Skip to main content
Log in

Antitumoral Activity of Tyrosine Kinase Inhibitors in Patients with Non-small Cell Lung Cancer Harbouring Rare Epidermal Growth Factor Receptor Mutations

  • Short Communication
  • Published:
Molecular Diagnosis & Therapy Aims and scope Submit manuscript

Abstract

Introduction

Mutations in the epidermal growth factor receptor (EGFR) have been reported as predictive markers of tumour response to tyrosine kinase inhibitors (TKIs) in patients with non-small cell lung cancer (NSCLC). Although the “common” EGFR mutations have been associated with response to EGFR-TKIs, the correlation with response to treatment for many other rare mutations is still unclear. The aim of this study was to investigate the clinical significance of rare and complex mutations, and the efficacy of EGFR-TKIs in this selected group of patients.

Methods

Three hundred and thirty patients with stage IIIB/IV NSCLC (106 females aged 62.5 ± 1.1 years; 224 males aged 68.0 ± 0.6 years) were enrolled in the study. Formalin fixed paraffin embedded tissue samples were screened for mutations using a high resolution melting technique, followed by Sanger sequencing of exons 18-21 of the EGFR-gene. Mutation status was also tested using the Roche Cobas® EGFR mutation test.

Results

EGFR mutations were detected in 31 tumours (9.4 %). Eleven cases carried novel mutations, six of these patients were treated with erlotinib or gefitinib. A response rate (RR) of 50.0 % was obtained in the group with rare EGFR mutations, the PFS was 3.0 months [standard deviation (STD) = 5.4 months]. The RR to EGFR-TKIs in patients with conventional EGFR mutations was 85 % with a median PFS of 10.5 months (STD = 3.6 months).

Conclusion

We reported six patients with rare EGFR mutations of unknown clinical significance and their association with EGFR-TKIs. Report of cases harbouring rare mutations can support the decision making progress in this subset of patients.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

References

  1. Shigematsu H, Lin L, Takahashi T, et al. Clinical course of patients with epidermal growth factor receptor gene mutations in lung cancers. J Natl Cancer Inst. 2005;97:339–46.

    Article  CAS  PubMed  Google Scholar 

  2. Ferlay J. Cancer incidence and mortality patterns in Europe: estimates for 40 countries in 2012. Eur J Cancer. 2013;49:1374–403.

    Article  CAS  PubMed  Google Scholar 

  3. Mok TS, Wu YL, Thonprasert S, et al. Gefitinib or carboplatin-paclitaxel in pulmonary adenocarcinoma. N Engl J Med. 2009;361:947–57.

    Article  CAS  PubMed  Google Scholar 

  4. Pallis AG, Voutsina A, Kalikaki A, et al. ‘Classical’ but no ‘other’ mutations of EGFR kinase domain are associated with clinical outcome in gefitinib-treated patients with non-small cell lung cancer. Br J Cancer. 2007;17:3812–21.

    Google Scholar 

  5. Mitsudomi T, Morita S, Yatabe Y, et al. Gefitinib versus cisplatin plus docetaxel in patients with non-small cell lung cancer harbouring mutations of the epidermal growth factor receptor (WJTOG3405): an open label, randomized phase 3 trial. Lancet Oncol. 2010;11:121–8.

    Article  CAS  PubMed  Google Scholar 

  6. Riely GJ, Pao W, Pham D, et al. Clinical course of patients with non-small cell lung cancer and epidermal growth factor receptor exon 19 and exon 21 mutations treated with gefitinib or erlotinib. Clin Cancer Res. 2006;12:839–44.

    Article  CAS  PubMed  Google Scholar 

  7. Wu JY, Yu CJ, Yang CH, et al. First-or second-line therapy with gefitinib produces equal survival in non small cell lung cancer. Am J Respir Crit Care Med. 2008;178:847–53.

    Article  CAS  PubMed  Google Scholar 

  8. Murray S, Dahabreh IJ, Linardou H, et al. Somatic mutations of the tyrosine kinase domain of epidermal growth factor receptor and tyrosine kinase inhibitor response to TKI in non small cell lung cancer: an analytical database. J Thorac Oncol. 2008;3:832–9.

    Article  PubMed  Google Scholar 

  9. Gu D, Scaringe WA, Li K, et al. Database of somatic mutations in EGFR with analyses revealing indel hotspots but no smoking-associated signature. Human Mutat. 2007;28:760–70.

    Article  CAS  Google Scholar 

  10. De Pas T, Toffalorio F, Manzotti M, et al. Activity of Epidermal growth factor receptor tyrosine kinas inhibitors in patients with non small cell lung cancer harbouring rare epidermal growth factor receptor mutations. J Thorac Oncol. 2011;6:1895–901.

    Article  PubMed  Google Scholar 

  11. Ceteno I, Blay P, Santamaria I, et al. Germ-line mutations in epidermal growth factor receptor (EGFR) are rare but may contribute to oncgenesis: a novel germ line mutation in EGFR detected in a patient with lung adenocarcinoma. BMC Cancer. 2011;11:172.

