Literature DB >> 12430926

Real-time PCR for monitoring minimal residual disease and chimerism in patients after allogeneic transplantation.

Ahmet H Elmaagacli1.   

Abstract

Real-time PCR is a new fluorometric method for cycle-to-cycle quantification of PCR product growth rates. The real-time PCR method is fast and associated with a high reproducibility rate. It is used more often for monitoring MRD and chimerism in patients after allogeneic stem cell transplantation (SCT). There are real-time PCR methods for patients with CML, AML and ALL patients with inv(16), t(8;21), t(15;17); t(1;19) and other chromosomal aberrations. For patients with AML monitoring MRD is useful to identify patients who were at high risk for relapse after receiving chemotherapy. In patients with CML monitoring MRD might be helpful to assess success of after allogeneic SCT, or response to therapies with interferon alfa or STI 571. We found, that it is possible to estimate the relapse stage in CML after SCT by the amount of bcr-abl fusion transcript detected using a real-time PCR method. The median measured bcr-abl amount differ significantly (P<0.001) between the various stages, which has relevant clinical implications because it enables early therapeutic decisions in relapsing patients after transplant as e.g. the application of DLI to induce graft-versus-leukemia effects. Using real-time PCR it is possible to detect differences at alleles between recipient and donor at a single nucleotide basis (SNP) for chimerism analysis. The real-time PCR method enables to achieve a high a sensitivity of up to 1x10(-4), which is much more sensitive than all other chimerism methods including VNTR-PCR, STR-PCR. Furthermore, chimerism in male recipients with a female donor can be monitored also by detecting y-chromosome specific sequences by real-time PCR after transplant, which might be the most sensitive method to detect host type gene sequences. All in all, new real-time PCR methods offer a fast, reliable and very sensitive method to evaluate MRD and chimerism in patients after allogeneic SCT and therefore, to help to identify patients who are at high risk for leukemic relapse.

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Year:  2002        PMID: 12430926     DOI: 10.1007/bf03165118

Source DB:  PubMed          Journal:  Int J Hematol        ISSN: 0925-5710            Impact factor:   2.490


  7 in total

1.  Pre-clinical validation of a novel, highly sensitive assay to detect PML-RARalpha mRNA using real-time reverse-transcription polymerase chain reaction.

Authors:  J L Slack; W Bi; K J Livak; N Beaubier; M Yu; M Clark; S H Kim; R E Gallagher; C L Willman
Journal:  J Mol Diagn       Date:  2001-11       Impact factor: 5.568

2.  Estimating the relapse stage in chronic myeloid leukaemia patients after allogeneic stem cell transplantation by the amount of BCR-ABL fusion transcripts detected using a new real-time polymerase chain reaction method.

Authors:  A H Elmaagacli; A Freist; M Hahn; B Opalka; S Seeber; U W Schaefer; D W Beelen
Journal:  Br J Haematol       Date:  2001-06       Impact factor: 6.998

3.  Real-time reverse transcription polymerase chain reaction detection and quantification of t(1;19) (E2A-PBX1) fusion genes associated with leukaemia.

Authors:  J D Curry; M C Glaser; M T Smith
Journal:  Br J Haematol       Date:  2001-12       Impact factor: 6.998

4.  The TEL-AML1 real-time quantitative polymerase chain reaction (PCR) might replace the antigen receptor-based genomic PCR in clinical minimal residual disease studies in children with acute lymphoblastic leukaemia.

Authors:  V de Haas; W B Breunis; R Dee; O J H M Verhagen; W Kroes; E R van Wering; J J M van Dongen; H van den Berg; C E van der Schoot
Journal:  Br J Haematol       Date:  2002-01       Impact factor: 6.998

5.  The AML1/MTG8 Fusion Transcript in t(8;21) Positive AML and its Implication for the Detection of Minimal Residual Disease; Malignancy.

Authors:  JÜrgen Krauter; Gerhard Heil; Arnold Ganser
Journal:  Hematology       Date:  2001       Impact factor: 2.269

6.  Real-time quantitation of minimal residual disease in inv(16)-positive acute myeloid leukemia may indicate risk for clinical relapse and may identify patients in a curable state.

Authors:  Silvia Buonamici; Emanuela Ottaviani; Nicoletta Testoni; Vittorio Montefusco; Giuseppe Visani; Francesca Bonifazi; Marilina Amabile; Carolina Terragna; Deborah Ruggeri; Pier Paolo Piccaluga; Alessandro Isidori; Michele Malagola; Michele Baccarani; Sante Tura; Giovanni Martinelli
Journal:  Blood       Date:  2002-01-15       Impact factor: 22.113

7.  Kinetics of BCR-ABL fusion transcript levels in chronic myeloid leukemia patients treated with STI571 measured by quantitative real-time polymerase chain reaction.

Authors:  J Stentoft; N Pallisgaard; E Kjeldsen; M S Holm; J L Nielsen; P Hokland
Journal:  Eur J Haematol       Date:  2001 Nov-Dec       Impact factor: 2.997

  7 in total
  3 in total

1.  Feasibility of a cost-effective approach to evaluate short tandem repeat markers suitable for chimerism follow-up.

Authors:  Ariela F Fundia; Carlos De Brasi; Irene Larripa
Journal:  Mol Diagn       Date:  2004

2.  Validation of chimerism in pediatric recipients of allogeneic hematopoietic stem cell transplantation (HSCT) a comparison between two methods: real-time PCR (qPCR) vs. variable number tandem repeats PCR (VNTR PCR).

Authors:  Morris Kletzel; Wei Huang; Marie Olszewski; Sana Khan
Journal:  Chimerism       Date:  2012-12-13

3.  Donor Chimerism Study by Single Nucleotide Polymorphism using SYBR green based Real Time PCR.

Authors:  Ayesha Nayyar; Suhaib Ahmed
Journal:  Pak J Med Sci       Date:  2021 Nov-Dec       Impact factor: 1.088

  3 in total

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