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Blood, 15 December 2005, Vol. 106, No. 13, pp. 4054-4056.
Prepublished online as a Blood First Edition Paper on August 25, 2005; DOI 10.1182/blood-2005-05-1866.


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Submitted May 10, 2005
Accepted August 11, 2005

CD10-negative pre-B acute lymphoblastic leukemia (ALL): a distinct high-risk subgroup of adult ALL associated with a high frequency of MLL aberrations. Results of the German Multicenter Trials for Adult ALL (GMALL)

Beate Gleissner*, Nicola Goekbuget, Harald Rieder, Renate Arnold, Stefan Schwartz, Helmut Diedrich, Claudia Schoch, Barbara Heinze, Christa Fonatsch, Claus R Bartram, Dieter Hoelzer, and Eckhard Thiel

Internal Medicine III, Charite Universitaetsmedizin, Campus Benjamin Franklin, Berlin, Germany
Department of Hematology, Goethe University, Frankfurt, Germany
Institute of Human Genetics and Anthropology, Heinrich-Heine University, Duesseldorf, Germany
Department of Hematology and Oncology, Charite Universitaetsmedizin, Campus Virchow, Berlin, Germany
Department of Hematology and Oncology, Medical University, Hannover, Germany
Department of Internal Medicine III, Laboratory for Leukemia-Diagnostics, University Hospital Grosshadern, Muenchen, Germany
Laboratory for Tumor Cytogenetics, University of Ulm, Ulm, Germany
Department of Human Genetics, KIMCL, Medical Institute for Medical Biology, University of Vienna, Vienna, Austria
Insitute of Human Genetics, University of Heidelberg, Heidelberg, Germany

* Corresponding author; email: beate.gleissner{at}charite.de.

Immunophenotyping disclosed CD10-negativity in 70 of 2,408 cases of B-lineage acute lymphoblastic leukemia (ALL), although other criteria followed classification of pre-B ALL (e.g., cytoplasmic immunoglobulin positivity). These blasts showed high myeloid antigen expression (60% CD65-positivity) and reacted with antibody 7.1 in 95% of the cases. MLL-AF4 fusion transcripts and/or an 11q23/MLL rearrangement were evident in 46/56 samples (82%). Although 83% of the patients achieved complete remission, the remission duration remained remarkably low: 141 days for MLL-rearrangement-positive and 245 days for MLL-rearrangement-negative CD10-negative pre-B ALL. Thus the overall survival probability 3 years after diagnosis was 0.34 (± 0.20 SE) in MLL-rearrangement-negative versus 0.12 (± 0.06 SE) in MLL-rearrangement-positive CD10-negative pre-B ALL. Our data identify CD10-negative cytoplasmic Ig-positive pre-B ALL as a rare (2.2%) but distinct immunosubtype of adult ALL that is characterized by a high MLL rearrangement rate and a worse outcome.


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