Literature DB >> 17382026

Epidermal growth factor receptor inhibitors plus chemotherapy in non-small-cell lung cancer: biologic rationale for combination strategies.

David R Gandara1, Angela M Davies, Oliver Gautschi, Philip C Mack, Derick H Lau, Primo N Lara, Fred R Hirsch.   

Abstract

Chemotherapy continues to play an essential role in the treatment of most stages of non-small-cell lung cancer (NSCLC). In fact, within the past 5 years, this role has greatly expanded into adjuvant therapy for early-stage resected disease. Likewise, agents targeting the epidermal growth factor receptor (EGFR), particularly the tyrosine kinase inhibitors gefitinib and erlotinib, have proven to be clinically active in patients with advanced-stage NSCLC. Because of these findings, it is logical to expect that combinations of these 2 classes of antineoplastic agents would prove more efficacious than either one alone. Yet 4 large randomized phase III trials of chemotherapy with or without an EGFR tyrosine kinase inhibitor in unselected patients with advanced-stage NSCLC, altogether totaling > 4000 patients, did not demonstrate improvement in clinical outcomes with the combination. Whether these negative results will be reproduced in ongoing combination studies of chemotherapy plus monoclonal antibodies directed against EGFR remain to be determined. Herein, we review recent preclinical and clinical data addressing this topic and explore the biologic rationale for developing new combination strategies based on patient selection by molecular and clinical factors, or by pharmacodynamic parameters.

Entities:  

Mesh:

Substances:

Year:  2007        PMID: 17382026     DOI: 10.3816/clc.2007.s.003

Source DB:  PubMed          Journal:  Clin Lung Cancer        ISSN: 1525-7304            Impact factor:   4.785


  6 in total

1.  Phase II selection design trial of concurrent chemotherapy and cetuximab versus chemotherapy followed by cetuximab in advanced-stage non-small-cell lung cancer: Southwest Oncology Group study S0342.

Authors:  Roy S Herbst; Karen Kelly; Kari Chansky; Philip C Mack; Wilbur A Franklin; Fred R Hirsch; James N Atkins; Shaker R Dakhil; Kathy S Albain; Edward S Kim; Mary Redman; John J Crowley; David R Gandara
Journal:  J Clin Oncol       Date:  2010-10-04       Impact factor: 44.544

2.  EGFR Inhibition in the Treatment of Non-Small Cell Lung Cancer.

Authors:  David E Gerber
Journal:  Drug Dev Res       Date:  2008-12-09       Impact factor: 4.360

3.  Intercalated erlotinib-docetaxel dosing schedules designed to achieve pharmacodynamic separation: results of a phase I/II trial.

Authors:  Randeep Sangha; Angela M Davies; Primo N Lara; Philip C Mack; Laurel A Beckett; Paul J Hesketh; Derick Lau; Tianhong Li; Natasha Perkins; David R Gandara
Journal:  J Thorac Oncol       Date:  2011-12       Impact factor: 15.609

4.  Schedule-dependent synergistic interaction between docetaxel and gefitinib in NSCLC cell lines regardless of the mutation status of EGFR and KRAS and its molecular mechanisms.

Authors:  Yanwen Jiang; Qing Yuan; Qiuhong Fang
Journal:  J Cancer Res Clin Oncol       Date:  2014-04-13       Impact factor: 4.553

Review 5.  [Optimal therapeutic strategy for non-small cell lung cancer with mutated epidermal growth factor receptor].

Authors:  Zhong Shi; Yun Fan
Journal:  Zhongguo Fei Ai Za Zhi       Date:  2015-02

6.  Clinical study on gefitinib combined with γ-ray stereotactic body radiation therapy as the first-line treatment regimen for senile patients with adenocarcinoma of the lung (final results of JLY20080085).

Authors:  Dejian Pan; Biao Wang; Xijian Zhou; Donglin Wang
Journal:  Mol Clin Oncol       Date:  2013-05-27
  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.