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Protein could determine which tumors most likely to spread.  Appeared in CNN.
(AP) -- Measuring levels of a certain protein in a tumor could give
doctors an astonishingly accurate way of predicting whether early breast
cancer is likely to spread to the rest of a woman's body, a study
suggests.
If the preliminary findings hold up, doctors could someday use a growth
protein called cyclin E to tell which women need surgery plus chemotherapy
and which ones just need the tumor cut out.
Cyclin E appeared six times more powerful a predictor than the current
methods -- measuring tumor size and how far cancer cells have spread, said
biochemist Khandan Keyomarsi of the M.D. Anderson Cancer Center in
Houston.
In women with early-stage cancer that showed no sign of spreading, cyclin
E was 100 percent accurate in telling who would be alive six years later
and who would die within that time. It was more than 90 percent accurate
in those whose cancer had spread to the lymph nodes.
However, Keomarsi cautioned that the results might not be as impressive in
a bigger study.
Cyclin E "could potentially be very useful in helping to identify those
patients who may not need the grueling nature of chemotherapy, as well as
those who should be treated more aggressively," said Keyomarsi, whose
findings were reported in Thursday's New England Journal of Medicine.
Cyclin E is seen as a good marker, or predictor, because it plays a role
in cell growth, and cancer is essentially cell growth gone wild. Keyomarsi
said the protein could be the first reliable biological marker that can
distinguish between aggressive and non-aggressive breast cancer before it
spreads.
'Provocative' and intriguing
Other researchers described the research as intriguing, but they, too,
cautioned that it must be confirmed through additional studies and longer
follow-up of patients.
"It's very provocative, and I look forward to evolution of this particular
marker," said Dr. Larry Norton, head of solid tumor oncology and director
of the Breast Center at Memorial Sloan Kettering Cancer Center in New
York.
Keyomarsi said earlier, conflicting studies of cyclin E used antibodies to
find the protein. She instead employed a test that uses electric current
to separate proteins, and said it did better in head-to-head comparisons
against the antibody technique.
However, clinical laboratories generally do not have equipment for that
test. Moreover, breast tumor tissue is usually embedded in wax for
diagnosis, and the test that Khandan found to be superior needs fresh or
fresh-frozen tissue.
That could complicate efforts to develop a test for cycylin E, since fresh
tissue decays rapidly. Also, because mammograms are spotting cancer
earlier, many tumors are so small there is nothing left over for analysis
after the diagnosis, Norton said.
"If it turns out to be this useful as a prognostic factor, it would be
worth it," Norton said. "We'll have to wrestle with ways to accomplish
this."
A closer look at cyclin E
James Roberts, a scientist at the Fred Hutchinson Cancer Research Center
in Seattle, said researchers there did some early studies that suggested
cyclin E is a good marker for aggressive breast cancer. But he said more
standard markers of excessive cell growth may be just as good.
Keyomarsi's study looked at cyclin E levels in tissue from 395 women
diagnosed between 1990 and 1995.
A total of 114 of the women were diagnosed with early cancer that had not
yet spread. Twelve of them died, and all 12 had high levels of the
protein. The other women had low levels of the protein, and all of them
survived.
The difference was not quite as clear-cut for cancer in its later stages,
and there was no difference at all for cancer that had already spread past
the lymph nodes.
Generally, if cancer has not spread and the tumor is less than a
centimeter -- smaller than a fingernail -- doctors just remove it without
radiation or chemotherapy.

November 13, 2002.
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