Retinoblastoma incidence and survival in European children (1978-1997). Report from the Automated Childhood Cancer Information System project

被引:104
作者
MacCarthy, A.
Draper, G. J.
Steliarova-Foucher, Eva
Kingston, J. E.
机构
[1] Univ Oxford, Childhood Canc Res grp, Oxford OX2 6HJ, England
[2] Int Agcy Res Canc, Descript Epidemiol Grp, F-69372 Lyon 08, France
[3] Barts & London NHS Trust, Retinoblastoma Serv, London EC1A 7BE, England
关键词
cancer; childhood; Europe; registry; incidence; survival; retinoblastoma; trends;
D O I
10.1016/j.ejca.2006.06.003
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Based on 2283 cases of retinoblastoma diagnosed in children aged 0-14 years, incidence and survival in Europe during the period 1978-1997 are described. Data were provided to the Automated Childhood Cancer Information System (ACCIS) from 60 paediatric and general cancer registries. During 1988-1997, the cumulative incidence of retinoblastoma in the ACCIS regions was found to be between 44.2 and 67.9 per million births. The highest incidence was seen in the first year of life. The age-standardised (World standard) incidence rate for the age-range 0-14 years was 4.1 per million. Approximately one-third of cases had bilateral tumours. Overall incidence increased over the period 1978-1997 by 1% per year, as derived from a model adjusted for sex, age group and type of registry (general or paediatric). The 5-year survival rate improved from 89% to 95% during the period covered by the study This improvement was seen in both unilateral and bilateral cases but was significant only for the unilateral tumours. Survival was lower in the East region, although smaller differences were also observed between the other four regions (British isles, North, South and West). Availability and quality of registration data on retinoblastoma need to be improved for effective evaluation of incidence and survival. (c) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2092 / 2102
页数:11
相关论文
共 24 条
  • [1] Second nonocular tumors in survivors of bilateral retinoblastoma - A possible age effect on radiation-related risk
    Abramson, DH
    Frank, CM
    [J]. OPHTHALMOLOGY, 1998, 105 (04) : 573 - 579
  • [2] First-line chemotherapy with local treatment can prevent external-beam irradiation and enucleation in low-stage intraocular retinoblastoma
    Beck, MN
    Balmer, A
    Dessing, C
    Pica, A
    Munier, F
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2000, 18 (15) : 2881 - 2887
  • [3] BERKSON J, 1950, MAYO CLIN P, V25, P270
  • [4] Retinoblastoma: the disease, gene and protein provide critical leads to understand cancer
    DiCiommo, D
    Gallie, BL
    Bremner, R
    [J]. SEMINARS IN CANCER BIOLOGY, 2000, 10 (04) : 255 - 269
  • [5] Lifetime risks of common cancers among retinoblastoma survivors
    Fletcher, O
    Easton, D
    Anderson, K
    Gilham, C
    Jay, M
    Peto, J
    [J]. JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2004, 96 (05): : 357 - 363
  • [6] Postenucleation adjuvant therapy in high-risk retinoblastoma
    Honavar, SG
    Singh, AD
    Shields, CL
    Meadows, AT
    Demirci, H
    Cater, J
    Shields, JA
    [J]. ARCHIVES OF OPHTHALMOLOGY, 2002, 120 (07) : 923 - 931
  • [7] Kalbfleisch JD., 2011, STAT ANAL FAILURE TI
  • [8] Risk of new cancers after radiotherapy in long-term survivors of retinoblastoma: An extended follow-up
    Kleinerman, RA
    Tucker, MA
    Tarone, RE
    Abramson, DH
    Seddon, JM
    Stovall, M
    Li, FP
    Fraumeni, JF
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (10) : 2272 - 2279
  • [9] Kramarova E, 1996, INT J CANCER, V68, P759
  • [10] KROLL ME, 2004, CANCERSTATS MONOGRAP, P63