LONDON--A multicenter clinical study has shown that a new noninvasive
diagnostic modality, which measures electropotentials at the skin
surface in the region of a suspicious breast lesion, helps physicians
discriminate benign lesions from breast cancer.
The device, developed by Biofield Corp., Atlanta, is similar to an
electrocardiogram in that measurements from the skin surface are made
with noninvasive sensors (figure).
Data suggest that rapidly proliferating cells, typical of cancer,
lose their normal charge or polarity, resulting in depolarization,
which can be measured by the devices sensors.
Researchers at eight European medical centers compared biopsy results
with Biofield test results in 661 women who underwent biopsy of a
suspicious breast lesion (Lancet 351:359-363, 1998). The test
provided highly significant predictive information only in women with
palpable lesions. Specificity was 55% with 90% sensitivity for women
with palpable lesions using an index based on electro-potential
differences and age.
"The lack of discrimination for nonpalpable lesions may be
related to difficulty with accurate sensor placement . . . based on
localization from mammograms," said Jack Cuzick, PhD, lead
author of the study and head of the Prevention and Control Section of
the Imperial Cancer Research Fund (ICRF).
Thus, the researchers concluded that the most promising use for the
new technique may be in women with lumps or inconclusive nodularity
detected on physical exam. "The prevalence of cancer in such
women is low, especially when they are young, and a simple test that
could reliably rule out malignant disease would help keep the number
of diagnostic tests done on these women to a minimum," Dr.
As a example, in a referral population with a 5% prevalence of
cancer, the Biofield test, operating with 90% sensitivity, would have
a negative predictive value of 99.1%, and would reduce the number of
women requiring additional tests by more than half.
The Biofield Diagnostic System will require pre-market approval (PMA)
from the FDA. It is scheduled to be available in Europe by late 1998.