Grenader Tal, Peretz Tamar, Lifchitz Meyer, Shavit Linda
Department of Oncology, Hadassah University Hospital, P.O. Box 12000, 91120 Jerusalem, Israel.
Breast. 2005 Aug;14(4):264-8. doi: 10.1016/j.breast.2005.01.005.
Approximately 10% of the cases of breast cancer and invasive ovarian cancer are hereditary, occurring predominantly in women with germ-line mutations in the BRCA1 or BRCA2 gene. In deciding whether women with germ-line mutations in the BRCA1 gene should use oral contraceptives a possible increase in the risk of breast cancer needs to be weighed against the convenience of this means of birth control and its potential to reduce the risk of ovarian cancer. In women with BRCA2 mutations, oral contraceptive use has not been associated with an increased risk of breast cancer and does have the potential to reduce the risk of ovarian cancer. Prophylactic surgical options and intensified surveillance should, of course, be discussed with these patients.
大约10%的乳腺癌和浸润性卵巢癌病例是遗传性的,主要发生在携带BRCA1或BRCA2基因种系突变的女性中。在决定携带BRCA1基因种系突变的女性是否应使用口服避孕药时,需要权衡乳腺癌风险可能增加与这种避孕方式的便利性及其降低卵巢癌风险的潜力。对于携带BRCA2突变的女性,使用口服避孕药与乳腺癌风险增加无关,且确实有可能降低卵巢癌风险。当然,应与这些患者讨论预防性手术选择和强化监测措施。