Abstract
Interpretation
Multiplicative interaction of RT with mutation
status would be reflected by a larger association of RT with CBC among
carriers than among non-carriers, but this was not apparent.
Accordingly, there was no clear indication that carriers of deleterious
BRCA/
BRCA2
mutations were more susceptible to the carcinogenic effects of
radiation than non-carriers. These findings are reassuring and have
important clinical implications for treatment decisions and the clinical
management of patients harbouring deleterious
BRCA1/
BRCA2 mutations.
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