Detection of Crizotinib-Sensitive Lung Adenocarcinomas With MET, ALK, and ROS1 Genomic Alterations via Comprehensive Genomic Profiling.

PubWeight™: 0.80‹?›

🔗 View Article (PMID 25922291)

Published in Clin Lung Cancer on March 25, 2015

Authors

Xiuning Le1, Jason A Freed1, Paul A VanderLaan2, Mark S Huberman1, Deepa Rangachari1, Susan E Jorge1, Antonio R Lucena-Araujo1, Susumu S Kobayashi1, Sohail Balasubramanian3, Jie He3, Yakov Chudnovsky3, Vincent A Miller3, Siraj M Ali3, Daniel B Costa4

Author Affiliations

1: Department of Medicine, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA.
2: Department of Pathology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA.
3: Foundation Medicine, Inc, Cambridge, MA.
4: Department of Medicine, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA. Electronic address: dbcosta@bidmc.harvard.edu.

Associated clinical trials:

A Study Of Oral PF-02341066, A C-Met/Hepatocyte Growth Factor Tyrosine Kinase Inhibitor, In Patients With Advanced Cancer (PROFILE 1001) | NCT00585195

Articles cited by this

Cancer statistics, 2014. CA Cancer J Clin (2014) 72.81

Anaplastic lymphoma kinase inhibition in non-small-cell lung cancer. N Engl J Med (2010) 36.78

Crizotinib versus chemotherapy in advanced ALK-positive lung cancer. N Engl J Med (2013) 14.78

Development and validation of a clinical cancer genomic profiling test based on massively parallel DNA sequencing. Nat Biotechnol (2013) 7.97

Cytoreductive antitumor activity of PF-2341066, a novel inhibitor of anaplastic lymphoma kinase and c-Met, in experimental models of anaplastic large-cell lymphoma. Mol Cancer Ther (2007) 7.08

Crizotinib in ROS1-rearranged non-small-cell lung cancer. N Engl J Med (2014) 6.95

Using multiplexed assays of oncogenic drivers in lung cancers to select targeted drugs. JAMA (2014) 6.32

An orally available small-molecule inhibitor of c-Met, PF-2341066, exhibits cytoreductive antitumor efficacy through antiproliferative and antiangiogenic mechanisms. Cancer Res (2007) 5.63

Amplification of MET may identify a subset of cancers with extreme sensitivity to the selective tyrosine kinase inhibitor PHA-665752. Proc Natl Acad Sci U S A (2006) 5.23

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. J Thorac Oncol (2013) 3.71

Cell line-based platforms to evaluate the therapeutic efficacy of candidate anticancer agents. Nat Rev Cancer (2010) 3.33

Management and future directions in non-small cell lung cancer with known activating mutations. Am Soc Clin Oncol Educ Book (2014) 1.68

Preclinical rationale for use of the clinically available multitargeted tyrosine kinase inhibitor crizotinib in ROS1-translocated lung cancer. J Thorac Oncol (2012) 1.66

Epidermal growth factor receptor (EGFR) mutations in lung cancer: preclinical and clinical data. Braz J Med Biol Res (2014) 1.16