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神经母细胞瘤:一项基于人群的32年研究——对筛查的启示

Neuroblastoma: a 32-year population-based study--implications for screening.

作者信息

Huddart S N, Muir K R, Parkes S, Mann J R, Stevens M C, Raafat F

机构信息

Department of Oncology, Children's Hospital, Birmingham, England.

出版信息

Med Pediatr Oncol. 1993;21(2):96-102. doi: 10.1002/mpo.2950210204.

Abstract

This paper describes a retrospective population-based study of neuroblastoma in the West Midlands Health Authority Region--childhood population 1.12 million (OPCS, census 1981)--in which 239 cases were diagnosed between 1st January 1957 and 31st December 1988. The age standardised rate of tumour incidence has remained constant at 7.2 cases per million children per year. The median age at diagnosis was 2 years with 18% of children presenting before the age of 6 months. Fifty children (21%) presented before the age of one year, and for this group of children, the prognosis has improved significantly over the 32-year period (10 year survival increasing from 63% in 1957-67 to 87% in 1978-88), whereas for the 189 (79%) children who presented after one year of age, the prognosis has remained very poor during the study period (10 year survival 1957-67 = 9.5%, 1978-88 = 8.5%). This study supports the need for a prospective study of mass screening at several intervals rather than only at 6 months of age.

摘要

本文描述了一项基于人群的西米德兰兹郡卫生局辖区神经母细胞瘤回顾性研究——儿童人口为112万(1981年人口普查,人口普查局),在1957年1月1日至1988年12月31日期间诊断出239例病例。肿瘤发病率的年龄标准化率一直保持在每年每百万儿童7.2例。诊断时的中位年龄为2岁,18%的儿童在6个月前发病。50名儿童(21%)在1岁前发病,对于这组儿童,在32年期间预后有显著改善(10年生存率从1957 - 1967年的63%提高到1978 - 1988年的87%),而对于189名(79%)1岁后发病的儿童,在研究期间预后仍然很差(1957 - 1967年10年生存率 = 9.5%,'1978 - 1988年 = 8.5%)。本研究支持有必要进行前瞻性研究,在多个时间间隔进行大规模筛查,而不是仅在6个月大时进行筛查。

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