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Familial and sporadic cases of nasopharyngeal carcinoma in Taiwan

  1. Author:
    Ung, A.
    Chen, C. J.
    Levine, P. H.
    Cheng, Y. J.
    Brinton, L. A.
    Chen, I. H.
    Goldstein, A. M.
    Hsu, M. M.
    Chhabra, S. K.
    Chen, J. Y.
    Apple, R. J.
    Yang, C. S.
    Hildesheim, A.
  2. Author Address

    Hildesheim A NCI, DCEG, Environm Epidemiol Branch, Interdisciplinary Studies Sect EPN 443 Bethesda, MD 20892 USA NCI, DCEG, Environm Epidemiol Branch, Interdisciplinary Studies Sect Bethesda, MD 20892 USA Howard Hughes Res Scholars Program Bethesda, MD 20814 USA Natl Taiwan Univ, Inst Epidemiol, Coll Publ Hlth Taipei Taiwan George Washington Univ, Sch Publ Hlth Washington, DC 20052 USA MacKay Mem Hosp, Dept Otolaryngol Taipei Taiwan Natl Taiwan Univ Hosp, Dept Otolaryngol Taipei Taiwan Natl Taiwan Univ, Coll Med, Inst Microbiol Taipei 10018 Taiwan NCI, Comparat Carcinogenesis Lab Frederick, MD 21702 USA Roche Mol Syst Alameda, CA USA
    1. Year: 1999
  1. Journal: Anticancer Research
    1. 19
    2. 1B
    3. Pages: 661-665
  2. Type of Article: Article
  1. Abstract:

    Background Nasopharyngeal carcinoma (NPC) has a striking geographic/ethnic distribution with especially high rates among southern Chinese. Previous studies have indicated that a family history of NPC is associated with increased risk and noted familial clustering in low-risk populations Materials and Methods: We investigated differences between sporadic and familial cases of NPC in a case-control study, of 375 histologically confirmed NPC cases (99% response late) and 328 age-, sex-, and geographically-matched controls (88% response rate). All participants answered a derailed risk factor interview and donated blood for EBV and CYP 2E1 testing Results: Subjects with a first degree relative with NPC had an odds ratio (OR) of 7.6 (95% confidence interval (CI) =2.3-25), while those with a family history of any other cancer had only a slightly elevated risk of disease (OR=1.4; 95% CI=.93-2.2). Of the cases, 25 (6.7%) were familial-having at least one first degree relative with NPC. No significant difference was seen between familial and sporadic cases with respect to sex, age, ethnicity, histology or stage. There was a nonsignificant (p =0.16) increase in TIN2 tumors among familial cases, suggesting a more aggressive tumor. Family history of other cancers, EBV serologies, or the distribution of the Rsal c2 form of the allele of cytochrome P450 2E1 were also not significantly different between the two groups. Conclusions: In conclusion, while genetic factors ale likely to play an important role in NPC pathogenesis, our results provide little evidence that a familial form of NPC exists with characteristics notably distinct from sporadic cases. [References: 21]

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