TY - JOUR
T1 - Identification of a 3-gene model as a powerful diagnostic tool for the recognition of ALK-negative anaplastic large-cell lymphoma
AU - Agnelli, Luca
AU - Mereu, Elisabetta
AU - Pellegrino, Elisa
AU - Limongi, Tania
AU - Kwee, Ivo
AU - Bergaggio, Elisa
AU - Ponzoni, Maurilio
AU - Zamò, Alberto
AU - Iqbal, Javeed
AU - Piccaluga, Pier Paolo
AU - Neri, Antonino
AU - Chan, Wing C.
AU - Pileri, Stefano
AU - Bertoni, Francesco
AU - Inghirami, Giorgio
AU - Piva, Roberto
PY - 2012/8/9
Y1 - 2012/8/9
N2 - Anaplastic large-cell lymphomas (ALCLs) are a group of clinically and biologically heterogeneous diseases including the ALK+ and ALK+ systemic forms. Whereas ALK+ ALCLs are molecularly characterized and can be readily diagnosed, specific immunophenotypic or genetic features to define ALK- ALCL are missing, and their distinction from other T-cell non-Hodgkin lymphomas (T-NHLs) remains controversial. In the present study, we undertook a transcriptional profiling meta-analysis of 309 cases, including ALCL and other primary T-NHL samples. Pathway discovery and prediction analyses defined a minimum set of genes capable of recognizing ALK- ALCL. Application of quantitative RT-PCR in independent datasets from cryopreserved and formalin-fixed paraffin-embedded samples validated a 3-gene model (TNFRSF8, BATF3, and TMOD1) able to successfully separate ALK- ALCL from peripheral T-cell lymphoma not otherwise specified, with overall accuracy near 97%. In conclusion, our data justify the possibility of translating quantitative RT-PCR protocols to routine clinical settings as a new approach to objectively dissect T-NHL and to select more appropriate therapeutic protocols.
AB - Anaplastic large-cell lymphomas (ALCLs) are a group of clinically and biologically heterogeneous diseases including the ALK+ and ALK+ systemic forms. Whereas ALK+ ALCLs are molecularly characterized and can be readily diagnosed, specific immunophenotypic or genetic features to define ALK- ALCL are missing, and their distinction from other T-cell non-Hodgkin lymphomas (T-NHLs) remains controversial. In the present study, we undertook a transcriptional profiling meta-analysis of 309 cases, including ALCL and other primary T-NHL samples. Pathway discovery and prediction analyses defined a minimum set of genes capable of recognizing ALK- ALCL. Application of quantitative RT-PCR in independent datasets from cryopreserved and formalin-fixed paraffin-embedded samples validated a 3-gene model (TNFRSF8, BATF3, and TMOD1) able to successfully separate ALK- ALCL from peripheral T-cell lymphoma not otherwise specified, with overall accuracy near 97%. In conclusion, our data justify the possibility of translating quantitative RT-PCR protocols to routine clinical settings as a new approach to objectively dissect T-NHL and to select more appropriate therapeutic protocols.
UR - http://www.scopus.com/inward/record.url?scp=84865176067&partnerID=8YFLogxK
U2 - 10.1182/blood-2012-01-405555
DO - 10.1182/blood-2012-01-405555
M3 - Article
C2 - 22740451
AN - SCOPUS:84865176067
SN - 0006-4971
VL - 120
SP - 1274
EP - 1281
JO - Blood
JF - Blood
IS - 6
ER -