    Article  Google Scholar 

  12. Travis WD, Brambilla E, Noguchi M, et al. International association for the study of lung cancer/American thoracic society/European respiratory society international multidisciplinary classification of lung adenocarcinoma. J Thorac Oncol. 2011;6:244–85.

    Article  PubMed Central  PubMed  Google Scholar 

  13. Do H, Krypuy M, Mitchell P, et al. High resolution melting analysis for rapid and sensitive EGFR and KRAS mutation detection in formalin fixed paraffin embedded biopsies. BMC Cancer. 2008;8:142.

    Article  PubMed Central  PubMed  Google Scholar 

  14. Heideman D, Thunnissen F, Doeleman M, et al. A panel of high resolution melting (HRM) technology-based assays with direct sequencing possibility for effective mutation screening of EGFR and K-ras genes. Cell Oncol. 2009;31:329–33.

    CAS  PubMed  Google Scholar 

  15. Eisenhauer EA, Therasse P, Bogaerts J, et al. New response evaluation criteria in solid tumours: revised RECIST guiline (version 1.1). Eur J Cancer. 2009;2:228–47.

    Article  Google Scholar 

  16. Vallières E, Shepherd FA, Crowley J, et al. The IASLC lung cancer staging project: proposals regarding the relevance of TNM in the pathologic staging of small cell lung cancer in the forthcoming (seventh) edition of the TNM classification for lung cancer. J Thorac Oncol. 2009;2009(4):1049–59.

    Article  Google Scholar 

  17. Chan SK, Gullick WJ, Hill ME. Mutations of the epidermal growth factor receptor in non-small cell lung cancersearch and destroy. Eur J Cancer. 2006;42:17–23.

    Article  CAS  PubMed  Google Scholar 

  18. Hiesh MH, Fang YF, Chang WC, et al. Complex mutation patterns of epidermal growth factor receptor gene associated with variable responses to gefitinib treatment in patients with non-small cell lung cancer. Lung Cancer. 2006;53:311–22.

    Article  Google Scholar 

  19. Takano T, Ohe Y, Sakamoto H, et al. Epidermal growth factor receptor gene mutations and increased copy numbers predict gefitinib sensitivity in patients with recurrent non-small cell lung cancer. J Clin Oncol. 2005;23:6829–37.

    Article  CAS  PubMed  Google Scholar 

  20. Ichihara S, Toyooka S, Fujiwara Y, et al. The impact of epidermal growth factor receptor gene status on gefitinib-treated Japanese patients with non-small cell lung cancer. Int J Cancer. 2007;120:1239–47.

    Article  CAS  PubMed  Google Scholar 

  21. De Vries NA, Buckle T, Zhao J, et al. Restricted brain penetration of the tyrosine kinase inhibitor erlotinib due to the drug transportersP-gp and BCRP. Invest New Drugs. 2012;30:443–9.

    Article  CAS  PubMed  Google Scholar 

  22. Balak MN, Gong Y, Riely GJ, et al. Novel D761Y and common secondary T790 M mutations in epidermal growth factor receptor mutatant lung adenocarcinomas with acquired resistance to kinase inhibitors. Clin Cancer Res. 2006;12:6494–501.

    Article  CAS  PubMed  Google Scholar 

  23. Mao C, Qiu LX, Liao RY, et al. KRAS mutations and resistance to EGFR-TKIs treatment in patients with non-small cell lung cancer: a meta-analysis of 22 studies. Lung Cancer. 2010;69:272–8.

    Article  PubMed  Google Scholar 

  24. Kimura H, Suminoe M, Kasahara K, et al. Evaluation of epidermal growth factor receptor mutation status in serum DNA as a predictor of response to gefitinib (IRESSA). Br J Cancer. 2007;97:778–84.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  25. Rios FL, Angulo B, Gomez B, et al. Comparison of molecular testing methods for the detection of EGFR mutations in formalin-fixed paraffin-embedded tissue specimens of non-small cell lung cancer. J Clin Pathol. 2013;66:381–5.

    Article  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Matthijs Oyaert.

Ethics declarations

Conflict of interest

MO, ID, ED, FD, JV, EDL and JB have no conflicts of interest to report.

Funding

MO, ID, ED, FD, JV, EDL and JB have no sources of funding to report.

Ethical approval and informed consent

The authors state that this study was performed with full respect for individuals’ rights to confidentiality and in accordance with procedures supervised by local authorities responsible for ethical research.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Oyaert, M., Demedts, I., Boone, E. et al. Antitumoral Activity of Tyrosine Kinase Inhibitors in Patients with Non-small Cell Lung Cancer Harbouring Rare Epidermal Growth Factor Receptor Mutations. Mol Diagn Ther 19, 267–272 (2015). https://doi.org/10.1007/s40291-015-0158-z

Download citation

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s40291-015-0158-z

Keywords

Navigation