Matthay Katherine K, Brisse Hervé, Couanet Dominique, Couturier Jerome, Bénard Jean, Mosseri Veronique, Edeline Véronique, Lumbroso Jean, Valteau-Couanet Dominique, Michon Jean
Department of Pediatrics, University of California-San Francisco, San Francisco, California 94143, USA.
Cancer. 2003 Jul 1;98(1):155-65. doi: 10.1002/cncr.11448.
Central nervous system (CNS) metastases rarely occur in patients with neuroblastoma, although recent reports suggest an increase in the rate. CNS recurrence may represent a different mechanism of spread than bone and bone marrow metastases and may be associated with unique genetic determinants. Further definition of the radiologic, clinical, and biologic features may provide clues to the predisposing factors and mechanisms of CNS dissemination.
A retrospective analysis of all children ages 0-21 years with Stage IV neuroblastoma who were diagnosed at the Institut Curie and the Institut Gustave-Roussy between 1985 and 2000 was performed with direct review of medical records and magnetic resonance images, computed tomography scans, and iodine-123 or iodine-131 metaiodobenzylguanidine scintiscans (MIBG scans). When tumor tissue was available, genetic analysis was performed using comparative genomic hybridization (CGH).
Of 434 patients with Stage 4 disease, 23 children had the CNS as their site of first recurrence. The estimated risk of CNS recurrence was 8.0% at 3 years, with no significant change in risk over the 15-year period. Eleven patients had isolated CNS recurrences, and the remaining patients developed recurrences concomitantly in other sites. The sites of recurrences were parenchymal (n = 8 patients), parenchymal with meningeal (n = 7 patients), and meningeal alone (n = 8 patients). MIBG scans detected CNS lesions in only 43% of patients. Significant risk factors for CNS recurrence included lumbar puncture at diagnosis, ages 2-3 years, and MYCN gene amplification. Abnormalities that were identified using CGH, in addition to 2p24 amplification in 5/7, included gains of 17q and 18q and losses of 1p, 3p, 10q25-26, and 11q.
The risk of CNS recurrence in patients with neuroblastoma is 8% at 3 years after diagnosis and has not increased in the last 15 years. Because the CNS often is the sole site of recurrence, either it may be a sanctuary site, or the biologic determinants of CNS metastasis may be unique. Elucidation of risk factors and pathogenesis may allow prevention of this fatal event. Cancer 2003;98:155-65.
中枢神经系统(CNS)转移在神经母细胞瘤患者中很少见,尽管最近的报告显示其发生率有所增加。CNS复发可能代表一种与骨和骨髓转移不同的扩散机制,并且可能与独特的遗传决定因素有关。对放射学、临床和生物学特征的进一步界定可能为CNS播散的易感因素和机制提供线索。
对1985年至2000年间在居里研究所和古斯塔夫 - 鲁西研究所诊断为IV期神经母细胞瘤的所有0至21岁儿童进行回顾性分析,直接查阅病历以及磁共振成像、计算机断层扫描和碘 - 123或碘 - 131间碘苄胍闪烁扫描(MIBG扫描)。当有肿瘤组织时,使用比较基因组杂交(CGH)进行遗传分析。
在434例IV期疾病患者中,23名儿童以CNS作为首次复发部位。3年时CNS复发的估计风险为8.0%,在15年期间风险无显著变化。11例患者为孤立性CNS复发,其余患者在其他部位同时出现复发。复发部位为实质型(n = 8例患者)、实质型伴脑膜型(n = 7例患者)和仅脑膜型(n = 8例患者)。MIBG扫描仅在43%的患者中检测到CNS病变。CNS复发的显著危险因素包括诊断时进行腰椎穿刺、年龄2至3岁和MYCN基因扩增。除了5/7的2p24扩增外,使用CGH鉴定出的异常包括17q和18q的增益以及1p、3p、10q25 - 26和11q的缺失。
神经母细胞瘤患者诊断后3年CNS复发风险为8%,在过去15年中未增加。由于CNS常是唯一的复发部位,要么它可能是一个庇护部位,要么CNS转移的生物学决定因素可能是独特的。阐明危险因素和发病机制可能有助于预防这一致命事件。《癌症》2003年;98:155 - 65。