Pession A, De Bernardi B, Perri P, Mazzocco K, Rondelli R, Nigro M, Iolascon A, Forni M, Basso G, Conte M
Dipartimento di Biologia, Università di Bologna, Italia.
Pediatr Med Chir. 1994 May-Jun;16(3):211-8.
Of 567 children with neuroblastoma diagnosed between November 1984 and May 1993 in 21 Italian institutions, 235 (41%) have been evaluated for MYCN oncogene amplification. The amplification (3 or more copies of the gene) was found in 39 patients (17%) and was more frequent in patients aged more than one year, abdominal primary site of the tumor, advanced stages, normal urinary excretion of vanillylmandelic acid (VMA), and high level of LDH, NSE and ferritin. The five-year survival of the 235 patients (62%) was significantly better in patients with normal copy number of MYCN (69% versus 29%). By correlating genomic amplification with clinical and biochemical characteristics, MYCN amplification was found associated with a worse prognosis even when patients were subdivided for age (under and above one year), disease extension (localized operable, localized but inoperable, and disseminated) with exception for Stage IV-S, VMA and homovanillic acid excretion, serum levels of NSE and ferritin, but not of LDH. These data confirm the unfavourable prognostic meaning of MYCN amplification, but are unable to define if it represents a new independent variable.
在1984年11月至1993年5月期间,意大利21家机构诊断出的567例神经母细胞瘤患儿中,有235例(41%)接受了MYCN癌基因扩增评估。在39例患者(17%)中发现了扩增(该基因有3个或更多拷贝),且在年龄超过1岁、肿瘤原发于腹部、处于晚期、香草扁桃酸(VMA)尿排泄正常、乳酸脱氢酶(LDH)、神经元特异性烯醇化酶(NSE)和铁蛋白水平高的患者中更常见。235例患者(62%)的五年生存率在MYCN拷贝数正常的患者中显著更高(69%对29%)。通过将基因组扩增与临床和生化特征相关联,发现即使将患者按年龄(1岁以下和1岁以上)、疾病分期(局限性可手术、局限性但不可手术和播散性,IV-S期除外)、VMA和高香草酸排泄、NSE和铁蛋白血清水平(但不包括LDH)进行细分,MYCN扩增仍与较差的预后相关。这些数据证实了MYCN扩增的不良预后意义,但无法确定它是否代表一个新的独立变量。