TY - JOUR
T1 - The role of molecular analyses in the era of personalized therapy for advanced NSCLC
AU - Tanner, Nichole T.
AU - Pastis, Nicholas J.
AU - Sherman, Carol
AU - Simon, George R.
AU - Lewin, David
AU - Silvestri, Gerard A.
N1 - Funding Information:
Financial support for medical and editorial assistance was provided by Boehringer Ingelheim Pharmaceuticals. The authors received no compensation related to the development of the manuscript. Writing and editorial assistance was provided by Lisa Shannon, PharmD of MedErgy, which was contracted by Boehringer Ingelheim Pharmaceuticals for these services. The authors meet criteria for authorship as recommended by the International Committee of Medical Journal Editors (ICMJE), were fully responsible for all content and editorial decisions, and were involved at all stages of manuscript development.
PY - 2012/5
Y1 - 2012/5
N2 - Platinum-based doublet chemotherapy is the traditional treatment of choice for advanced non-small cell lung cancer (NSCLC); however, the efficacy of these regimens has reached a plateau. Increasing evidence demonstrates that patients with sensitizing mutations in the . epidermal growth factor receptor (. EGFR) experience improved progression-free survival and response rates with first-line gefitinib or erlotinib therapy relative to traditional platinum-based chemotherapy, while patients with . EGFR-mutation negative tumors gain greater benefit from platinum-based chemotherapy. These results highlight the importance of molecular testing prior to the initiation of first-line therapy for advanced NSCLC. Routine molecular testing of tumor samples represents an important paradigm shift in NSCLC therapy and would allow for individualized therapy in specific subsets of patients. As these and other advances in personalized treatment are integrated into everyday clinical practice, pulmonologists will play a vital role in ensuring that tumor samples of adequate quality and quantity are collected in order to perform appropriate molecular analyses to guide treatment decisions. This article provides an overview of clinical trial data supporting molecular analysis of NSCLC, describes specimen acquisition and testing methods currently in use, and discusses future directions of personalized therapy for patients with NSCLC.
AB - Platinum-based doublet chemotherapy is the traditional treatment of choice for advanced non-small cell lung cancer (NSCLC); however, the efficacy of these regimens has reached a plateau. Increasing evidence demonstrates that patients with sensitizing mutations in the . epidermal growth factor receptor (. EGFR) experience improved progression-free survival and response rates with first-line gefitinib or erlotinib therapy relative to traditional platinum-based chemotherapy, while patients with . EGFR-mutation negative tumors gain greater benefit from platinum-based chemotherapy. These results highlight the importance of molecular testing prior to the initiation of first-line therapy for advanced NSCLC. Routine molecular testing of tumor samples represents an important paradigm shift in NSCLC therapy and would allow for individualized therapy in specific subsets of patients. As these and other advances in personalized treatment are integrated into everyday clinical practice, pulmonologists will play a vital role in ensuring that tumor samples of adequate quality and quantity are collected in order to perform appropriate molecular analyses to guide treatment decisions. This article provides an overview of clinical trial data supporting molecular analysis of NSCLC, describes specimen acquisition and testing methods currently in use, and discusses future directions of personalized therapy for patients with NSCLC.
KW - Epidermal growth factor receptor (EGFR)
KW - Kirsten rat sarcoma viral oncogene homolog (KRAS)
KW - Molecular testing
KW - Non-small cell lung cancer
KW - Personalized medicine
KW - Tyrosine kinase inhibitors
UR - https://www.scopus.com/pages/publications/84859424193
UR - https://www.scopus.com/pages/publications/84859424193#tab=citedBy
U2 - 10.1016/j.lungcan.2011.11.013
DO - 10.1016/j.lungcan.2011.11.013
M3 - Review article
C2 - 22176813
AN - SCOPUS:84859424193
SN - 0169-5002
VL - 76
SP - 131
EP - 137
JO - Lung Cancer
JF - Lung Cancer
IS - 2
ER -