeted therapies, such as gefitinib, have been subjected to comprehensive clinical development. Several phase II and III trials evaluated the clinical efficacy of gefitinib as monotherapy in pretreated patients with advanced NSCLC, as well as both monotherapy and combined with chemotherapy in chemotherapy-naive patients. A phase III trial (ISEL) in heavily pretreated advanced NSCLC patients demonstrated some improvement in survival with gefitinib compared with placebo; however, the difference was not statistically significant within the overall population. A large phase III trial in pretreated patients (INTEREST) demonstrated the non-inferiority of gefitinib in comparison with docetaxel for overall survival, together with an improved quality of life and tolerability profiles. In a large phase III trial (IPASS) in Asian chemotherapy-naive, never or former light-smoker patients with adenocarcinoma, gefitinib was more effective than carboplatin-paclitaxel in prolonging progression-free survival, particularly in patients harboring EGFR gene mutations. Gefitinib was a generally well tolerated treatment, with skin rash and diarrhea being the most common treatment adverse events. As a result, gefitinib is expected to have a large impact on the management of patients with advanced NSCLC, in particular in EGFR mutated patients.

Keywords: EGFR; gefitinib; non-small-cell lung cancer.

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Figures

Figure 1
Figure 1
Progression-free survival (PFS) and overall survival (OS) results (months) obtained with gefitinib in EGFR biomarker subgroups of ISEL and INTEREST trials., Abbreviations: PFS, progression-free survival; OS, overall survival; NA, not available; IHC, immunohistochemistry; EGFR FISH positive, high gene copy number; EGFR FISH negative, low gene copy number
Figure 2
Figure 2
Progression-free survival (PFS) results (months) in EGFR mutated subgroups in IPASS, First-SIGNAL, WJTOG3405 and NEJ002 trials.– Abbreviations: NA, not available; EGFR FISH positive, high gene copy number; EGFR FISH negative, low gene copy number.

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References

    1. Jemal A, Siegel R, Ward E, Hao Y, Xu J, Thun MJ. Cancer Statistics, 2009. CA Cancer J Clin. 2009;59(4):225–249. - PubMed
    1. Travis WD, Brambilla E, Müller-Hermelink HK, Harris CC. Pathology and genetics of tumors of the lung, pleura, thymus and heart. In: Kleihues P, Sobin LH, editors. WHO Classification of Tumors. Lyon: IARC press; 2004.
    1. Non Small Cell Lung Cancer Collaborative Group. Chemotherapy in non-small cell lung cancer: a meta-analysis using update data on individual patients from 52 randomised clinical trials. BMJ. 1995;311(7010):899–909. - PMC - PubMed
    1. NSCLC Meta-Analyses Collaborative Group. Chemotherapy in addition to supportive care improves survival in advanced non-small-cell-lung cancer: a systematic review and meta-analysis of individual patients data from 16 randomized controlled trials. J Clin Oncol. 2008;26(28):4617–4625. - PMC - PubMed
    1. Waters JS, O’Brien MER. The case for the introduction of new chemotherapy agents in the treatment of advanced non-small cell lung cancer in the wake of the findings of The National Institute of Clinical Excellence (NICE) Br J Cancer. 2002;87(5):481–490. - PMC - PubMed

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