Hereditary ovarian cancer in Poland
Article first published online: 1 JUL 2003
Copyright © 2003 Wiley-Liss, Inc.
International Journal of Cancer
Volume 106, Issue 6, pages 942–945, 10 October 2003
How to Cite
Menkiszak, J., Gronwald, J., Górski, B., Jakubowska, A., Huzarski, T., Byrski, T., Foszczyńska-Kłoda, M., Haus, O., Janiszewska, H., Perkowska, M., Brożek, I., Grzybowska, E., Zientek, H., Góźdź, S., Kozak-Klonowska, B., Urbański, K., Miturski, R., Kowalczyk, J., Plużańska, A., Niepsuj, S., Koc, J., Szwiec, M., Drosik, K., Mackiewicz, A., Lamperska, K., Stróżyk, E., Godlewski, D., Stawicka, M., Waśko, B., Bebenek, M., Rozmiarek, A., Rzepka-Górska, I., Narod, S. A. and Lubiński, J. (2003), Hereditary ovarian cancer in Poland. Int. J. Cancer, 106: 942–945. doi: 10.1002/ijc.11338
- Issue published online: 6 AUG 2003
- Article first published online: 1 JUL 2003
- Manuscript Accepted: 11 APR 2003
- Manuscript Revised: 21 FEB 2003
- Manuscript Received: 13 AUG 2002
- hereditary ovarian cancer;
There is increasing evidence that hereditary factors play a greater role in ovarian cancer than in any of the other common cancers of adulthood. This is attributable, to a large extent, to a high frequency of mutations in the BRCA1 or BRCA2 genes. In Poland, 3 common founder mutations in BRCA1 account for the majority of families with identified BRCA mutations. Our study was conducted in order to estimate the prevalence of any of 3 founder BRCA1 mutations (5382insC, C61G and 4153delA) in 364 unselected women with ovarian cancer, and among 177 women with ovarian cancer and a family history of breast or ovarian cancer. A mutation was identified in 49 out of 364 unselected women with ovarian cancer (13.5%) and in 58 of 177 women with familial ovarian cancer (32.8%). The majority of women with ovarian cancer and a BRCA1 mutation have no family history of breast or ovarian cancer. The high frequency of BRCA1 mutations in Polish women with ovarian cancer supports the recommendation that all Polish women with ovarian cancer should be offered testing for genetic susceptibility, and that counseling services be made available to them and to their relatives. It is important that mutation surveys be conducted in other countries prior to the introduction of national genetic screening programs. © 2003 Wiley-Liss, Inc.