Evidence supports prognostic value
of circulating tumor cells in breast cancer
French researchers have reported the strongest proof
yet that evidence of 'circulating tumor cells' found in samples of a patient's
blood is strongly linked to poor outcomes such as a short time to disease progression.
At the IMPAKT Breast Cancer Conference in Brussels, Dr. Francois-Clement Bidard
and colleagues from Institut Curie in Paris say their new findings set the scene
for interventional trials designed to see if improved outcomes can be achieved
by modifying treatment based on circulating tumor cell counts.
"We needed to do this study to confirm data provided by earlier small
studies," Dr. Bidard said. "Now we are certain that circulating tumor
cells (CTC) are prognostic at baseline, and that CTC changes under treatment may
be an early indicator of chemotherapy efficiency."
"In metastatic breast cancer, it is time now for interventional randomized
trials which will try to demonstrate that CTC-based strategies of treatment lead
to a better clinical outcome, or at least to a benefit in the cost/efficacy ratio
of treatment," Dr. Bidard said.
The French team conducted a prospective study in 267 patients who were receiving
first-line chemotherapy for metastatic breast cancer. For each patient they performed
a count of circulating tumor cells, plus an analysis of other blood markers, in
7.5ml of blood. They took their measurements at the beginning of treatment and
at several later time points.
Of 260 patients who were evaluable for CTC levels at baseline, 170 (65%) had
at least one circulating tumor cell per 7.5 ml blood sample, and 115 (44%) had
five or more, the researchers found.
At the end of the study, a multivariate analysis of their results showed that
several factors, including CTC counts, were correlated with disease progression
and overall survival.
"This is the first study that has been prospectively designed and statistically
powered for reporting CTC-associated outcome as primary endpoint in a homogeneous
population of metastatic breast cancer patients treated first line," Dr.
Bidard said.
The study results also add evidence to an ongoing discussion about how many
CTCs per blood sample should be used to define patients at 'high risk' for a poor
outcome.
"Generally, the more CTC you have, the worse it is," Dr. Bidard said.
"However, to define a 'high risk group', a threshold is needed. We report
that the relative risk of the high-risk group vs low-risk group does not significantly
change whether you define it as having a threshold of 1 CTC or 5 CTC. In both
cases, their relative risks of shorter progression-free survival compared to the
low-risk group are statistically the same."
"Our data suggest that using the lower threshold of 1 CTC is feasible
and is not affected by any major loss of specificity of CTC detection. This supports
the use of this low threshold in other studies conducted in non-metastatic breast
cancer patients."
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