Doctor Accused of Flawed Research
By TERRI LANGFORD Associated Press Writer

HOUSTON (AP) -- The research on a controversial cancer treatment is so
flawed that it cannot be determined whether it really works, three
prominent oncologists said.

"It is scientific nonsense," Dr. Howard Ozer, director of the
Allegheny Cancer Center in Philadelphia, said Wednesday.

Ozer and two other physicians examined Dr. Stanislaw Burzynski's
alternative cancer treatment known as antineoplastons for the Sept. 25
issue of The Cancer Letter, a widely read and well-respected
Washington newsletter.

Burzynski has claimed for years that antineoplastons, compounds found
in human urine and blood, "turn off" cancer genes by interrupting
signals that cause the cells to multiply. His treatment involves
giving synthetically made antineoplastons to patients orally or
intravenously.

Many among Burzynski's fiercely devoted clientele say they would be
dead without the therapy.

But the other doctors who reviewed Burzynski's data say his research
parameters are "poorly designed" and his data is "not interpretable."
Those factors may preclude the public from ever knowing whether his
treatment works, the researchers say.

In a faxed, nine-page response, Burzynski said his detractors'
findings can be attributed to their lack of complete information,
their lack of expertise, or the cancer suffered by the patient.

"The Cancer Letter, unfortunately, is not reporting the truth and only
truth," the statement said. "It is also reporting the lies of the
oncologists who were selected by The Cancer Letter to review the
annual report (submitted to the U.S. Food and Drug Administration)."

The three oncologists reviewed an annual report Burzynski submitted to
the FDA in an effort to obtain federal approval of his treatment. The
report included data Burzynski gathered from clinical trials of 963
patients who received antineoplastons over a 12-month period.

Statistics released in April and culled by the FDA from Burzynski's
preliminary reports show only 36, or 4.3 percent, of 828 patients
treated intravenously with antineoplastons responded positively to the
drug. Of the 36, 11 died.

Burzynski's lawyer, Rick Jaffe, claimed the FDA's totals were wrong
and he chided the agency for releasing preliminary data.

The other two physicians who evaluated the data were Peter Eisenberg,
a principal investigator with the Sutter Health West Cancer Research
Group, and Henry Friedman, chairman of the brain tumor committee of
the Pediatric Oncology Group.


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