Literature DB >> 7578520

Kinetics of minimal residual disease during induction/consolidation therapy in standard-risk adult B-lineage acute lymphoblastic leukemia.

C Scholten1, M Födinger, M Mitterbauer, K Laczika, G Mitterbauer, O A Haas, P Knöbl, I Schwarzinger, R Thalhammer, B Purtscher.   

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 receptor gamma chain gene (TCR gamma), 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 10(2-3) for the CDR3- and TCR gamma-PCR and one in 10(5-6) for a two-step, seminested CDR3/clone-specific PCR. At diagnosis, 7/7 patients were CDR3 positive and four were TCR gamma positive in their bone marrow (BM). At the end of induction therapy (after 2 months) 4/6 tested positive for CDR3, 2/6 for TCR gamma, 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 TCR gamma, 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.

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Year:  1995        PMID: 7578520     DOI: 10.1007/BF01910311

Source DB:  PubMed          Journal:  Ann Hematol        ISSN: 0939-5555            Impact factor:   3.673


  31 in total

Review 1.  The biology and treatment of acute lymphoblastic leukemia in adults.

Authors:  E A Copelan; E A McGuire
Journal:  Blood       Date:  1995-03-01       Impact factor: 22.113

2.  Minimal residual disease in childhood B-lineage lymphoblastic leukemia. Persistence of leukemic cells during the first 18 months of treatment.

Authors:  M Yamada; R Wasserman; B Lange; B A Reichard; R B Womer; G Rovera
Journal:  N Engl J Med       Date:  1990-08-16       Impact factor: 91.245

3.  Residual disease detection in multiple follow-up samples in children with acute lymphoblastic leukemia.

Authors:  G R Kitchingman
Journal:  Leukemia       Date:  1994-03       Impact factor: 11.528

4.  High efficacy of the German multicenter ALL (GMALL) protocol for treatment of adult acute lymphoblastic leukemia (ALL)--a single-institution study.

Authors:  R Scherrer; P Bettelheim; K Geissler; U Jäger; P Knöbl; P A Kyrle; K Laczika; G Mitterbauer; E Neumann; B Schneider
Journal:  Ann Hematol       Date:  1994-10       Impact factor: 3.673

5.  Detection of minimal residual disease in T-cell acute lymphoblastic leukemia using polymerase chain reaction predicts impending relapse.

Authors:  G A Neale; J Menarguez; G R Kitchingman; T J Fitzgerald; M Koehler; J Mirro; R M Goorha
Journal:  Blood       Date:  1991-08-01       Impact factor: 22.113

6.  Molecular residual disease status at the end of chemotherapy fails to predict subsequent relapse in children with B-lineage acute lymphoblastic leukemia.

Authors:  Y Ito; R Wasserman; N Galili; B A Reichard; S Shane; B Lange; G Rovera
Journal:  J Clin Oncol       Date:  1993-03       Impact factor: 44.544

7.  Prospective monitoring and quantitation of residual blasts in childhood acute lymphoblastic leukemia by polymerase chain reaction study of delta and gamma T-cell receptor genes.

Authors:  H Cavé; C Guidal; P Rohrlich; M H Delfau; A Broyart; B Lescoeur; C Rahimy; O Fenneteau; N Monplaisir; L d'Auriol
Journal:  Blood       Date:  1994-04-01       Impact factor: 22.113

8.  Minimal residual disease in childhood acute lymphoblastic leukemia: analysis of patients in continuous complete remission or with consecutive relapse.

Authors:  A Biondi; S Yokota; T E Hansen-Hagge; V Rossi; G Giudici; O Maglia; G Basso; C Tell; G Masera; C R Bartram
Journal:  Leukemia       Date:  1992-04       Impact factor: 11.528

9.  Detection of minimal residual disease using clonospecific primers for CDRIII in patients with acute B lymphocytic leukemia with or without Philadelphia chromosome: possibility of clinical application as a tool for improving prognosis.

Authors:  Y Maeda; F Horiuchi; S Morita; M Matsuda; C Shirakawa; H Masaki; A Koyama; H Hamazaki; T Fujimoto; K Irimajiri
Journal:  Exp Hematol       Date:  1994-08       Impact factor: 3.084

10.  Outcome prediction in childhood acute lymphoblastic leukaemia by molecular quantification of residual disease at the end of induction.

Authors:  M J Brisco; J Condon; E Hughes; S H Neoh; P J Sykes; R Seshadri; I Toogood; K Waters; G Tauro; H Ekert
Journal:  Lancet       Date:  1994-01-22       Impact factor: 79.321

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  1 in total

Review 1.  Detection of minimal residual disease in multiple myeloma and acute leukaemia.

Authors:  M H Bakkus; N Juge-Morineau; J E van der Werff ten Bosch
Journal:  Med Oncol       Date:  1996-06       Impact factor: 3.064

  1 in total

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