ASSESSMENT OF RELATIVE RISK OF 2ND PRIMARY TUMORS AFTER OVARIAN-CANCER AND OF THE USEFULNESS OF DOUBLE PRIMARY CASES AS A SOURCE OF MATERIAL FOR GENETIC-STUDIES WITH A CANCER REGISTRY
S. Shah et al., ASSESSMENT OF RELATIVE RISK OF 2ND PRIMARY TUMORS AFTER OVARIAN-CANCER AND OF THE USEFULNESS OF DOUBLE PRIMARY CASES AS A SOURCE OF MATERIAL FOR GENETIC-STUDIES WITH A CANCER REGISTRY, Cancer, 72(3), 1993, pp. 819-827
Background. It now is accepted that a small proportion of people with
certain forms of cancer have a dominantly inherited gene fault that pr
edisposes them to it. This is more likely with an early age at onset o
r when the person has had multiple primary tumors. Methods. Population
-based data from the North West Regional Cancer Registry of England re
garding 4157 ovarian cancer cases diagnosed between 1980 and 1989 were
analyzed to determine the relative risks (RR) of second primary breas
t and colorectal carcinomas. Results. Elevated risks approaching signi
ficance were observed for breast and colorectal carcinoma subsequent t
o ovarian cancer. After stratification into groups for ovarian histopa
thologic characteristics and age at onset, significantly elevated risk
s were obtained for both breast and colorectal tumors after ovarian ca
rcinoma for women younger than 60 years of age at onset and with serou
s histopathologic characteristics (breast RR, 2.68, P < 0.05; colorect
al RR, 4.25, P < 0.05). Conclusions. These results emphasize the need
for greater awareness of the possibility of development of additional
cancer after ovarian carcinoma in high-risk groups. Overall, the study
supports the theory that breast, colorectal, and ovarian tumors are r
elated genetically.