RAWSTRON, A.C., C. FAZI, A. AGATHANGELIDIS, N. VILLAMOR, R. LETESTU, J. NOMDEDEU, C. PALACIO, Olga STEHLÍKOVÁ, K-A. KREUZER, S. LIPTROT, D. O´BRIEN, R.M. DE TUTE, I. MARINOV, M. HAUWEL, M. SPACEK, J. DOBBER, A.P. KATER, P. GAMBELL, A. SOOSAPILLA, G. LOZANSKI, G. BRACHTL, K. LIN, J. BOYSEN, C. HANSON, J.L. JORGENSEN, M. STETLER-STEVENSON, C. YUAN, H.E. BROOME, L. RASSENTI, F. CRAIG, J. DELGADO, C. MORENO, F. BOSCH, A. EGLE, Michael DOUBEK, Šárka POSPÍŠILOVÁ, S. MULLIGAN, D. WESTERMAN, C.M. SANDERS, R. EMERSON, H.S. ROBINS, I. KIRSCH, T. SHANAFELT, A. PETTITT, T.J. KIPPS, W.G. WIERDA, F. CYMBALISTA, M. HALLEK, P. HILLMEN, E. MONTSERRAT and P. GHIA. A complementary role of multiparameter flow cytometry and high-throughput sequencing for minimal residual disease detection in chronic lymphocytic leukemia: an European Research Initiative on CLL study. Leukemia. London: Nature Publishing Group, 2016, vol. 30, No 4, p. 929-936. ISSN 0887-6924. Available from: https://dx.doi.org/10.1038/leu.2015.313. |
Other formats:
BibTeX
LaTeX
RIS
@article{1354166, author = {Rawstron, A.C. and Fazi, C. and Agathangelidis, A. and Villamor, N. and Letestu, R. and Nomdedeu, J. and Palacio, C. and Stehlíková, Olga and Kreuzer, KandA. and Liptrot, S. and O´Brien, D. and de Tute, R.M. and Marinov, I. and Hauwel, M. and Spacek, M. and Dobber, J. and Kater, A.P. and Gambell, P. and Soosapilla, A. and Lozanski, G. and Brachtl, G. and Lin, K. and Boysen, J. and Hanson, C. and Jorgensen, J.L. and StetlerandStevenson, M. and Yuan, C. and Broome, H.E. and Rassenti, L. and Craig, F. and Delgado, J. and Moreno, C. and Bosch, F. and Egle, A. and Doubek, Michael and Pospíšilová, Šárka and Mulligan, S. and Westerman, D. and Sanders, C.M. and Emerson, R. and Robins, H.S. and Kirsch, I. and Shanafelt, T. and Pettitt, A. and Kipps, T.J. and Wierda, W.G. and Cymbalista, F. and Hallek, M. and Hillmen, P. and Montserrat, E. and Ghia, P.}, article_location = {London}, article_number = {4}, doi = {http://dx.doi.org/10.1038/leu.2015.313}, keywords = {ASSAY; QUANTIFICATION; RITUXIMAB; SURVIVAL; THERAPY; ERADICATION; EXPRESSION; GUIDELINES; DIAGNOSIS; TRIAL}, language = {eng}, issn = {0887-6924}, journal = {Leukemia}, title = {A complementary role of multiparameter flow cytometry and high-throughput sequencing for minimal residual disease detection in chronic lymphocytic leukemia: an European Research Initiative on CLL study}, url = {https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4832072/pdf/leu2015313a.pdf}, volume = {30}, year = {2016} }
TY - JOUR ID - 1354166 AU - Rawstron, A.C. - Fazi, C. - Agathangelidis, A. - Villamor, N. - Letestu, R. - Nomdedeu, J. - Palacio, C. - Stehlíková, Olga - Kreuzer, K-A. - Liptrot, S. - O´Brien, D. - de Tute, R.M. - Marinov, I. - Hauwel, M. - Spacek, M. - Dobber, J. - Kater, A.P. - Gambell, P. - Soosapilla, A. - Lozanski, G. - Brachtl, G. - Lin, K. - Boysen, J. - Hanson, C. - Jorgensen, J.L. - Stetler-Stevenson, M. - Yuan, C. - Broome, H.E. - Rassenti, L. - Craig, F. - Delgado, J. - Moreno, C. - Bosch, F. - Egle, A. - Doubek, Michael - Pospíšilová, Šárka - Mulligan, S. - Westerman, D. - Sanders, C.M. - Emerson, R. - Robins, H.S. - Kirsch, I. - Shanafelt, T. - Pettitt, A. - Kipps, T.J. - Wierda, W.G. - Cymbalista, F. - Hallek, M. - Hillmen, P. - Montserrat, E. - Ghia, P. PY - 2016 TI - A complementary role of multiparameter flow cytometry and high-throughput sequencing for minimal residual disease detection in chronic lymphocytic leukemia: an European Research Initiative on CLL study JF - Leukemia VL - 30 IS - 4 SP - 929-936 EP - 929-936 PB - Nature Publishing Group SN - 08876924 KW - ASSAY KW - QUANTIFICATION KW - RITUXIMAB KW - SURVIVAL KW - THERAPY KW - ERADICATION KW - EXPRESSION KW - GUIDELINES KW - DIAGNOSIS KW - TRIAL UR - https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4832072/pdf/leu2015313a.pdf L2 - https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4832072/pdf/leu2015313a.pdf N2 - In chronic lymphocytic leukemia (CLL) the level of minimal residual disease (MRD) after therapy is an independent predictor of outcome. Given the increasing number of new agents being explored for CLL therapy, using MRD as a surrogate could greatly reduce the time necessary to assess their efficacy. In this European Research Initiative on CLL (ERIC) project we have identified and validated a flow-cytometric approach to reliably quantitate CLL cells to the level of 0.0010% (10(-5)). The assay comprises a core panel of six markers (i.e. CD19, CD20, CD5, CD43, CD79b and CD81) with a component specification independent of instrument and reagents, which can be locally re-validated using normal peripheral blood. This method is directly comparable to previous ERIC-designed assays and also provides a backbone for investigation of new markers. A parallel analysis of high-throughput sequencing using the ClonoSEQ assay showed good concordance with flow cytometry results at the 0.010% (10(-4)) level, the MRD threshold defined in the 2008 International Workshop on CLL guidelines, but it also provides good linearity to a detection limit of 1 in a million (10(-6)). The combination of both technologies would permit a highly sensitive approach to MRD detection while providing a reproducible and broadly accessible method to quantify residual disease and optimize treatment in CLL. ER -
RAWSTRON, A.C., C. FAZI, A. AGATHANGELIDIS, N. VILLAMOR, R. LETESTU, J. NOMDEDEU, C. PALACIO, Olga STEHLÍKOVÁ, K-A. KREUZER, S. LIPTROT, D. O´BRIEN, R.M. DE TUTE, I. MARINOV, M. HAUWEL, M. SPACEK, J. DOBBER, A.P. KATER, P. GAMBELL, A. SOOSAPILLA, G. LOZANSKI, G. BRACHTL, K. LIN, J. BOYSEN, C. HANSON, J.L. JORGENSEN, M. STETLER-STEVENSON, C. YUAN, H.E. BROOME, L. RASSENTI, F. CRAIG, J. DELGADO, C. MORENO, F. BOSCH, A. EGLE, Michael DOUBEK, Šárka POSPÍŠILOVÁ, S. MULLIGAN, D. WESTERMAN, C.M. SANDERS, R. EMERSON, H.S. ROBINS, I. KIRSCH, T. SHANAFELT, A. PETTITT, T.J. KIPPS, W.G. WIERDA, F. CYMBALISTA, M. HALLEK, P. HILLMEN, E. MONTSERRAT and P. GHIA. A complementary role of multiparameter flow cytometry and high-throughput sequencing for minimal residual disease detection in chronic lymphocytic leukemia: an European Research Initiative on CLL study. \textit{Leukemia}. London: Nature Publishing Group, 2016, vol.~30, No~4, p.~929-936. ISSN~0887-6924. Available from: https://dx.doi.org/10.1038/leu.2015.313.
|