Literature DB >> 26961971

The Use of EGFR Tyrosine Kinase Inhibitors in EGFR Wild-Type Non-Small-Cell Lung Cancer.

Thomas E Stinchcombe1.   

Abstract

The objective response rate and progression-free survival observed with epidermal growth factor receptor tyrosine kinase inhibitors (EGFR TKIs) in patients with metastatic epidermal growth factor receptor (EGFR) wild-type non-small cell lung cancer (NSCLC) are modest. The adverse events associated with EGFR TKIs are manageable but they must be considered in the context of the limited efficacy. The development of anti-PD-1 immunotherapy as second-line therapy has reduced the role of EGFR TKIs in EGFR wild-type NSCLC. Recently, there has been increased recognition of the benefit of the earlier integration of palliative care and symptom management, and this is reasonable alternative to treatment with an EGFR TKI for many patients. My practice pattern for patients with EGFR wild-type NSCLC is platinum-based chemotherapy as first-line therapy, immunotherapy as second-line therapy, and single-agent chemotherapy as third-line therapy for patients with preserved performance status who want to pursue further therapy. Only a small proportion of patients are eligible for fourth-line therapy, and I prefer to enroll them in clinical trials rather than use EGFR TKIs. I suspect that the use of EGFR TKIs in clinical use and as a comparator arm for clinical trials will continue to decline over the next several years.

Entities:  

Keywords:  Biomarkers; EGFR wild-type; Molecular selection; Squamous; Targeted therapy

Mesh:

Substances:

Year:  2016        PMID: 26961971     DOI: 10.1007/s11864-016-0394-4

Source DB:  PubMed          Journal:  Curr Treat Options Oncol        ISSN: 1534-6277


  44 in total

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4.  Detection of tumor epidermal growth factor receptor pathway dependence by serum mass spectrometry in cancer patients.

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8.  Nivolumab versus Docetaxel in Advanced Nonsquamous Non-Small-Cell Lung Cancer.

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9.  Phase I trial of erlotinib-based multimodality therapy for inoperable stage III non-small cell lung cancer.

Authors:  Nicholas W Choong; Ann M Mauer; Daniel J Haraf; Eric Lester; Philip C Hoffman; Mark Kozloff; Shang Lin; Janet E Dancey; Livia Szeto; Tatyana Grushko; Olufunmilayo I Olopade; Ravi Salgia; Everett E Vokes
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10.  Adding Erlotinib to Chemoradiation Improves Overall Survival but Not Progression-Free Survival in Stage III Non-Small Cell Lung Cancer.

Authors:  Ritsuko Komaki; Pamela K Allen; Xiong Wei; George R Blumenschein; Ximing Tang; J Jack Lee; James W Welsh; Ignacio I Wistuba; Diane D Liu; Waun Ki Hong
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  11 in total

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3.  Pemetrexed-carboplatin with intercalated icotinib in the treatment of patient with advanced EGFR wild-type lung adenocarcinoma: A case report.

Authors:  Tongpeng Xu; Hao Wu; Shidai Jin; Huang Min; Zhihong Zhang; Yongqian Shu; Wei Wen; Renhua Guo
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4.  Incidence and risk of hepatic toxicities associated with anaplastic lymphoma kinase inhibitors in the treatment of non-small-cell lung cancer: a systematic review and meta-analysis.

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5.  Pathways and cost-effectiveness of routine lung cancer inpatient care in rural Anhui, China: a retrospective cohort study protocol.

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6.  Complete response associated with immune checkpoint inhibitors in advanced non-small-cell lung cancer: a meta-analysis of nine randomized controlled trials.

Authors:  Jie Li; Qi He; Xiu Yu; Khalid Khan; Xuanwen Weng; Minjie Guan
Journal:  Cancer Manag Res       Date:  2019-02-18       Impact factor: 3.989

7.  The serum-based VeriStrat® test is associated with proinflammatory reactants and clinical outcome in non-small cell lung cancer patients.

Authors:  Mary Jo Fidler; Cristina L Fhied; Joanna Roder; Sanjib Basu; Selina Sayidine; Ibtihaj Fughhi; Mark Pool; Marta Batus; Philip Bonomi; Jeffrey A Borgia
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8.  Involvement of GLUT1-mediated glucose transport and metabolism in gefitinib resistance of non-small-cell lung cancer cells.

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Review 10.  Salvage anlotinib showed sustained efficacy in heavily pretreated EGFR wild-type lung adenocarcinoma: A case report and review of the literature.

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