Department of Pathology, Faculty of Medicine, University Malaya, Lembah Pantai, 50603, Kuala Lumpur, Malaysia.
Clinical Haematology Laboratory, Department of Haematology, Hospital Ampang, Kuala Lumpur, Malaysia.
Int J Hematol. 2011 Apr;93(4):465-473. doi: 10.1007/s12185-011-0796-9. Epub 2011 Mar 9.
The outcome of treating chronic myeloid leukemia (CML) with imatinib mesylate (IM) is inferior when therapy is commenced in late chronic or accelerated phase as compared to early chronic phase. This may be attributed to additional genomic alterations that accumulate during disease progression. We sought to identify such lesions in patients showing suboptimal response to IM by performing array-CGH analysis on 39 sequential samples from 15 CML patients. Seventy-four cumulative copy number alterations (CNAs) consisting of 35 losses and 39 gains were identified. Alterations flanking the ABL1 and BCR genes on chromosomes 9 and 22, respectively, were the most common identified lesions with 5 patients losing variable portions of 9q34.11 proximal to ABL1. Losses involving 1p36, 5q31, 17q25, Y and gains of 3q21, 8q24, 22q11, Xp11 were among other recurrent lesions identified. Aberrations were also observed in individual patients, involving regions containing known leukemia-associated genes; CDKN2A/2B, IKZF1, RB1, TLX1, AFF4. CML patients in late stages of their disease, harbor pre-existing and evolving sub-microscopic CNAs that may influence disease progression and IM response.
伊马替尼治疗慢性髓性白血病(CML)的疗效在慢性期或加速期晚期开始治疗时不如早期慢性期,这可能归因于疾病进展过程中积累的额外基因组改变。我们通过对 15 例 CML 患者的 39 个连续样本进行 array-CGH 分析,旨在确定对伊马替尼反应不佳的患者中的这些病变。确定了 74 个累积拷贝数改变(CNA),包括 35 个缺失和 39 个增益。分别位于染色体 9 和 22 上的 ABL1 和 BCR 基因侧翼的改变是最常见的病变,5 例患者在 ABL1 近端缺失了 9q34.11 的可变部分。1p36、5q31、17q25、Y 的缺失和 3q21、8q24、22q11、Xp11 的增益是其他反复出现的病变之一。个别患者也观察到了异常,涉及含有已知白血病相关基因的区域;CDKN2A/2B、IKZF1、RB1、TLX1、AFF4。疾病晚期的 CML 患者存在预先存在和不断进化的亚微观 CNA,可能影响疾病进展和伊马替尼反应。