Journal of Clinical Oncology, Vol 12, 1724-1736, Copyright © 1994 by American Society of Clinical Oncology
Quantitating familial cancer risk: a resource for clinical oncologists
K Offit and K Brown
Department of Human Genetics, Memorial Sloan-Kettering Cancer Center, New York, NY.
PURPOSE: Because a family history of cancer constitutes an important risk
factor, estimation and communication of cancer risk can facilitate efforts
toward early detection and prevention. This review provides a resource for
health professionals called to draw upon a multidisciplinary literature to
provide quantitative risk estimates to families with cancer. DESIGN:
Descriptive population-derived, epidemiologic, genetic, genetic
epidemiologic, and molecular studies are critically reviewed in the context
of cancer genetic counseling. RESULTS: Data are presented that document the
increased lifetime relative risk to relatives of individuals with cancers
of the breast, ovary, colon, prostate, or other sites. In general, risk
ratios are poorly suited for clinical counseling. Age-specific absolute
risks are presented for first-degree relatives of individuals affected by
cancers of the breast, ovary, and colon. The derivation of Mendelian and
Bayesian risk estimates in the setting of well-defined cancer family
syndromes, and the growing role of DNA testing in more accurately assessing
these risks, are discussed. Such carrier testing requires careful
psychologic and ethical considerations. CONCLUSION: Multidisciplinary
cancer genetic counseling is an emerging resource available to physicians
who care for families with common adult malignancies.

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