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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.
CLINICAL TRIALS AND OBSERVATIONS CD10- pre-B acute lymphoblastic leukemia (ALL) is 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)From the Department of Internal Medicine III, Campus Benjamin Franklin, Charité Universitätsmedizin, Berlin, Germany; Department of Hematology, Goethe University, Frankfurt, Germany; Institute of Human Genetics and Anthropology, Heinrich-Heine Universität, Düsseldorf, Germany; Department of Hematology and Oncology, Campus Virchow, Charité Universitätsmedizin, Berlin, Germany; Department of Hematology and Oncology, Medical University of Hannover, Germany; Laboratory for Leukemia-Diagnostics, Department of Internal Medicine III, University Hospital Großhadern, Munich, Germany; Laboratory for Tumor Cytogenetics, University of Ulm, Germany; Department of Human Genetics, KIMCL, Medical Institute for Medical Biology, University of Vienna, Austria; and Institute of Human Genetics, University of Heidelberg, Germany.
Immunophenotyping disclosed CD10 negativity in 70 of 2408 cases of B-lineage acute lymphoblastic leukemia (ALL), although other criteria followed classification of pre-B ALL (eg, 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 or an 11q23/MLL rearrangement or both were evident in 46 of 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- 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- pre-B ALL. Our data identify CD10- cytoplasmic immunoglobulin-positive pre-B ALL as a rare (2.2%) but distinct immuno-subtype of adult ALL that is characterized by a high MLL rearrangement rate and a worse outcome.
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