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Many Patients with Advanced Cancers get
treatments that won't help
Newswise, June 9, 2011 — A study of more
than 1,000 patients with colon cancer that
had spread to distant sites found that one
in eight was treated with at least one drug
regimen that was not recommended. Those
patients were exposed to significant risk
without proven benefits, at an estimated
cost—just for the drugs—of more than $2
million.
The study, presented June 7, 2011, by
University of Chicago researchers at the
American Society for Clinical Oncology's
annual meeting in Chicago, focused on three
chemotherapy regimens that were not
supported by evidence from prior clinical
studies or clinical practice guidelines. One
treatment was rated "insufficient data to
support," one had been "shown to be
ineffective," and one was supported by "no
data, nor is there a compelling rationale."
"Patients with advanced cancers that do not
respond to standard therapies should either
be looking for clinical trials, where there
is a chance for a benefit, or should have
been thinking about shifting toward
palliative care," said study author Jonas De
Souza, M.D., a hematology/oncology fellow at
the University of Chicago.
"Patients should not face the risks,
discomforts and costs of aggressive and
often quite toxic chemotherapy with
treatment regimens that did not provide a
benefit in previous studies."
Under an agreement with United Healthcare, a
health benefits business, the researchers
used de-identified medical and
pharmaceutical claims data in the
collaborative project. They examined claims
from 7,642 colon cancer cases treated
between January 2007 and June 2010,
including 1,041 who developed metastatic
disease.
Of those 1,041 patients, 140 (13%) received
treatments that were not supported by the
evidence from clinical studies. Many of them
received multiple cycles of non-beneficial
chemotherapy.
The researchers focused on three
chemotherapy regimens with specific
recommendations against their use in the
National Comprehensive Cancer Network (NCCN)
guidelines. The regimen with insufficient
data involved bevacizumab (trade name
Avastin) used after the patient had
progressed on a combination of that drug and
chemotherapy. The treatment shown to be
"ineffective" was capecitabine (trade name
Xeloda) after progression on the same class
of drugs. The regimen with no compelling
rationale was panitumumab or cetuximab
(trade name Erbitux) after progression on
similar drugs.
The 140 patients received 869 cycles of
chemotherapy. Some received two or more
unproven treatments.
§
Ninety-one of those patients went through
632 intravenous cycles of bevacizumab, at an
estimated cost of $1.3 million. Potential
side effects include hypertension,
heightened risk of bleeding and bowel
perforation.
§
Fifty-nine patients received 218
non-evidence-based cycles of capecitabine,
at a cost of more than $600,000. This drug,
taken orally, can cause diarrhea, nausea,
vomiting, fatigue, rash and swelling of the
hands or feet.
§
Six patients underwent 19 cycles of
panitumumab, at a cost of almost $70,000.
This drug can trigger itching, dermatitis
and rash.
"We did not study why these physicians and
patients turned to unproven therapies," said
co-author Caleb Alexander, M.D., associate
professor of medicine at the University of
Chicago. "I suspect that both patients and
care providers, when facing life-threatening
disease with limited options, are more
willing to step outside guidelines."
"There could also be financial
implications," he added. "A physician who
has run out of options may be hesitant to
send a patient to a center that has access
to greater resources but may be far away."
The researchers emphasized, however, that as
the costs of cancer care continue to rise,
the impetus to base treatment decisions on
solid evidence can only increase. "It's
important to get the right medicines to the
right patients," said Alexander.
"DeSouza's research highlights the
importance of evidence-based treatment for
cancer patients," said Lee Newcomer, M.D.,
UnitedHealthcare's senior vice president,
oncology. "Expert oncology opinions tell us
that the extra therapies that these patients
received potentially exposed these patients
to unnecessary side effects. We should be
relieving symptoms and not causing new ones,
even as we try to address the underlying
disease."
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