Guidelines for follow-up of women at high risk for inherited breast cancer: Consensus statement from the Biomed 2 Demonstration Programme on Inherited Breast Cancer

Citation
P. Moller et al., Guidelines for follow-up of women at high risk for inherited breast cancer: Consensus statement from the Biomed 2 Demonstration Programme on Inherited Breast Cancer, DIS MARKER, 15(1-3), 1999, pp. 207-211
Citations number
24
Categorie Soggetti
Medical Research Diagnosis & Treatment
Journal title
DISEASE MARKERS
ISSN journal
02780240 → ACNP
Volume
15
Issue
1-3
Year of publication
1999
Pages
207 - 211
Database
ISI
SICI code
0278-0240(199910)15:1-3<207:GFFOWA>2.0.ZU;2-H
Abstract
Protocols for activity aiming at early diagnosis and treatment of inherited breast or breast-ovarian cancer have been reported. Available reports on o utcome of such programmes are; considered here. It is concluded that the on going activities should continue with minor modifications. Direct evidence of a survival benefit from breast and ovarian screening is not yet availabl e. On the basis of expert opinion and preliminary results from intervention programmes indicating good detection rates for early breast cancers and 5- year survival concordant with early diagnosis, we propose that women at hig h risk for inherited breast cancer be offered genetic counselling, educatio n in 'breast awareness' and annual mammography and clinical expert examinat ion from around 30 years of age. Mammography every second year may be suffi cient from 60 years on. BRCA1 mutation carriers may benefit from more frequ ent examinations and cancer risk may be reduced by oophorectomy before 40-5 0 years of age. We strongly advocate that all activities should be organize d as multicentre studies subjected to continuous evaluation to measure the effects of the interventions on long-term mortality, to match management op tions more precisely to individual risks and to prepare the ground for stud ies on chemoprevention.