Open Access

Cytogenetic characteristics of 665 patients with myelodysplastic syndrome in China: A single‑center report

  • Authors:
    • Xueying Wang
    • Weiyi Liu
    • Mingjing Wang
    • Teng Fan
    • Yumeng Li
    • Xiaoqing Guo
    • Xiupeng Yang
    • Hongzhi Wang
    • Haiyan Xiao
    • Shanshan Zhang
    • Richeng Quan
    • Chi Liu
    • Xudong Tang
    • Yan Lv
    • Zhuo Chen
    • Liu Li
    • Yonggang Xu
    • Rou Ma
    • Xiaomei Hu
  • View Affiliations

  • Published online on: December 17, 2020     https://doi.org/10.3892/ol.2020.12387
  • Article Number: 126
  • Copyright: © Wang et al. This is an open access article distributed under the terms of Creative Commons Attribution License.

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Abstract

The karyotype is highly important for diagnosis and prognosis in myelodysplastic syndrome (MDS). The objective of the present study was to investigate the cytogenetic characteristics of patients with MDS in China. The karyotypes of 665 Chinese patients with MDS were analyzed, and it was identified that 298 cases (298/665, 44.8%) had abnormal karyotypes. Among the 298 patients with abnormal karyotypes, the 75 patients with trisomy 8 (+8) constituted the most common subset (75/298, 25.2%). The incidence of abnormal karyotypes was significantly higher in patients who were ≥51 years old compared with those <51 years old, (54.8 vs. 34.7%, respectively; P<0.05). Based on World Health Organization (WHO) classification‑based Prognostic Scoring System (WPSS) criteria, the incidence of poor‑prognosis karyotypes was significantly higher (17.4 vs. 5.4%; P<0.05) in the older patient group, and based on the Revised International Prognostic Scoring System (IPSS‑R) criteria, the incidence of poor‑/very poor‑prognosis karyotypes was also significantly higher (17.4 vs. 6.6%; P<0.05) in patients ≥51 years old compared with younger ones. Based on the WHO classification of MDS subtypes, the incidence of abnormal karyotypes in patients with high percentages of bone marrow (BM) blasts [excess blasts (EB)‑I + EB‑II, ≥5% blasts] was significantly higher than that in patients with low percentages of BM blasts (those with single lineage dysplasia + multilineage dysplasia, <5% blasts) (62.5 vs. 36.0%; P<0.05). The incidence of poor‑prognosis karyotypes based on WPSS criteria was significantly higher in patients with high percentages of BM blasts than those with low percentages (22.0 vs. 6.9%, respectively; P<0.05), and the incidence of poor‑/very poor‑prognosis karyotypes based on IPSS‑R criteria was also significantly higher (23.0 vs. 7.4%, respectively; P<0.05). These results demonstrate that +8 is the most common abnormal karyotype in Chinese patients with MDS. Age and the percentage of BM blasts are associated with the incidence of both abnormal karyotypes and karyotypes with poor prognosis. The results of cytogenetic abnormalities in this study will supplement the data on patients of MDS in China.
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Copy and paste a formatted citation
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Spandidos Publications style
Wang X, Liu W, Wang M, Fan T, Li Y, Guo X, Yang X, Wang H, Xiao H, Zhang S, Zhang S, et al: Cytogenetic characteristics of 665 patients with myelodysplastic syndrome in China: A single‑center report. Oncol Lett 21: 126, 2021
APA
Wang, X., Liu, W., Wang, M., Fan, T., Li, Y., Guo, X. ... Hu, X. (2021). Cytogenetic characteristics of 665 patients with myelodysplastic syndrome in China: A single‑center report. Oncology Letters, 21, 126. https://doi.org/10.3892/ol.2020.12387
MLA
Wang, X., Liu, W., Wang, M., Fan, T., Li, Y., Guo, X., Yang, X., Wang, H., Xiao, H., Zhang, S., Quan, R., Liu, C., Tang, X., Lv, Y., Chen, Z., Li, L., Xu, Y., Ma, R., Hu, X."Cytogenetic characteristics of 665 patients with myelodysplastic syndrome in China: A single‑center report". Oncology Letters 21.2 (2021): 126.
Chicago
Wang, X., Liu, W., Wang, M., Fan, T., Li, Y., Guo, X., Yang, X., Wang, H., Xiao, H., Zhang, S., Quan, R., Liu, C., Tang, X., Lv, Y., Chen, Z., Li, L., Xu, Y., Ma, R., Hu, X."Cytogenetic characteristics of 665 patients with myelodysplastic syndrome in China: A single‑center report". Oncology Letters 21, no. 2 (2021): 126. https://doi.org/10.3892/ol.2020.12387