Kim M, Lee S, Jung C K, Lim J, Cho S G, Kim D W, Kim Y, Han K, Min W S, Kim C C
Department of Laboratory Medicine, College of Medicine, The Catholic University of Korea, Seoul, Korea.
Int J Lab Hematol. 2008 Dec;30(6):508-12. doi: 10.1111/j.1751-553X.2007.00991.x.
We investigated chronic myelogenous leukemia (CML) patients who developed trisomy 8 abnormalities in Philadelphia-negative (Ph-) cells during imatinib mesylate treatment to evaluate the clinical outcome and laboratory features. Of the 470 CML patients, 1.5% (n = 7) developed trisomy 8 chromosomal abnormalities in Ph- cells. The median interval of the first trisomy 8 observation was 12 months. Our follow-up cytogenetic evaluations revealed that six of the patients demonstrated a complete or partial cytogenetic response and that all of the six patients revealed no dysplastic changes following a bone marrow examination. Moreover, the percentage of trisomy 8 in metaphase karyotyping has decreased in five of the seven subjects. In conclusion, these results suggest that the emergence of trisomy 8 in Ph- cells is transient and not related to therapy-related myelodysplasia or acute leukemia.
我们对在甲磺酸伊马替尼治疗期间费城染色体阴性(Ph-)细胞中出现8号染色体三体异常的慢性粒细胞白血病(CML)患者进行了研究,以评估临床结局和实验室特征。在470例CML患者中,1.5%(n = 7)的患者Ph-细胞出现了8号染色体三体异常。首次观察到8号染色体三体的中位间隔时间为12个月。我们的后续细胞遗传学评估显示,其中6例患者表现出完全或部分细胞遗传学缓解,并且这6例患者在骨髓检查后均未发现发育异常改变。此外,7例患者中有5例中期核型分析中8号染色体三体的比例有所下降。总之,这些结果表明,Ph-细胞中8号染色体三体的出现是短暂的,与治疗相关的骨髓发育异常或急性白血病无关。