Kagita Sailaja, Jiwtani Sangeeta, Uppalapati Srihari, Linga Vijay Gandhi, Gundeti Sadasivudu, Digumarti Raghunadharao
Nizams Institute of Medical Sciences, Punjagutta, Hyderabad, 500082, Andhra Pradesh, India.
Tumour Biol. 2014 May;35(5):4443-6. doi: 10.1007/s13277-013-1585-2. Epub 2014 Jan 12.
Imatinib is the frontline therapy for chronic myeloid leukemia (CML) management. Most of the CML patients achieve major responses, but a proportion (nearly 25-35%) of them develop drug resistance. Molecular monitoring using quantitative real-time PCR at regular intervals according to European LeukemiaNet (ELN) helps in the assessment of long-term outcomes in imatinib-treated CML patients. Eighty-four CML patient samples (42 at diagnosis and 42 at 3-month intervals from the same patients) were analyzed for Bcr-Abl transcript levels. Quantification results revealed that the patients with <10% Bcr-Abl levels at 3 months had higher rates of complete cytogenetic response (CCyR) and optimal responses compared to patients with >10% Bcr-Abl levels (P < 0.0001). Patients with >10% Bcr-Abl levels were found to have 25.0% of suboptimal response and 3.57% of failure to imatinib at standard dose. Hence, the present study confirms that early molecular monitoring at 3 months after imatinib initiation helps in predicting the concurrent cytogenetic response and treatment optimization in CML patients.
伊马替尼是慢性髓性白血病(CML)治疗的一线疗法。大多数CML患者能实现主要缓解,但其中一部分患者(近25%-35%)会产生耐药性。根据欧洲白血病网络(ELN)的建议,定期使用定量实时PCR进行分子监测有助于评估伊马替尼治疗的CML患者的长期预后。对84份CML患者样本(42份诊断时样本以及来自同一患者每隔3个月的42份样本)进行了Bcr-Abl转录水平分析。定量结果显示,与Bcr-Abl水平>10%的患者相比,3个月时Bcr-Abl水平<10%的患者完全细胞遗传学缓解(CCyR)率和最佳缓解率更高(P < 0.0001)。发现Bcr-Abl水平>10%的患者有25.0%的次优缓解,以及3.57%的标准剂量伊马替尼治疗失败。因此,本研究证实,伊马替尼开始治疗3个月时进行早期分子监测有助于预测CML患者的同时细胞遗传学缓解情况和治疗优化。