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Kinetics of minimal residual disease during induction/consolidation therapy in standard-risk adult B-lineage acute lymphoblastic leukemia
Authors:C. Scholten  M. Födinger  M. Mitterbauer  K. Laczika  G. Mitterbauer  O. A. Haas  P. Knöbl  I. Schwarzinger  R. Thalhammer  B. Purtscher  K. Geissler  C. Mannhalter  K. Lechner  U. Jaeger
Affiliation:(1) Department of Internal Medicine I, Division of Hematology and Hemostaseology, Währinger Gürtel 18–20, A-1090 Vienna, Austria;(2) Department of Clinical Chemistry and Laboratory Diagnostics, University of Vienna, Austria;(3) CCRI, St. Anna Children's Hospital, University of Vienna, Austria
Abstract:We have compared the kinetics of minimal residual disease (MRD) by simultaneous polymerase chain reaction (PCR) monitoring with oligonucleotides for the immunoglobulin heavy chain (IgH) complementarity-determining region 3 (CDR3) and the T-cell receptorgamma chain gene (TCRgamma), as well as clone-specific CDR3 sequences in adult patients (aged 17–51 years) with acute lymphoblastic leukemia (ALL) who entered a complete hematological remission (CR) after chemotherapy with the German multicenter ALL (GMALL) protocol. The sensitivities were one in 102–3 for the CDR3- and TCRgamma-PCR and one in 105–6 for a two-step, seminested CDR3/clone-specific PCR. At diagnosis, 7/7 patients were CDR3 positive and four were TCRgamma positive in their bone marrow (BM). At the end of induction therapy (after 2 months) 4/6 tested positive for CDR3, 2/6 for TCRgamma, and 5/6 for clone-specific rearrangements. At the end of consolidation treatment (after 7 months) only 1/7 remained positive for CDR3, 2/7 for TCRgamma, and 5/7 for clone-specific rearrangements. After an observation period of 18–36 months, 4/7 patients were still in CR and all were PCR negative by the clone-specific method during or after maintenance therapy. Two patients died in leukemic relapse; one patient relapsed but is still alive. All three of these patients remained PCR positive throughout the course of their disease. Clonal evolution in the IgH locus was found in one of these patients. We conclude that the molecular response to chemotherapy in adult B-lineage ALL is slow, even in patients without risk factors other than age. As in childhood ALL, most patients with long-term CR convert to PCR negativity approximately 18 months after the start of chemotherapy. The data also suggest the existence of early clone-specific PCR negativity in a small proportion of long-term survivors. The predictive value of this observation will now have to be confirmed in a larger study.
Keywords:CDR3-PCR  Clone-specific PCR  TCR  /content/j2689941228r69qj/xxlarge947.gif"   alt="  gamma"   align="  MIDDLE"   BORDER="  0"  >-PCR  Adult B-lineage ALL
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