TY - JOUR
T1 - A genomics-based classification of human lung tumors
AU - The Clinical Lung Cancer Genome Project (CLCGP) and Network Genomic Medicine (NGM)
AU - Seidel, Danila
AU - Zander, Thomas
AU - Heukamp, Lukas C.
AU - Peifer, Martin
AU - Bos, Marc
AU - Fernández-Cuesta, Lynnette
AU - Leenders, Frauke
AU - Lu, Xin
AU - Ansén, Sascha
AU - Gardizi, Masyar
AU - Nguyen, Chau
AU - Berg, Johannes
AU - Russell, Prudence
AU - Wainer, Zoe
AU - Schildhaus, Hans Ulrich
AU - Rogers, Toni Maree
AU - Solomon, Benjamin
AU - Pao, William
AU - Carter, Scott L.
AU - Getz, Gad
AU - Hayes, D. Neil
AU - Wilkerson, Matthew D.
AU - Thunnissen, Erik
AU - Travis, William D.
AU - Perner, Sven
AU - Wright, Gavin
AU - Brambilla, Elisabeth
AU - Büttner, Reinhard
AU - Wolf, Jürgen
AU - Thomas, Roman K.
AU - Gabler, Franziska
AU - Wilkening, Ines
AU - Müller, Christian
AU - Dahmen, Ilona
AU - Menon, Roopika
AU - König, Katharina
AU - Albus, Kerstin
AU - Merkelbach-Bruse, Sabine
AU - Fassunke, Jana
AU - Schmitz, Katja
AU - Kuenstlinger, Helen
AU - Kleine, Michaela A.
AU - Binot, Elke
AU - Querings, Silvia
AU - Altmüller, Janine
AU - Bäßmann, Ingelore
AU - Nürnberg, Peter
AU - Schneider, Peter M.
AU - Bogus, Magdalena
AU - Soltermann, Alex
PY - 2013/10/30
Y1 - 2013/10/30
N2 - We characterized genome alterations in 1255 clinically annotated lung tumors of all histological subgroups to identify genetically defined and clinically relevant subtypes. More than 55% of all cases had at least one oncogenic genome alteration potentially amenable to specific therapeutic intervention, including several personalized treatment approaches that are already in clinical evaluation. Marked differences in the patternof genomic alterations existed between and within histological subtypes, thus challenging the original histomorphological diagnosis. Immunohistochemical studies confirmed many of these reassigned subtypes. The reassignment eliminated almost all cases of large cell carcinomas, some of which had therapeutically relevant alterations. Prospective testing of our genomics-based diagnostic algorithm in 5145 lung cancer patients enabled a genome-based diagnosis in 3863 (75%) patients, confirmed the feasibility of rational reassignments of large cell lung cancer, and led to improvement in overall survival in patients with EGFRmutant or ALK-rearranged cancers. Thus, our findings provide support for broad implementation of genomebased diagnosis of lung cancer.
AB - We characterized genome alterations in 1255 clinically annotated lung tumors of all histological subgroups to identify genetically defined and clinically relevant subtypes. More than 55% of all cases had at least one oncogenic genome alteration potentially amenable to specific therapeutic intervention, including several personalized treatment approaches that are already in clinical evaluation. Marked differences in the patternof genomic alterations existed between and within histological subtypes, thus challenging the original histomorphological diagnosis. Immunohistochemical studies confirmed many of these reassigned subtypes. The reassignment eliminated almost all cases of large cell carcinomas, some of which had therapeutically relevant alterations. Prospective testing of our genomics-based diagnostic algorithm in 5145 lung cancer patients enabled a genome-based diagnosis in 3863 (75%) patients, confirmed the feasibility of rational reassignments of large cell lung cancer, and led to improvement in overall survival in patients with EGFRmutant or ALK-rearranged cancers. Thus, our findings provide support for broad implementation of genomebased diagnosis of lung cancer.
UR - http://www.scopus.com/inward/record.url?scp=84890046280&partnerID=8YFLogxK
U2 - 10.1126/scitranslmed.3006802
DO - 10.1126/scitranslmed.3006802
M3 - Article
C2 - 24174329
AN - SCOPUS:84890046280
SN - 1946-6234
VL - 5
JO - Science Translational Medicine
JF - Science Translational Medicine
IS - 209
M1 - 209ra153
ER -