Suppr超能文献

斯蒂芬·L·甘斯海外讲座。日本神经母细胞瘤的大规模筛查:经验教训与未来方向。

Stephen L. Gans overseas lecture. Mass screening for neuroblastoma in Japan: lessons learned and future directions.

作者信息

Suita Sachiyo

机构信息

Department of Pediatric Surgery, Reproductive and Developmental Medicine, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.

出版信息

J Pediatr Surg. 2002 Jul;37(7):949-54. doi: 10.1053/jpsu.2002.33814.

Abstract

BACKGROUND/PURPOSE: Since 1985, a nationwide mass screening program (MS) for neuroblastoma has been conducted for 6-month-old infants throughout Japan, resulting in the detection of more than 1,900 cases of neuroblastoma. The outcome of these patients has been excellent: more than 97% of them are alive. Yet, several reports suggest that the number of advanced-stage neuroblastoma patients over 1 year of age has not changed substantially. The current report focuses on the 15-year experience with MS of the Kyushu Pediatric Oncology Study Group.

METHODS

The clinical and biological features of neuroblastoms detected (n = 320) and not detected by MS (n = 245) were compared. Regional and national statistics for neuroblastoma before and after 1985 were analyzed using standard epidemiologic measures for the occurrence of disease.

RESULTS

The majority of the MS-positive cases were biologically favorable and had an excellent outcome. In contrast, the majority of non-MS patients in whom neuroblastoma later developed had advanced-stage, unfavorable-prognosis tumors. The overall mortality rate of neuroblastoma in the Kyushu area was not improved by MS.

CONCLUSIONS

The optimal time for screening is the point at which neuroblastomas regressing spontaneously can no longer be detected, but more aggressive disease can be found. A birth cohort study could determine the optimal timing for a second screening. Identification of other new prognostic factors may be required.

摘要

背景/目的:自1985年以来,日本全国针对6个月大婴儿开展了神经母细胞瘤全国大规模筛查项目(MS),已检测出1900多例神经母细胞瘤病例。这些患者的预后非常好:超过97%的患者存活。然而,一些报告表明,1岁以上晚期神经母细胞瘤患者的数量并没有显著变化。本报告重点关注九州儿科肿瘤研究组15年的大规模筛查经验。

方法

比较通过大规模筛查检测出的神经母细胞瘤(n = 320)和未检测出的神经母细胞瘤(n = 245)的临床和生物学特征。使用疾病发生的标准流行病学方法分析1985年前后神经母细胞瘤的区域和全国统计数据。

结果

大多数大规模筛查呈阳性的病例生物学特征良好,预后极佳。相比之下,后来发生神经母细胞瘤的大多数未进行大规模筛查的患者患有晚期、预后不良的肿瘤。大规模筛查并未改善九州地区神经母细胞瘤的总体死亡率。

结论

筛查的最佳时间是自发消退的神经母细胞瘤无法再被检测到,但能发现更具侵袭性疾病的时间点。一项出生队列研究可以确定二次筛查的最佳时机。可能需要识别其他新的预后因素。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验