Surveillance of women at high risk for hereditary ovarian cancer is inefficient
- PMID: 16495917
- PMCID: PMC2361371
- DOI: 10.1038/sj.bjc.6603015
Surveillance of women at high risk for hereditary ovarian cancer is inefficient
Abstract
To determine the effectiveness of annual gynaecological screening (pelvic examination, transvaginal ultrasound, and CA-125), a prospective cohort study of women at high risk for hereditary ovarian cancer was conducted. Women were offered DNA analysis followed by either annual screening or prophylactic bilateral salpingo-oophorectomy (BSO). Study population consisted of 512 high-risk women (median follow-up 2.07 years, range 0-9.4 years): 265 women (52%) had a BRCA mutation. Persisting abnormalities indicated diagnostic surgery in 24 women resulting in one primary ovarian cancer FIGO stage IIIc was found. The effectiveness of screening was studied by calculating the probability of finding ovarian cancers in the BRCA-1 and BRCA-2 carrier group and comparing this to the identified number of ovarian cancers. The number of ovarian cancer patients found at surveillance was in accordance with the predicted number of ovarian cancers. A total number of 169 women underwent prophylactic BSO: one ovarian cancer stage IIb was found. In conclusion, the surveillance programme for hereditary ovarian cancer does identify patients with ovarian cancer but is very inefficient considering the high number of surveillance visits and the advanced stage of ovarian cancer in the identified patient. For prevention of advanced stage ovarian cancer, prophylactic BSO from age 35-40 years is a more efficient alternative.
Comment in
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Familial ovarian screening--effective or ineffective?Br J Cancer. 2006 Oct 23;95(8):1124; author reply 1126-7. doi: 10.1038/sj.bjc.6603407. Br J Cancer. 2006. PMID: 17047658 Free PMC article. No abstract available.
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High percentage of abnormal findings on TVU needs further discussion.Br J Cancer. 2006 Oct 23;95(8):1125; author reply 1126-7. doi: 10.1038/sj.bjc.6603408. Br J Cancer. 2006. PMID: 17047659 Free PMC article. No abstract available.
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