Risks of leukaemia and solid tumours in individuals with Down's syndrome

被引:585
作者
Hasle, H [1 ]
Clemmensen, IH
Mikkelsen, M
机构
[1] Aarhus Univ Hosp Skejby, Dept Paediat, DK-8200 Aarhus N, Denmark
[2] Danish Canc Soc, Inst Canc Epidemiol, Copenhagen, Denmark
[3] John F Kennedy Inst, DK-2600 Glostrup, Denmark
关键词
D O I
10.1016/S0140-6736(99)05264-2
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Individuals with Down's syndrome have a greater risk for leukaemia than the general population, but reliable estimates of the age-specific risk are lacking and little is known about the risk of solid tumours. Methods We identified 2814 individuals with Down's syndrome from the Danish Cytogenetic Register, and linked the data to the Danish Cancer Registry. The number of person-years at risk was 48 453. Standardised incidence ratio (SIR) and 95% CI were calculated of the basis of cancer rates specific for age and sex in the general population. Findings 60 cases of cancer were found, with 49.8 expected (SIR 1.20 [95% CI 0.92-1.55]). Leukaemia constituted 60% of cases of malignant disease overall and 97% of cases in children. The SIR for leukaemia varied with age, being 56 (38-81) at age 0-4 years and 10 (4-20) at 5-29 years. No cases of leukaemia were seen after the age of 29 years. The SIR for acute myeloid leukaemia was 3.8 (1.7-8.4) times higher than that for acute lymphoblastic leukaemia in children aged 0-4 years. The cumulative risk for leukaemia by the age of 5 years was 2.1% and that by 30 years was 2.7%. Only 24 solid tumours were seen, with 47.8 expected (0.50 [0.32-0.75]). No cases of breast cancer were found, with 7.3 expected (p=0.0007). Higher than expected numbers of testicular cancers, ovarian cancers, and retinoblastomas were seen but were not significant. Intrepretation The occurrence of cancer in Down's syndrome is unique with a high risk of leukaemia in children and a decreased risk of solid tumours in all age-groups. The distinctive pattern of malignant diseases may provide clues in the search for leukaemogenic genes and tumour-suppressor genes on chromosome 21.
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页码:165 / 169
页数:5
相关论文
共 46 条
  • [1] CLONAL HEMATOLOGIC DISORDERS IN DOWN-SYNDROME - A REVIEW
    AVETLOISEAU, H
    MECHINAUD, F
    HAROUSSEAU, JL
    [J]. JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY, 1995, 17 (01) : 19 - 24
  • [2] DOWNS-SYNDROME - TRANSIENT ABNORMAL MYELOPOIESIS AND ACUTE-LEUKEMIA
    BAIN, B
    [J]. LEUKEMIA & LYMPHOMA, 1991, 3 (5-6) : 309 - &
  • [3] MORTALITY AND CAUSE OF DEATH IN DOWNS-SYNDROME
    BALARAJAN, R
    DONNAN, SPB
    ADELSTEIN, AM
    [J]. JOURNAL OF EPIDEMIOLOGY AND COMMUNITY HEALTH, 1982, 36 (02) : 127 - 129
  • [4] BENTLEY D, 1975, PEDIATRICS, V56, P131
  • [5] SOD2 - A NEW TYPE OF TUMOR-SUPPRESSOR GENE
    BRAVARD, A
    SABATIER, L
    HOFFSCHIR, F
    RICOUL, M
    LUCCIONI, C
    DUTRILLAUX, B
    [J]. INTERNATIONAL JOURNAL OF CANCER, 1992, 51 (03) : 476 - 480
  • [6] APOPTOSIS AND INCREASED GENERATION OF REACTIVE OXYGEN SPECIES IN DOWNS-SYNDROME NEURONS IN-VITRO
    BUSCIGLIO, J
    YANKNER, BA
    [J]. NATURE, 1995, 378 (6559) : 776 - 779
  • [7] Intracranial germ cell tumors in children with and without Down syndrome
    Chik, KW
    Li, CK
    Shing, MMK
    Leung, TF
    Yuen, PMP
    [J]. JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY, 1999, 21 (02) : 149 - 151
  • [8] DelaTorre R, 1996, EXPERIENTIA, V52, P871
  • [9] FABIA J, 1970, PEDIATRICS, V45, P60
  • [10] FESTER A, 1986, CANCER GENET CYTOGEN, V20, P109