Gupta Ruchi, Rahman Khaliqur, Singh Manish Kumar, Kumari Surabhi, Yadav Geeta, Nityanand Soniya
Department of Hematology, Sanjay Gandhi Post Graduate Institute of Medical Sciences, Lucknow, Uttar Pradesh, India.
Mediterr J Hematol Infect Dis. 2017 Aug 16;9(1):e2017048. doi: 10.4084/MJHID.2017.048. eCollection 2017.
Myelodysplastic syndrome (MDS) is a heterogeneous disorder characterized clinically by the presence of cytopenia/s. Limited data are available about the morphological spectrum and cytogenetic profile of Indian MDS patients. The aim of the study was to ascertain the clinico-pathological, morphological and cytogenetic spectrum of Indian MDS patients.
A retrospective analysis of all patients diagnosed with MDS from June 2012 to December 2016 was performed. Their clinical and laboratory data were collated and reviewed.
A total of 150 patients with primary MDS were evaluated with M: F ratio of 1.6:1 and the median age of 55.5 years. 64% patients presented with pancytopenia and 31% with bicytopenia. Morphologically they included MDS-MLD [63 (42%)], MDS-EB 2, [33 (22%)], MDS-EB 1 [32 (21.3%)], MDS-SLD [13 (8.6%)] and two cases (1.4%) each of MDS-SLD-RS, MDS-MLD-RS, and RCC. An abnormal cytogenetic profile was detected in 50% patients. Complex karyotype was observed to be the commonest abnormality (32.5%), and chromosome 7 was the most frequently involved chromosome. Isolated deletion 5q was seen in 6.9 % cases. Novel translocations like t(9;22)(q11.2;q34.2), t(1;5)(p22;q33), t(1;12)(p34;p11.2) and t(5;7;9)(q13;q32;p22) were observed in addition to other complex abnormalities. The majority of the patients belonged to the high risk IPSS-R prognostic groups (31.4%); followed by intermediate and very high-risk groups, 29% and 24.4% respectively.
The median age of patients in India is a decade younger than the western population. Complex karyotype was observed to be the commonest cytogenetic abnormality, while the frequency of deletion 5q and trisomy 8 was much lower as compared to the west. The majority of the patients were in high to very high IPSS-R risk categories and seventy percent individuals below 40 years showed abnormal karyotype, indicating that Indian MDS patients have high disease burden at a young age and thus more likelihood for leukemic transformation.
骨髓增生异常综合征(MDS)是一种异质性疾病,临床特征为血细胞减少。关于印度MDS患者的形态学谱和细胞遗传学特征的数据有限。本研究的目的是确定印度MDS患者的临床病理、形态学和细胞遗传学谱。
对2012年6月至2016年12月期间所有诊断为MDS的患者进行回顾性分析。整理并回顾他们的临床和实验室数据。
共评估了150例原发性MDS患者,男女比例为1.6:1,中位年龄为55.5岁。64%的患者表现为全血细胞减少,31%表现为两系血细胞减少。形态学上,他们包括MDS-MLD[63例(42%)]、MDS-EB 2[33例(22%)]、MDS-EB 1[32例(21.3%)]、MDS-SLD[13例(8.6%)],以及各2例(1.4%)的MDS-SLD-RS、MDS-MLD-RS和RCC。50%的患者检测到异常细胞遗传学特征。复杂核型被观察到是最常见的异常(32.5%),7号染色体是最常受累的染色体。6.9%的病例可见孤立的5q缺失。除其他复杂异常外,还观察到新的易位,如t(9;22)(q11.2;q34.2)、t(1;5)(p22;q33)、t(1;12)(p34;p11.2)和t(5;7;9)(q13;q32;p22)。大多数患者属于高风险IPSS-R预后组(31.4%);其次是中危和极高危组,分别为29%和24.4%。
印度患者的中位年龄比西方人群小十岁。复杂核型被观察到是最常见的细胞遗传学异常,而5q缺失和8三体的频率与西方相比要低得多。大多数患者处于高至极高的IPSS-R风险类别,40岁以下的个体中有70%显示核型异常,这表明印度MDS患者在年轻时疾病负担较高,因此白血病转化的可能性更大。