Klin Padiatr 2013; 225(S 01): S40-S44
DOI: 10.1055/s-0033-1337962
Zum 80. Geburtstag von Prof. Riehm
© Georg Thieme Verlag KG Stuttgart · New York

Molekulargenetischer Nachweis minimaler Resterkrankung (minimal residual disease, MRD) bei Kindern mit akuter lymphoblastischer Leukämie

Moleculargenetic Detection of Minimal Residual Disease (MRD) in Children with Acute Lymphoblastic Leukemia
R. Koehler
1   Institut für Humangenetik, Universität Heidelberg, Heidelberg (Prof. Dr. C. R. Bartram, Dr. phil. nat. R. Köhler)
,
C. R. Bartram
1   Institut für Humangenetik, Universität Heidelberg, Heidelberg (Prof. Dr. C. R. Bartram, Dr. phil. nat. R. Köhler)
› Author Affiliations
Further Information

Publication History

Publication Date:
22 May 2013 (online)

Zusammenfassung

Die Behandlung der akuten lymphatischen Leukämie (ALL) erlaubt heute im Kindes- und Jugendalter eine Heilungsrate von über 80%. Der Nachweis von minimaler Resterkrankung (minimal residual disease, MRD) mittels molekulargenetischer Methoden eröffnet im Vergleich zu konventionellen klinischen und biologischen Parametern deutlich sensitivere Ansätze, um das individuelle Therapieansprechen zu beurteilen. Hier sollen die molekularen Grundlagen und die technische Entwicklung im Kontext der BFM-Studiengruppe dargestellt werden.

Abstract

The treatment of acute lymphoblastic leukemia (ALL) in childhood and adolescence achieves nowadays cure rates of more than 80%. The detection of minimal residual disease (MRD) via moleculargenetic methods provides – in comparison with conventional clinical and biological parameters – much more sensitive approaches to monitor individual treatment response. Here we will discuss the molecular background and technical developments in the framework of the BFM-study group.

 
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