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Clinical and Epidemiological Investigations

Cancer in Homozygotes and Heterozygotes of Ataxia-Telangiectasia and Xeroderma Pigmentosum in Britain

E. Clare Pippard, Andrew J. Hall, David J. P. Barker and Bryn A. Bridges
E. Clare Pippard
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Andrew J. Hall
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David J. P. Barker
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Bryn A. Bridges
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DOI:  Published May 1988
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Abstract

We have documented mortality and cancer incidence in the families of 67 patients with ataxia-telangiectasia and 48 patients with xeroderma pigmentosum resident in Britain. For both diseases, parents of patients are obligate heterozygotes and grandparents have a probability of heterozygosity of 0.5.

Fourteen ataxia-telangiectasia patients had died by June 30, 1986. This was a significant excess (14 deaths observed, 1.65 expected). Only one death was from a malignancy (non-Hodgkin's lymphoma). Three parents of ataxia-telangiectasia patients had died, all from cancer. The excess from breast cancer (two deaths observed, 0.17 expected) was statistically significant, p < 0.05. However, no excess mortality from malignant neoplasms was found in the grandparents.

Five xeroderma pigmentosum patients had died, none from internal malignancies. No excess mortality from malignant neoplasms was recorded in either their parents or grandparents.

Footnotes

  • ↵1 To whom requests for reprints should be addressed, at MRC Cell Mutation Unit, University of Sussex, Falmer, Brighton BN1 9RR, England.

  • Received August 12, 1987.
  • Revision received January 19, 1988.
  • Accepted February 8, 1988.
  • ©1988 American Association for Cancer Research.
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May 1988
Volume 48, Issue 10
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Cancer in Homozygotes and Heterozygotes of Ataxia-Telangiectasia and Xeroderma Pigmentosum in Britain
E. Clare Pippard, Andrew J. Hall, David J. P. Barker and Bryn A. Bridges
Cancer Res May 15 1988 (48) (10) 2929-2932;

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Cancer in Homozygotes and Heterozygotes of Ataxia-Telangiectasia and Xeroderma Pigmentosum in Britain
E. Clare Pippard, Andrew J. Hall, David J. P. Barker and Bryn A. Bridges
Cancer Res May 15 1988 (48) (10) 2929-2932;
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