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慢性髓性白血病患者的早期分子反应可预测未来的反应状态。

Early molecular response in chronic myeloid leukemia patients predicts future response status.

作者信息

Kagita Sailaja, Jiwtani Sangeeta, Uppalapati Srihari, Linga Vijay Gandhi, Gundeti Sadasivudu, Digumarti Raghunadharao

机构信息

Nizams Institute of Medical Sciences, Punjagutta, Hyderabad, 500082, Andhra Pradesh, India.

出版信息

Tumour Biol. 2014 May;35(5):4443-6. doi: 10.1007/s13277-013-1585-2. Epub 2014 Jan 12.

Abstract

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.

摘要

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。

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