Hasan Z, Inoue A, Ikeda H, Kamii Y, Obana K, Yokomori K, Tsuchida Y, Hemmi H, Shimatake H
Department of Pediatric Surgery, Faculty of Medicine, University of Tokyo, Japan.
Eur J Pediatr Surg. 1999 Jun;9(3):138-41. doi: 10.1055/s-2008-1072229.
If an unfavorable prognosis is suspected in neuroblastoma, decision on a treatment protocol should be based on the N-myc copy number (12). We already demonstrated that the newly developed competitive polymerase chain reaction (competitive PCR) is a promising method for the determination of the N-myc copy number (6), and have started to use this competitive PCR procedure in neuroblastoma patients, together with fine-needle biopsy in selected cases. Seven children were studied. In one infant of 5 months of age whose tumor was diagnosed before undergoing mass screening for neuroblastoma, the competitive PCR procedure was performed with a fine-needle biopsy, and after obtaining a negative report on N-myc amplification within 48 hours, a regular protocol of treatment could be started without delay. We report that competitive PCR is a rapid and accurate method for the determination of the N-myc copy number, requiring only a small amount of material, and anticipate that competitive PCR will become the procedure of choice for the determination of N-myc copy number in neuroblastoma.
如果怀疑神经母细胞瘤预后不良,治疗方案的决策应基于N - myc拷贝数(12)。我们已经证明,新开发的竞争性聚合酶链反应(竞争性PCR)是一种用于测定N - myc拷贝数的有前景的方法(6),并且已经开始在神经母细胞瘤患者中使用这种竞争性PCR程序,在选定病例中结合细针活检。对7名儿童进行了研究。在一名5个月大的婴儿中,其肿瘤在进行神经母细胞瘤大规模筛查之前被诊断出来,通过细针活检进行了竞争性PCR程序,在48小时内获得N - myc扩增阴性报告后,可立即开始常规治疗方案。我们报告竞争性PCR是一种快速、准确的测定N - myc拷贝数的方法,只需要少量材料,并预计竞争性PCR将成为神经母细胞瘤中测定N - myc拷贝数的首选程序。