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Comparative Study
. 2003 Mar;18(1):13-20.
doi: 10.3904/kjim.2003.18.1.13.

Prognostic value of AML 1/ETO fusion transcripts in patients with acute myelogenous leukemia

Affiliations
Comparative Study

Prognostic value of AML 1/ETO fusion transcripts in patients with acute myelogenous leukemia

Eun Kyung Cho et al. Korean J Intern Med. 2003 Mar.

Abstract

Background: The t (8;21) (q22;q22), which produces the fusion gene AML1/ETO, is associated with relatively good prognosis and, in particular, with a good response to cytosine arabinoside. Analysis of t (8;21) positive leukemic blasts has shown characteristic morphological and immunological features. We performed this study to investigate the incidence of AML1/ETO rearrangement in adult acute myelogenous leukemia (AML), especially in M2 subtype, to make a comparison of clinical, morphological and immunophenotypic characteristics between AML1/ETO rearrangement positive and negative group in patients with AML and to analyze the correlation with other biological parameters.

Methods: From May 1995 to Sept. 2000, fifty-nine patients with AML, including twenty-nine AML-M2, were studied. RNAs were extracted from leukemic cells and reverse transcriptase mediated polymerase chain reaction (RT-PCR) for AML1/ETO fusion transcript was done. Chromosome study, immunophenotypic and clinical characteristics were analyzed and statistical analysis was done.

Results: The incidence of AML1/ETO fusion transcripts was 22.0% in AML and 44.8% in AML-M2. The morphologic finding of bone marrow in AML-M2 showed higher incidence of Auer rods, large blast with prominent golgi and abnormal granules in AML1/ETO positive patients. There was no significant difference of immunophenotype. AML patients with AML1/ETO had a tendency of higher complete remission rate (81.8% vs 56.6%, p = 0.13). The overall survival (median; 82.2 weeks vs 34.4 weeks, p = 0.02) and progression free survival (median; 50.9 weeks vs 20.4 weeks, p = 0.02) of AML1/ETO positive group were longer than those of the negative group in AML. AML-M2 patients with AML1/ETO rearrangement had also a tendency of longer overall survival and progression free survival, although there was no significant difference between both groups.

Conclusion: Our data suggest that AML1/ETO rearrangement is detected frequently in AML, especially M2, and is a favorable prognostic factor. Thus, molecular diagnostic approaches should be used routinely to identify patients with this gentic subtype of AML.

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Figures

Figure 1.
Figure 1.
Detection of AML1/ETO specific transcripts by RT-PCR in AML patients and cell lines. Lane M: length marker ψX174F/Hae III-digest, lane 1 & 4: positive patients, lane 2: K562 cell line, lane 3: primer control (no RNA), lane 5: negative patients.
Figure 2.
Figure 2.
Morphologic finding of AML1/ETO positive and negative patients with AML-M2 (×1,000). (A) AML1/ETO positive patients. There are Auer rod (↑), abnormal granules in leukemic blast. The size of blasts are large and they have prominent golgi. (B) AML1/ETO negative patients. No blasts have Auer rod, eosinophils, abnormal granules and prominent golgi.
Figure 3.
Figure 3.
Overall survival of the AML1/ETO positive and negative group in AML.
Figure 4.
Figure 4.
Progression-free survival of the AML1/ETO positive and negative group in AML.

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