Genetic Profiles and Risk Stratification in Adult De Novo Acute Myeloid Leukaemia in Relation to Age, Gender, and Ethnicity: A Study from Malaysia

Hitherto, no data describing the heterogeneity of genetic profiles and risk stratifications of adult acute myeloid leukaemia (AML) in Southeast Asia are reported. This study assessed genetic profiles, Moorman’s hierarchical classification, and ELN 2017-based risk stratifications in relation to age,...

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Main Authors: Angeli Ambayya, Anthony V. Moorman, Jameela Sathar, Jeyanthy Eswaran, Sarina Sulong, Rosline Hassan
Format: Article
Language:English
Published: MDPI AG 2021-12-01
Series:International Journal of Molecular Sciences
Subjects:
Online Access:https://www.mdpi.com/1422-0067/23/1/258
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author Angeli Ambayya
Anthony V. Moorman
Jameela Sathar
Jeyanthy Eswaran
Sarina Sulong
Rosline Hassan
author_facet Angeli Ambayya
Anthony V. Moorman
Jameela Sathar
Jeyanthy Eswaran
Sarina Sulong
Rosline Hassan
author_sort Angeli Ambayya
collection DOAJ
description Hitherto, no data describing the heterogeneity of genetic profiles and risk stratifications of adult acute myeloid leukaemia (AML) in Southeast Asia are reported. This study assessed genetic profiles, Moorman’s hierarchical classification, and ELN 2017-based risk stratifications in relation to age, gender, and ethnicity in Malaysian adult AML patients. A total of 854 AML patients: male (52%), female (48%) were recruited comprising three main ethnic groups: Malays (59%), Chinese (32%) and Indians (8%). Of 307 patients with abnormal karyotypes: 36% exhibited translocations; 10% deletions and 5% trisomies. The commonest genotype was FLT3-ITD-NPM1wt (276/414; 66.7%). ELN 2017 risk stratification was performed on 494 patients, and 41% were classified as favourable, 39% as intermediate and 20% as adverse groups. More females (47%) were in the favourable risk group compared to males (37%), whereas adverse risk was higher in patients above 60 (24%) of age compared to below 60 (18%) patients. We observed heterogeneity in the distribution of genetic profiles and risk stratifications between the age groups and gender, but not among the ethnic groups. Our study elucidated the diversity of adult AML genetic profiles between Southeast Asians and other regions worldwide.
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spelling doaj.art-8bc076769293404b91baad1de19fe42d2023-11-23T11:37:14ZengMDPI AGInternational Journal of Molecular Sciences1661-65961422-00672021-12-0123125810.3390/ijms23010258Genetic Profiles and Risk Stratification in Adult De Novo Acute Myeloid Leukaemia in Relation to Age, Gender, and Ethnicity: A Study from MalaysiaAngeli Ambayya0Anthony V. Moorman1Jameela Sathar2Jeyanthy Eswaran3Sarina Sulong4Rosline Hassan5School of Medical Sciences, Health Campus, Universiti Sains Malaysia, Kubang Kerian 15159, Kelantan, MalaysiaTranslational and Clinical Research Institute, Newcastle University, Newcastle upon Tyne NE2 4HH, UKClinical Haematology Referral Laboratory, Haematology Department, Hospital Ampang, Ampang 68000, Selangor, MalaysiaTranslational and Clinical Research Institute, Newcastle University, Newcastle upon Tyne NE2 4HH, UKSchool of Medical Sciences, Health Campus, Universiti Sains Malaysia, Kubang Kerian 15159, Kelantan, MalaysiaSchool of Medical Sciences, Health Campus, Universiti Sains Malaysia, Kubang Kerian 15159, Kelantan, MalaysiaHitherto, no data describing the heterogeneity of genetic profiles and risk stratifications of adult acute myeloid leukaemia (AML) in Southeast Asia are reported. This study assessed genetic profiles, Moorman’s hierarchical classification, and ELN 2017-based risk stratifications in relation to age, gender, and ethnicity in Malaysian adult AML patients. A total of 854 AML patients: male (52%), female (48%) were recruited comprising three main ethnic groups: Malays (59%), Chinese (32%) and Indians (8%). Of 307 patients with abnormal karyotypes: 36% exhibited translocations; 10% deletions and 5% trisomies. The commonest genotype was FLT3-ITD-NPM1wt (276/414; 66.7%). ELN 2017 risk stratification was performed on 494 patients, and 41% were classified as favourable, 39% as intermediate and 20% as adverse groups. More females (47%) were in the favourable risk group compared to males (37%), whereas adverse risk was higher in patients above 60 (24%) of age compared to below 60 (18%) patients. We observed heterogeneity in the distribution of genetic profiles and risk stratifications between the age groups and gender, but not among the ethnic groups. Our study elucidated the diversity of adult AML genetic profiles between Southeast Asians and other regions worldwide.https://www.mdpi.com/1422-0067/23/1/258cytogenetickaryotypeacute myeloid leukaemiageneticsELN 2017
spellingShingle Angeli Ambayya
Anthony V. Moorman
Jameela Sathar
Jeyanthy Eswaran
Sarina Sulong
Rosline Hassan
Genetic Profiles and Risk Stratification in Adult De Novo Acute Myeloid Leukaemia in Relation to Age, Gender, and Ethnicity: A Study from Malaysia
International Journal of Molecular Sciences
cytogenetic
karyotype
acute myeloid leukaemia
genetics
ELN 2017
title Genetic Profiles and Risk Stratification in Adult De Novo Acute Myeloid Leukaemia in Relation to Age, Gender, and Ethnicity: A Study from Malaysia
title_full Genetic Profiles and Risk Stratification in Adult De Novo Acute Myeloid Leukaemia in Relation to Age, Gender, and Ethnicity: A Study from Malaysia
title_fullStr Genetic Profiles and Risk Stratification in Adult De Novo Acute Myeloid Leukaemia in Relation to Age, Gender, and Ethnicity: A Study from Malaysia
title_full_unstemmed Genetic Profiles and Risk Stratification in Adult De Novo Acute Myeloid Leukaemia in Relation to Age, Gender, and Ethnicity: A Study from Malaysia
title_short Genetic Profiles and Risk Stratification in Adult De Novo Acute Myeloid Leukaemia in Relation to Age, Gender, and Ethnicity: A Study from Malaysia
title_sort genetic profiles and risk stratification in adult de novo acute myeloid leukaemia in relation to age gender and ethnicity a study from malaysia
topic cytogenetic
karyotype
acute myeloid leukaemia
genetics
ELN 2017
url https://www.mdpi.com/1422-0067/23/1/258
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