Department of Hematology, Faculty of Medicine, University of Medicine and Pharmacy at Ho Chi Minh City, Ho Chi Minh City, Vietnam.
Department of Hematology, Cho Ray Hospital, Ho Chi Minh City, Vietnam.
Asian Pac J Cancer Prev. 2023 May 1;24(5):1789-1795. doi: 10.31557/APJCP.2023.24.5.1789.
The cytogenetic characteristics are important factors for risk stratification at diagnosis of acute myeloid leukemia (AML); however, cytogenetic profile of Vietnamese patients with AML remains undetermined. In this study, we present the chromosomal data of de novo AML patients in Southern Vietnam.
We performed cytogenetic testing for 336 AML patients using G banding. If the patients had suspected abnormalities, fluorescence in situ hybridization with probes of inv(3)(q21q26)/t(3;3)(q21;q26), 5q31, 7q31, t(8;21)(q21.3;q22), 11q23, t(15;17)(q24;q21), inv(16)(p13q22)/t(16;16)(p13;q22)were analyzed. Patients without above aberrations or with normal karyotype were tested by fluorescence in situ hybridization using probe 11q23.
We found that the median age was 39 years. According to French - American - British classification, AML-M2 is the most frequent type with 35.1%. Chromosomal abnormalities were detected in 208 cases, accounting for 61.9%. Among structural abnormalities, t(15;17) was the most common (19.6%), followed by t(8;21) and inv (16)/t(16;16) in 10.1% and 6.2%, respectively. In perspective of chromosomal numerical abnornmalities, loss of sex chromosomes are the most common (7.7%), followed by +8 in 6.8%, -7/del(7q) in 4.4%, +21 in 3.9% and -5/del (5q) in 2.1%. The prevalence of addditional cytogenetic aberrations accompanying with t(8;21) and inv(16)/t(16;16) were 82.4% and 52.4%, repectively. None of +8 cases was associated with t(8;21). Regarding cytogenetic risk assessment according to European Leukemia Net 2017, there were 121 (36%) patients in favorable-risk, 180 (53.6%) in intermediate-risk and 35 (10.4%) in adverse-risk group.
In conclusion, this is the first comprehensive cytogenetic profile of Vietnamese patients diagnosed with de novo AML, which helps clinical doctors in prognostic classification for AML patients in Southern Vietnam.
细胞遗传学特征是急性髓细胞白血病(AML)诊断时进行风险分层的重要因素;然而,越南 AML 患者的细胞遗传学特征仍未确定。本研究介绍了越南南部初诊 AML 患者的染色体数据。
我们对 336 例 AML 患者进行了 G 显带染色体核型分析。如果患者有可疑异常,我们会用探针 inv(3)(q21q26)/t(3;3)(q21;q26)、5q31、7q31、t(8;21)(q21.3;q22)、11q23、t(15;17)(q24;q21)、inv(16)(p13q22)/t(16;16)(p13;q22)进行荧光原位杂交(FISH)检测。无上述异常或核型正常的患者用探针 11q23 进行 FISH 检测。
我们发现中位年龄为 39 岁。根据法美英分类,AML-M2 是最常见的类型,占 35.1%。208 例患者发现染色体异常,占 61.9%。在结构异常中,t(15;17)最为常见(19.6%),其次是 t(8;21)和 inv(16)/t(16;16),分别占 10.1%和 6.2%。在染色体数目异常方面,性染色体丢失最为常见(7.7%),其次是+8(6.8%)、-7/del(7q)(4.4%)、+21(3.9%)和-5/del(5q)(2.1%)。t(8;21)和 inv(16)/t(16;16) 患者的附加细胞遗传学异常发生率分别为 82.4%和 52.4%。没有+8 病例与 t(8;21)相关。根据 2017 年欧洲白血病网络(European Leukemia Net)的标准,121 例(36%)患者为低危、180 例(53.6%)为中危、35 例(10.4%)为高危。
总之,这是越南初诊 AML 患者的首个全面细胞遗传学特征,有助于越南南部 AML 患者的临床医生进行预后分类。