The February edition of the American Journal of Roentgenology was published earlier this week and there was a special focus on women’s imaging, in particular the issue of breast density and breast cancer risk. There were eight articles, including an editorial by Marcia Javitt of Haifa in Israel, as well as four reviews – on breast ultrasound, gamma imaging, breast density legislation, and magnetic resonance imaging – plus a clinical perspective on digital breast tomosynthesis, and an opinion piece on structured reporting for supplemental breast cancer screening. There was also an original research article on molecular breast imaging (MBI) used for supplementary screening in mammographically-dense breasts.
A group from the Mayo Clinic in Rochester, Minnesota, led by the physician Deborah Rhodes, has been trying for some years to encourage the use of MBI as a vital supplement to full-field digital mammography (FFDM). One of the main drawbacks of MBI is that it requires the intravenous injection of a contrast agent – the authors used Tc-99m sestamimbi – and this can add a radiation dose that is 10 to 20 times that of mammography. Rhodes’s team reduced the contrast agent dose by more than 50% and enrolled 1,585 women with either ‘dense’ or ‘very dense’ breasts in their study.
She also acknowledged there were circumstances when patients received too much radiation, but this was not the case for MBI: “Concern about a radiation level in the range of 2 mSv is not biologically warranted. If we tell patients that adding MBI to mammography doubles the dose of the exam, of course that doesn’t sound good. But if the goal is to find cancer, the test is important even if it means a higher but still safe amount of radiation.”
Among the important issues not addressed by Rhodes and her colleagues were the cost implications – both the MBI equipment and the contrast agent are expensive, with the latter applying to every patient screened.