Increased incidence of cancer in adult Gaucher disease in Western Europe

被引:141
作者
de Fost, M
vom Dahl, S
Weverling, GJ
Brill, N
Brett, S
Häussinger, D
Hollak, CEM
机构
[1] Univ Amsterdam, Acad Med Ctr, Dept Internal Med, NL-1100 DD Amsterdam, Netherlands
[2] Univ Dusseldorf, Div Gastroenterol Hepatol & Infect Dis, D-4000 Dusseldorf, Germany
[3] Univ Amsterdam, Acad Med Ctr, Dept Clin Epidemiol & Biostat, NL-1100 DD Amsterdam, Netherlands
关键词
Gaucher disease; multiple myeloma; hepatocellular carcinoma; incidence; mortality;
D O I
10.1016/j.bcmd.2005.08.004
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The adult form of Gaucher disease (type I GD) is associated with a high prevalence of hypergammaglobulinemia and monoclonal gammopathy of undetermined significance (MGUS). A significantly increased risk of cancer, especially of hematological types, has been found in Ashkenazi-Jewish GD type 1 patients. In this study, incidence and mortality of cancer were assessed in a total of 131 GD patients of mixed ancestry in a population from Western Europe, i.e. 2 Gaucher referral centers in Germany (Dusseldorf) and the Netherlands (Amsterdam). Standardized rate ratios were determined by indirect standardization, using age- and sex-specific incidence and mortality rates of the Dutch population. A total of 14 GD patients of non-Ashkenazi-Jewish descent were identified of whom 5 had a hematologic malignancy. These numbers correspond to an increased risk of cancer of 2.5 (95% CI 1.1-4.7) and an increased risk of hematologic cancer of 12.7 (95% CI 2.6-37.0) among GD patients compared to the general population. In particular, the incidences of multiple myeloma and hepatocellular carcinoma in absence of preexisting cirrhosis were highly elevated, with standardized rate ratios of 51.1 (95% CI 6.2-184) and 141.3 (95% CI 17.1-510.5), respectively. These strongly increased risks on developing cancer suggest that measures for early detection and prevention of hematological and hepatic malignancies in patients with Gaucher type I disease are mandatory. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:53 / 58
页数:6
相关论文
共 45 条
  • [1] DEFICIENT ACTIVITY OF GLUCOCEREBROSIDASE IN URINE FROM PATIENTS WITH TYPE-1 GAUCHER DISEASE
    AERTS, JMFG
    DONKERKOOPMAN, WE
    KOOT, M
    BARRANGER, JA
    TAGER, JM
    SCHRAM, AW
    [J]. CLINICA CHIMICA ACTA, 1986, 158 (02) : 155 - 163
  • [2] AIRO R, 1993, HAEMATOLOGICA, V78, P129
  • [3] Allen MJ, 1997, QJM-MON J ASSOC PHYS, V90, P19
  • [4] AXELSSON U, 1966, ACTA MED SCAND, V179, P235
  • [5] Barak V, 1999, EUR CYTOKINE NETW, V10, P205
  • [6] INTERACTION BETWEEN A SERUM FACTOR AND LYMPHOCYTES-T IN GAUCHER DISEASE
    BASSAN, R
    MONTANELLI, A
    BARBUI, T
    [J]. AMERICAN JOURNAL OF HEMATOLOGY, 1985, 18 (04) : 381 - 384
  • [7] BENJAMIN D, 1979, SCAND J HAEMATOL, V22, P179
  • [8] METABOLISM OF GLUCOCEREBROSIDES .2. EVIDENCE OF AN ENZYMATIC DEFICIENCY IN GAUCHERS DISEASE
    BRADY, RO
    KANFER, JN
    SHAPIRO, D
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1965, 18 (02) : 221 - &
  • [9] BREIDENLANGEN CM, 1991, LEBER MAGEN DARM, V21, P126
  • [10] BREIDENLANGEN CM, 1991, LEBER MAGEN DARM, V21, P129