Sansone R, Di Martino D, Lanino E, Dini G, Massimo L, Tonini G P
Popul. Genetics Sect., Natl. Cancer Inst., Genova, Italy.
Bone Marrow Transplant. 1991;7 Suppl 3:133-5.
From an extended series neuroblastoma cases evaluated for MYCN amplification (MNA) at the "G. Gaslini" Hospital 15 (4 with and 11 without NMA) underwent myeloablative therapy and bone marrow transplantation (MAT-ABMT). Such cases ranged in age at diagnosis from 13 months to 7 years and were followed up at least 8 months after MAT-ABMT. MNA was present in 2/10 cases dead for disease, in 0/1 cases alive with disease, and in 2/4 cases presently in complete clinical remission. This preliminary evidence would discourage to consider MNA as a marker capable of predicting the final outcome of patients with metastatic Nb.
在“G. Gaslini”医院对一系列接受MYCN扩增(MNA)评估的神经母细胞瘤病例进行研究,其中15例(4例有MNA,11例无MNA)接受了清髓性治疗和骨髓移植(MAT-ABMT)。这些病例诊断时的年龄在13个月至7岁之间,在MAT-ABMT后至少随访8个月。MNA在2/10例死于疾病的病例中存在,在0/1例疾病存活的病例中存在,在2/4例目前处于完全临床缓解的病例中存在。这一初步证据不支持将MNA视为能够预测转移性神经母细胞瘤患者最终结局的标志物。