Literature DB >> 16330289

Erlotinib: small-molecule targeted therapy in the treatment of non-small-cell lung cancer.

Janine Smith1.   

Abstract

BACKGROUND: Erlotinib is an oral tyrosine kinase inhibitor, targeting the human epidermal receptor type 1/ epidermal growth factor receptor, recently approved by the US Food and Drug Administration (FDA) for the treatment of patients with locally advanced or metastatic non-small-cell lung cancer (NSCLC) after the failure of more than 1 or 2 previous chemotherapeutic regimens.
OBJECTIVE: The purpose of this article is to summarize the development, pharmacology, pharmacokinetics, efficacy, and adverse effects of erlotinib.
METHODS: A literature search was conducted with the MEDLINE and EMBASE (1999-2005) databases using the search terms non-small-cell lung cancer, erlotinib, and epidermal growth factor receptor inhibitor. Abstracts from the American Society of Clinical Oncology and documents submitted to the FDA also were reviewed.
RESULTS: BR.21, a randomized, placebo-controlled, multinational Phase III trial demonstrated clinically and statistically improved overall survival in patients with advanced or metastatic NSCLC treated with erlotinib versus placebo as second-line therapy. The erlotinib group had a median survival of 6.7 months versus a median survival of 4.7 months in the placebo group (P < 0.001). The toxicity profile of erlotinib was moderately benign, with the most commonly documented adverse events requiring dose reductions including skin rash (12%) and diarrhea (5%). Interstitial lung disease and relative fatalities were reported infrequently (0.8%) in patients receiving erlotinib. Two randomized, placebo-controlled, multicenter Phase III trials conducted in patients with locally advanced and metastatic NSCLC showed no clinical benefit with first-line administration of erlotinib plus concurrent platinum-based chemotherapy.
CONCLUSIONS: For patients with NSCLC in whom more than 1 or 2 previous chemotherapeutic regimens have failed, erlotinib is an effective therapy with significant overall survival benefits. The use of erlotinib as first-line therapy in combination with platinum-based chemotherapeutic regimens, however, has failed to demonstrate efficacy in the treatment of NSCLC.

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Year:  2005        PMID: 16330289     DOI: 10.1016/j.clinthera.2005.10.014

Source DB:  PubMed          Journal:  Clin Ther        ISSN: 0149-2918            Impact factor:   3.393


  25 in total

Review 1.  Emerging treatments and gene expression profiling in high-risk medulloblastoma.

Authors:  Iacopo Sardi; Duccio Cavalieri; Maura Massimino
Journal:  Paediatr Drugs       Date:  2007       Impact factor: 3.022

2.  Inhibition of the epidermal growth factor receptor by erlotinib prevents immortalization of human cervical cells by Human Papillomavirus type 16.

Authors:  Craig D Woodworth; Laura P Diefendorf; David F Jette; Abdulmajid Mohammed; Michael A Moses; Sylvia A Searleman; Dan A Stevens; Katelynn M Wilton; Sumona Mondal
Journal:  Virology       Date:  2011-10-05       Impact factor: 3.616

3.  Investigating Molecular Mechanisms of Activation and Mutation of the HER2 Receptor Tyrosine Kinase through Computational Modeling and Simulation.

Authors:  Shannon E Telesco; Andrew Shih; Yingting Liu; Ravi Radhakrishnan
Journal:  Cancer Res J       Date:  2011

4.  Phase Ib Study of Chemoprevention with Green Tea Polyphenon E and Erlotinib in Patients with Advanced Premalignant Lesions (APL) of the Head and Neck.

Authors:  Dong M Shin; Sreenivas Nannapaneni; Mihir R Patel; Qiuying Shi; Yuan Liu; Zhengjia Chen; Amy Y Chen; Mark W El-Deiry; Jonathan J Beitler; Conor E Steuer; Steven M Roser; Adam M Klein; Taofeek K Owonikoko; Suresh S Ramalingam; Fadlo R Khuri; Zhuo G Chen; Nabil F Saba
Journal:  Clin Cancer Res       Date:  2020-09-17       Impact factor: 12.531

5.  The UGT1A1*28 polymorphism correlates with erlotinib's effect on SN-38 glucuronidation.

Authors:  Yong Liu; Jacqueline Ramírez; Larry House; Mark J Ratain
Journal:  Eur J Cancer       Date:  2010-05-23       Impact factor: 9.162

6.  Substrate-dependent modulation of the catalytic activity of CYP3A by erlotinib.

Authors:  Pei-pei Dong; Zhong-ze Fang; Yan-yan Zhang; Guang-bo Ge; Yu-xi Mao; Liang-liang Zhu; Yan-qing Qu; Wei Li; Li-ming Wang; Chang-xiao Liu; Ling Yang
Journal:  Acta Pharmacol Sin       Date:  2011-03       Impact factor: 6.150

7.  Modified synthesis of erlotinib hydrochloride.

Authors:  Leila Barghi; Ayuob Aghanejad; Hadi Valizadeh; Jaleh Barar; Davoud Asgari
Journal:  Adv Pharm Bull       Date:  2012-05-05

8.  Proton MRS detects metabolic changes in hormone sensitive and resistant human prostate cancer models CWR22 and CWR22r.

Authors:  H Carl Le; Mihaela Lupu; Khushali Kotedia; Neal Rosen; David Solit; Jason A Koutcher
Journal:  Magn Reson Med       Date:  2009-11       Impact factor: 4.668

9.  Antitumor activity of a novel EGFR tyrosine kinase inhibitor against human lung carcinoma in vitro and in vivo.

Authors:  Xishan Xiong; Lili Fu; Li Wang; Houan Cai; Lin Li; Hualiang Jiang; Wenhu Duan; Changlin Mei
Journal:  Invest New Drugs       Date:  2008-05-21       Impact factor: 3.850

10.  Comparison of the drug-drug interactions potential of erlotinib and gefitinib via inhibition of UDP-glucuronosyltransferases.

Authors:  Yong Liu; Jacqueline Ramírez; Larry House; Mark J Ratain
Journal:  Drug Metab Dispos       Date:  2010-01       Impact factor: 3.922

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