Bulletin du Cancer
Summary : The aim of this survey of practice was to define, in
the absence of guideline, the management in France of asymptomatic men
bearing a mutation of
BRCA1 or
2 genes. A questionnaire was addressed to 90 oncogenetics
centers. We obtained the answers of 34 practitioners working in
58 centers. Among the responders, 85.3% offered a systematic genetic
test in all cases to determine the risk of transmission to the children
and to offer a personal follow-up in 79.4 % of cases. This screening was
directed towards prostate cancer, breast cancer and pancreatic cancer
in respectively 94.1, 67.6 and 47.1% of cases. The screening of prostate
cancer was mainly proposed to men bearing a BRCA2 mutation and from the
age of 40 years. It was based on clinical examination and testing of
prostate specific antigen. The screening of breast cancer was mainly
proposed to men bearing a BRCA2 mutation and based on clinical
examination and self-palpation without stating a started age. The
screening of pancreatic cancer was mainly proposed to men with familial
history of pancreatic cancer and from the age of 40 years. It was based
on tomography and MRI. For the majority of answerers, the general
practitioner was the best to perform all these screenings. These
experts’ opinions can help to establish guidelines for the global
management of asymptomatic men carriers of BRCA1 or 2 mutations.
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