Literature DB >> 20130436

Biological prognostic and predictive factors in lung cancer.

Antonio Rossi1, Domenico Galetta, Cesare Gridelli.   

Abstract

The inclusion of new drugs in clinical research and practice has allowed improvements in several outcomes of advanced non-small-cell lung cancer (NSCLC). Among these drugs, very interesting results have been obtained from pemetrexed and new targeted agents, including the inhibitors of epidermal growth factor receptor (EGFR) such as gefitinib, erlotinib and cetuximab. Unfortunately, these new drugs when investigated for the treatment of small-cell lung cancer (SCLC) reported negative results. The results of these investigations seem to be related to specific factors that could indicate which patients could benefit from each specific therapy. Therefore, several clinical and biological factors might find use as prognostic or predictive markers. A prognostic factor provides information on outcome, independent of the therapy that is used. In contrast, a predictive factor provides information on outcome with regard to a specific therapy. Some factors, such as EGFR mutations, are both prognostic and predictive. In the present paper, we review data related to thymidylate synthase, EGFR and K-ras mutations, the most important biologic prognostic and/or predictive factors related to pemetrexed, gefitinib, erlotinib and cetuximab therapy in the treatment of advanced NSCLC and in SCLC patients. Copyright 2010 S. Karger AG, Basel.

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Year:  2010        PMID: 20130436     DOI: 10.1159/000258500

Source DB:  PubMed          Journal:  Oncology        ISSN: 0030-2414            Impact factor:   2.935


  6 in total

Review 1.  Evaluation of molecular prognostic and predictive factors: an important step towards personalised treatment in non small cell lung cancer.

Authors:  Alfredo Tartarone; Rose Lerose; Giuseppina Gallucci; Raffaele Ardito; Michele Aieta
Journal:  Med Oncol       Date:  2011-06-02       Impact factor: 3.064

2.  Proteomic markers of DNA repair and PI3K pathway activation predict response to the PARP inhibitor BMN 673 in small cell lung cancer.

Authors:  Robert J Cardnell; Ying Feng; Lixia Diao; You-Hong Fan; Fatemah Masrorpour; Jing Wang; Yuqiao Shen; Gordon B Mills; John D Minna; John V Heymach; Lauren A Byers
Journal:  Clin Cancer Res       Date:  2013-09-27       Impact factor: 12.531

3.  Molecular testing guideline for selection of lung cancer patients for EGFR and ALK tyrosine kinase inhibitors: guideline from the College of American Pathologists, International Association for the Study of Lung Cancer, and Association for Molecular Pathology.

Authors:  Neal I Lindeman; Philip T Cagle; Mary Beth Beasley; Dhananjay Arun Chitale; Sanja Dacic; Giuseppe Giaccone; Robert Brian Jenkins; David J Kwiatkowski; Juan-Sebastian Saldivar; Jeremy Squire; Erik Thunnissen; Marc Ladanyi
Journal:  J Thorac Oncol       Date:  2013-07       Impact factor: 15.609

4.  Molecular testing guideline for selection of lung cancer patients for EGFR and ALK tyrosine kinase inhibitors: guideline from the College of American Pathologists, International Association for the Study of Lung Cancer, and Association for Molecular Pathology.

Authors:  Neal I Lindeman; Philip T Cagle; Mary Beth Beasley; Dhananjay Arun Chitale; Sanja Dacic; Giuseppe Giaccone; Robert Brian Jenkins; David J Kwiatkowski; Juan-Sebastian Saldivar; Jeremy Squire; Erik Thunnissen; Marc Ladanyi
Journal:  Arch Pathol Lab Med       Date:  2013-04-03       Impact factor: 5.534

5.  Permissiveness of human cancer cells to oncolytic bovine herpesvirus 1 is mediated in part by KRAS activity.

Authors:  Breanne P Cuddington; Karen L Mossman
Journal:  J Virol       Date:  2014-04-02       Impact factor: 5.103

6.  Mutated KRAS Is an Independent Negative Prognostic Factor for Survival in NSCLC Stage III Disease Treated with High-Dose Radiotherapy.

Authors:  A Hallqvist; F Enlund; C Andersson; H Sjögren; A Hussein; E Holmberg; J Nyman
Journal:  Lung Cancer Int       Date:  2012-09-17
  6 in total

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