This AP article is such patent by-the-book allopathic/FDA propaganda that
it is laughable.  The  FDA picks medical atavists to "review" the work of
their natural enemy--i.e., anyone with a new paradigm that threatens their
economic security.  Stephanie Dallam, I can't believe that anyone who
subscribes to these lists can be this uninformed.  Therefore I ask, Who is
your owner???

Vincent Gammill

----------
> From: Stephanie Dallam <[email protected]>
> To: [email protected]; [email protected]
> Subject: CS>Burzynski Accused of Flawed Research
> Date: Thursday, October 01, 1998 9:05 AM
> 
> 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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