Monitoring of minimal residual disease in patients with MLL-AF6 -positive acute myeloid leukaemia by reverse transcriptase polymerase chain reaction
Open Access
- 1 June 2000
- journal article
- research article
- Published by Wiley in British Journal of Haematology
- Vol. 109 (3) , 622-628
- https://doi.org/10.1046/j.1365-2141.2000.02076.x
Abstract
We studied 210 unselected patients with acute myeloid leukaemia (AML) for MLL abnormalities. Twenty‐seven patients (13%) with rearranged MLL genes were identified by means of Southern blot analysis. An MLL–AF6 fusion transcript was detected in six patients by a reverse transcriptase polymerase chain reaction (RT‐PCR) for the MLL–AF6 translocation. Sequence analysis showed fusion of MLL exon 7 as well as exon 6 (two patients) or MLL exon 6 as well as exon 5 (four patients) to AF6 exon 2. In only three patients could the t(6;11) also be identified by cytogenetic and/or fluorescence in situ hybridization (FISH) analysis. The MLL–AF6‐positive patients were monitored by RT‐PCR for a period of 6–33 months. Complete haematological remission (CR) was achieved in all six cases, but was short in 5/6 patients (range 2·6–8·3 months). In these five patients, the MLL–AF6 transcripts were detected in every sample tested after induction and consolidation chemotherapy. One patient received autologous bone marrow transplantation (BMT) which also did not lead to PCR negativity. Intensive salvage therapy was unable to induce a second remission in the relapsed patients. One of the six MLL–AF6‐positive patients achieved a molecular CR. He is still in CR at 33 months after diagnosis. Survival analysis indicates a poor prognosis in MLL–AF6‐positive patients. The median event‐free survival was 6·8 months, the median overall survival 15 months. Persistent PCR positivity was consistently associated with relapse. Thus, RT‐PCR provides a valuable and sensitive tool for the identification of t(6;11)‐positive AML and the monitoring of response to treatment in these patients. The results of RT‐PCR may be useful to evaluate therapeutic procedures and to make treatment decisions, which will enable molecular remissions to be achieved and improve the clinical outcome in this group of patients.Keywords
This publication has 27 references indexed in Scilit:
- Ten novel 11q23 chromosomal partner sitesLeukemia, 1998
- A Randomized, Double-Blind, Placebo-Controlled, Phase III Study of Filgrastim in Remission Induction and Consolidation Therapy for Adults With De Novo Acute Myeloid LeukemiaBlood, 1997
- An Mll–AF9 Fusion Gene Made by Homologous Recombination Causes Acute Leukemia in Chimeric Mice: A Method to Create Fusion OncogenesCell, 1996
- Prevalence and clinical correlations of MLL gene rearrangements in AML- M4/5Blood, 1994
- Acute leukemias of different lineages have similar MLL gene fusions encoding related chimeric proteins resulting from chromosomal translocation.Proceedings of the National Academy of Sciences, 1993
- Acute mixed-lineage leukemia t(4;11)(q21;q23) generates an MLL-AF4 fusion product.Proceedings of the National Academy of Sciences, 1993
- Molecular rearrangements on chromosome 11q23 predominate in infant acute lymphoblastic leukemia and are associated with specific biologic variables and poor outcomeBlood, 1993
- The t(4;11) chromosome translocation of human acute leukemias fuses the ALL-1 gene, related to Drosophila trithorax, to the AF-4 geneCell, 1992
- A trithorax–like gene is interrupted by chromosome 11q23 translocations in acute leukaemiasNature Genetics, 1992
- In situ hybridization ascertains the presence of a translocation t(6;11) in an acute monocytic leukemiaGenes, Chromosomes and Cancer, 1990