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Allogeneic stem cell transplantation for chronic lymphocytic leukemia: Lessons to be learned from minimal residual disease studies

Allogeneic stem cell transplantation (alloSCT) is a potentially curative treatment strategy for poor-risk chronic lymphocytic leukemia (CLL). The crucial anti-leukemic principle of alloSCT in CLL appears to be the graft-versus-leukemia effect (GVL). Evidence for GVL in CLL is particularly provided b...

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Bibliographic Details
Main Authors: Böttcher, Sebastian (Author) , Ritgen, Matthias (Author) , Dreger, Peter (Author)
Format: Article (Journal)
Language:English
Published: 26 January 2011
In: Blood reviews
Year: 2011, Volume: 25, Issue: 2, Pages: 91-96
ISSN:1532-1681
DOI:10.1016/j.blre.2011.01.001
Online Access:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1016/j.blre.2011.01.001
Verlag, lizenzpflichtig, Volltext: https://www.sciencedirect.com/science/article/pii/S0268960X11000026
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Author Notes:Sebastian Böttcher, Matthias Ritgen, Peter Dreger
Description
Summary:Allogeneic stem cell transplantation (alloSCT) is a potentially curative treatment strategy for poor-risk chronic lymphocytic leukemia (CLL). The crucial anti-leukemic principle of alloSCT in CLL appears to be the graft-versus-leukemia effect (GVL). Evidence for GVL in CLL is particularly provided by studies analysing the kinetics of minimal residual disease (MRD). The purpose of this review is to summarize the methodologies of MRD assessment, its proven benefits and its further perspectives for optimizing the outcome of transplantation. Proven value of quantitative MRD monitoring by RQ-PCR or MRD-flow consists in using it as an indicator of long-term disease control and potential cure. As MRD kinetics correlates with GVL activity, its suitability for guiding GVL-inducing immunomodulation is currently under investigation. In conclusion, quantitative MRD monitoring seems to be mandatory to assure safe and effective immunotherapy in the context of alloSCT for CLL, which should, however, be best performed within clinical studies.
Item Description:Gesehen am 03.06.2022
Physical Description:Online Resource
ISSN:1532-1681
DOI:10.1016/j.blre.2011.01.001

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