Literature DB >> 24342286

The role of molecular analyses in the diagnosis and treatment of non-small-cell lung carcinomas.

Giulio Rossi1, Paolo Graziano2, Alvaro Leone2, Mario Migaldi3, Raffaele Califano4.   

Abstract

Non-small-cell lung cancer (NSCLC) subtyping has recently been a key factor in determining patient management with novel drugs. In addition, the identification of distinct oncogenic driver mutations frequently associated with NSCLC histotype and coupled to the clinical responses to targeted therapies have revolutionized the impact of histologic type and molecular biomarkers in lung cancer. Several molecular alterations involving different genes (EGFR, KRAS, ALK, BRAF, and HER2) seem to have a remarkable predilection for adenocarcinoma and specific inhibitors of EGFR and ALK are now available for patients with adenocarcinoma harboring the relevant gene alterations. The efficacy of histology-based and molecular-targeted therapies had a deep impact in (1) re-defining classification of lung cancer (particularly adenocarcinomas) and (2) routine clinical practice of pathologists involved in optimization of handling of tissue samples in order to guarantee NSCLC subtyping with the help of immunohistochemistry and adequately preserve tumor cells for molecular analysis. In agreement with the modern multidisciplinary approach to lung cancer, we reviewed here the diagnostic and predictive value of molecular biomarkers according to the clinical, pathologic, and molecular biologist viewpoints.
© 2013 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  ALK; BRAF; EGFR; HER2; Immunohistochemistry; KRAS; Lung; NSCLC; ROS1; anaplastic lymphoma receptor tyrosine kinase; c-ros oncogene 1, receptor tyrosine kinase; epidermal growth factor receptor; v-Ki-ras2 Kirsten rat sarcoma viral oncogene homolog; v-erb-b2 erythroblastic leukemia viral oncogene homolog 2; v-raf murine sarcoma viral oncogene homolog B1

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Year:  2013        PMID: 24342286     DOI: 10.1053/j.semdp.2013.11.007

Source DB:  PubMed          Journal:  Semin Diagn Pathol        ISSN: 0740-2570            Impact factor:   3.464


  4 in total

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4.  Expression and functional characterization of FOXM1 in non-small cell lung cancer.

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  4 in total

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