CYTOGENETIC ANALYSIS IN SLOVENIAN ACUTE LEUKEMIA PATIENTS

BACKGROUND Modern therapeutic concepts in acute leukemia are based on individual risk stratificationat diagnosis and during follow-up. Cytogenetics plays a central role for classification andfor prognostication in acute myeloid (AML) and considering t(9;22) determination also inacute lymphoblastic l...

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Main Authors: Helena Podgornik, Alenka Prijatelj, Peter Černeič
Format: Article
Language:English
Published: Slovenian Medical Association 2008-04-01
Series:Zdravniški Vestnik
Online Access:http://vestnik.szd.si/index.php/ZdravVest/article/view/881
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spelling doaj-1e15992afc6e4cde82d2e69b0f0896222020-11-25T01:03:09ZengSlovenian Medical AssociationZdravniški Vestnik1318-03471581-02242008-04-0177SUPPI759CYTOGENETIC ANALYSIS IN SLOVENIAN ACUTE LEUKEMIA PATIENTSHelena PodgornikAlenka PrijateljPeter ČerneičBACKGROUND Modern therapeutic concepts in acute leukemia are based on individual risk stratificationat diagnosis and during follow-up. Cytogenetics plays a central role for classification andfor prognostication in acute myeloid (AML) and considering t(9;22) determination also inacute lymphoblastic leukemia (ALL). This method also helps to determine a suitable geneticmarker for later monitoring of minimal residual disease (MRD). Results of standard cytogenetics obtained in our laboratory were analyzed and compared with literature data. METHODS During the last two years cytogenetic analysis was done in 120 adults and children whowere diagnosed with acute leukemia. Bone marrow cells were short-time cultivated to obtain metaphases which were analyzed after G-banding (Giemsa-trypsin). In majority of cases fluorescent in situ hybridization (FISH) was also applied to determine or confirm thesuspected chromosomal aberrations. RESULTS The standard cytogenetics was successful in 90 % of samples. In 70 % of AL patients clonalchromosomal changes were found. Recurrent chromosomal aberrations were determinedwith expected frequency as previously published for other populations. Also the frequencies of patients with a normal karyotype and complex chromosomal changes were in theexpected range. CONCLUSIONS Using molecular cytogenetic and genetic methods a possibility that some of chromosomalchanges were overlooked was considerably minimized. On the basis of the analyzed datawe can be confident that the cytogenetic diagnostic approach in our acute leukemia patients is in accordance with international guidelineshttp://vestnik.szd.si/index.php/ZdravVest/article/view/881
collection DOAJ
language English
format Article
sources DOAJ
author Helena Podgornik
Alenka Prijatelj
Peter Černeič
spellingShingle Helena Podgornik
Alenka Prijatelj
Peter Černeič
CYTOGENETIC ANALYSIS IN SLOVENIAN ACUTE LEUKEMIA PATIENTS
Zdravniški Vestnik
author_facet Helena Podgornik
Alenka Prijatelj
Peter Černeič
author_sort Helena Podgornik
title CYTOGENETIC ANALYSIS IN SLOVENIAN ACUTE LEUKEMIA PATIENTS
title_short CYTOGENETIC ANALYSIS IN SLOVENIAN ACUTE LEUKEMIA PATIENTS
title_full CYTOGENETIC ANALYSIS IN SLOVENIAN ACUTE LEUKEMIA PATIENTS
title_fullStr CYTOGENETIC ANALYSIS IN SLOVENIAN ACUTE LEUKEMIA PATIENTS
title_full_unstemmed CYTOGENETIC ANALYSIS IN SLOVENIAN ACUTE LEUKEMIA PATIENTS
title_sort cytogenetic analysis in slovenian acute leukemia patients
publisher Slovenian Medical Association
series Zdravniški Vestnik
issn 1318-0347
1581-0224
publishDate 2008-04-01
description BACKGROUND Modern therapeutic concepts in acute leukemia are based on individual risk stratificationat diagnosis and during follow-up. Cytogenetics plays a central role for classification andfor prognostication in acute myeloid (AML) and considering t(9;22) determination also inacute lymphoblastic leukemia (ALL). This method also helps to determine a suitable geneticmarker for later monitoring of minimal residual disease (MRD). Results of standard cytogenetics obtained in our laboratory were analyzed and compared with literature data. METHODS During the last two years cytogenetic analysis was done in 120 adults and children whowere diagnosed with acute leukemia. Bone marrow cells were short-time cultivated to obtain metaphases which were analyzed after G-banding (Giemsa-trypsin). In majority of cases fluorescent in situ hybridization (FISH) was also applied to determine or confirm thesuspected chromosomal aberrations. RESULTS The standard cytogenetics was successful in 90 % of samples. In 70 % of AL patients clonalchromosomal changes were found. Recurrent chromosomal aberrations were determinedwith expected frequency as previously published for other populations. Also the frequencies of patients with a normal karyotype and complex chromosomal changes were in theexpected range. CONCLUSIONS Using molecular cytogenetic and genetic methods a possibility that some of chromosomalchanges were overlooked was considerably minimized. On the basis of the analyzed datawe can be confident that the cytogenetic diagnostic approach in our acute leukemia patients is in accordance with international guidelines
url http://vestnik.szd.si/index.php/ZdravVest/article/view/881
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