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机构地区:[1]青岛医学院
出 处:《青岛医学院学报》1997年第4期296-298,共3页Acta Academiae Medicinae Qingdao Universitatis
基 金:青岛市科委资助
摘 要:①目的探讨急性淋巴细胞白血病(ALL)微量残留病(MRD)检测的临床意义。②方法应用筑巢式多聚酶链反应(nestedPCR)对32例ALL进行T细胞受体(TCR)Vδ2Dδ3基因重排检测。③结果18例B系ALL中有15例(72.2%)、4例T系ALL中有1例(25.0%)存在TCRVδ2Dδ3基因重排。同时对16例进行39例次微量残留病动态监测,其中6例MRD-PCR阴性病人随访5.17~16.17年,无1例复发;10例MRD-PCR阳性者,2例分别于阳性后0.25,1.00年骨髓复发,1例有复发倾向,余7例随访4.33~6.25年无复发。④结论MRD-PCR阴性者预后良好,可望长期生存,治疗时应以MRD-PCR转阴为停止化疗的可靠指标,对MRD-PCR阳性者应定期监测MRD变化,结合病人情况进行综合评价。Objective To investigate the significance of serial monitoring of minimal residual disease (MRD) in patients with acute lymphoblastic leukemia (ALL). Methods Bone marrow samples of 32 patients were examined using nested polymerase chain reaction (PCR) for detecting Vδ2Dδ3 rearrangement of T cell receptor (TCR) gene. Results Fifteen out of 18 B cell ALL patient(72.2%) and 1 out of 4 T cell ALL patients(25.0%) showed Vδ2Dδ3 gene rearrangement. Sixteen out of 39 cases were detected for MRD. The six MRDPCR negative patients remained long term complete remission (CR) (range 5.17 to 16.17 years). Among the ten MRDPCR positive patients, seven patients remained CR for a long term (range 4.33 to 6.25 years), two patients had bone marrow relapse at three and twelve months after MRD detection. Three cases had central nervous system leukemia (CNSL) or testicular leukemia (TL) without remarkable relationship with PCR results. Conclusion The negative MRDPCR indicate a better outcome and should be regarded as an index of ceasing chemotherapy. The exist of detectable MRD is not sufficent to assure the impending relapse and require periodically monitoring with PCR and other valuable strategy.
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