Xing Wen, Gu Bai-Wei, Zhu Yong-Mei, Jiang Chun-Lei, Zhao Rui-Hua, Wang Ai-Hua, Sun Hui-Ping, Li Jun-Min, Shen Zhi-Xiang, Chen Zhu, Chen Sai-Juan
Shanghai Institute of Hematology, State Key Lab of Medical Genomics, Ruijin Hospital Affiliated to Shanghai Second Medical University, Shanghai 200025, China.
Zhonghua Yi Xue Za Zhi. 2005 Feb 23;85(7):453-7.
To investigate the effect of real-time quantitative reverse transcriptase polymerase chain reaction (RT-PCR) approach in chronic myeloid leukemia (CML) for detecting the minimal residual disease (MRD) or monitoring the treatment response and predicting the prognosis.
Fifty-six CML patients, 39 males and 17 females, aged 39 (16 approximately 66), with disease history and frozen RNA specimens were studied, 31 of which were in the incipient chronic phase, 7 in the accelerated phase, and 17 in the rapidly progressing phase. Three or more frozen RNA specimens collected before and after treatment were preserved in 11 of the patients. Breakpoint cluster region-Abelson murine leukemia viral oncogene (BCR-ABL) of the patients in different CML stages was analyzed by RT-PCR approach.
The BCR-ABL transcript of those patients remaining in chronic period after treatment decreased to 1/3 that of the baseline level six months after the initiation of treatment and then remained at that level. The BCR-ABL transcript of those in which progressing change occurred increased when such change occurred. After allogeneic transplantation of peripheral blood stem cells the BCR-ABL level decreased significantly. The median DoseN in the 17 progressing patients was 10 492, significantly higher than those of the 31 patients in chronic phase (5920) and in the 7 patients in accelerated phase (4444, both P < 0.05). The minimal residual disease and the treatment response were closely associated with the level and its variation of BCR-ABL transcripts, the transcripts level in blastic crisis was significantly higher than that in chronic phase or accelerated phase.
Real-time quantitative RT-PCR is reliable and can be used to detect the minimal residual disease, monitor the treatment outcome, and predicting blastic crisis.
探讨实时定量逆转录聚合酶链反应(RT-PCR)方法在慢性髓性白血病(CML)中检测微小残留病(MRD)、监测治疗反应及预测预后的作用。
研究56例CML患者,男39例,女17例,年龄39岁(16~66岁),有疾病史及冻存RNA标本,其中31例处于慢性期初期,7例处于加速期,17例处于急变期。11例患者保存了治疗前后采集的3份或更多冻存RNA标本。采用RT-PCR方法分析不同CML分期患者的断点簇集区-阿贝尔逊鼠白血病病毒癌基因(BCR-ABL)。
治疗后仍处于慢性期的患者,其BCR-ABL转录本在治疗开始6个月后降至基线水平的1/3,随后维持在该水平。发生病情进展变化的患者,其BCR-ABL转录本在变化发生时升高。异基因外周血干细胞移植后BCR-ABL水平显著降低。17例进展期患者的中位DoseN为10492,显著高于31例慢性期患者(5920)和7例加速期患者(4444,P均<0.05)。微小残留病及治疗反应与BCR-ABL转录本水平及其变化密切相关,急变期的转录本水平显著高于慢性期或加速期。
实时定量RT-PCR可靠,可用于检测微小残留病、监测治疗效果及预测急变。