Risk reducing salpingectomy and delayed oophorectomy in high risk women: views of cancer geneticists, genetic counsellors and gynaecological oncologists in the UK

PENETRANCE Attitude of Health Personnel Ovariectomy BRCA High-risk FAMILIAL OVARIAN-CANCER 610 Risk reducing salpingectomy Genetic Counseling BREAST Salpingectomy 03 medical and health sciences 0302 clinical medicine RESPONSE RATES Ovarian cancer BRCA2 MUTATION CARRIERS Humans Genetic Predisposition to Disease Practice Patterns, Physicians' EARLY BILATERAL OOPHORECTOMY Germ-Line Mutation Genetics & Heredity BRCA2 Protein Ovarian Neoplasms Science & Technology BRCA1 Protein MORTALITY UNDERWENT OOPHORECTOMY Delayed oophorectomy Prognosis RRSDO 3. Good health FALLOPIAN-TUBE PROPHYLACTIC SALPINGECTOMY Oncology Female Life Sciences & Biomedicine Risk Reduction Behavior
DOI: 10.1007/s10689-015-9823-y Publication Date: 2015-07-15T09:55:37Z
ABSTRACT
Risk-reducing-salpingectomy and Delayed-Oophorectomy (RRSDO) is being proposed as a two-staged approach in place of RRSO to reduce the risks associated with premature menopause in high-risk women. We report on the acceptability/attitude of UK health professionals towards RRSDO. An anonymised web-based survey was sent to UK Cancer Genetics Group (CGG) and British Gynaecological Cancer Society (BGCS) members to assess attitudes towards RRSDO. Baseline characteristics were described using descriptive statistics. A Chi square test was used to compare categorical, Kendal-tau-b test for ordinal and Mann-Whitney test for continuous variables between two groups. 173/708 (24.4%) of invitees responded. 71% respondents (CGG = 57%/BGCS = 83%, p = 0.005) agreed with the tubal hypothesis for OC, 55% (CGG = 42%/BGCS = 66%, p = 0.003) had heard of RRSDO and 48% (CGG = 46%/BGCS = 50%) felt evidence was not currently strong enough for introduction into clinical practice. However, 60% respondents' (CGG = 48%/BGCS = 71%, p = 0.009) favoured offering RRSDO to high-risk women declining RRSO, 77% only supported RRSDO within a clinical trial (CGG = 78%/BGCS = 76%) and 81% (CGG = 76%/BGCS = 86%) advocated a UK-wide registry. Vasomotor symptoms (72%), impact on sexual function (63%), osteoporosis (59%), hormonal-therapy (55%) and subfertility (48%) related to premature menopause influenced their choice of RRSDO. Potential barriers to offering the two-stage procedure included lack of data on precise level of benefit (83%), increased surgical morbidity (79%), loss of breast cancer risk reduction associated with oophorectomy (68%), need for long-term follow-up (61%) and a proportion not undergoing DO (66%). There were variations in perception between BGCS/CGG members which are probably attributable to differences in clinical focus/expertise between these two groups. Despite concerns, there is reasonable support amongst UK clinicians to offering RRSDO to premenopausal high-risk women wishing to avoid RRSO, within a prospective clinical trial.
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