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Each year, some 20,000
people in the United States leave a doctor's office knowing they have a
primary brain tumor. More than half of those tumors are high-grade astrocytomas
that kill: That's the stark truth that powers brain cancer research in this
country. No small wonder, then, that Neurosurgeon in Chief Henry Brem, M.D.,
whose surgical practice gets worldwide referrals for brain tumors, says
clinical trials stand out as his profession's best hope. |
Brem
not only advocates trials in principle, but his own approaches often come
up for testing. At Hopkins, he reinstituted the Hunterian Neurosurgical
Research Laboratory, originally begun by Harvey Cushing. The chemotherapy-laced,
biodegradable wafer he helped develop and advance is the first FDA-approved
local therapy-it's implanted on the surgical surface-to help brain tumor
patients.
Brem's worked more than most to hasten therapy. In 1994, he and neuro-oncologist
Stuart Grossman, M.D., started New Approaches to Brain Tumor Therapy (NABTT),
an NIH-funded consortium of 11 top medical institutions that shares premier-quality
trials for drugs, immune therapy and other approaches. Now, Brem uses his
bully pulpit as head of Neurosurgery to advocate for trials.
Q.
Patients are wary of clinical trials. Sometimes their doctors are
as well. What could you say to convince them?
A. Start with the facts! Studies
show patients in trials do better than those who aren't. Cancer patients
in clinical studies have better outcomes, regardless of the treatment.
They live longer with a better quality of life.
Q.
Regardless of the treatment? Is that due to a placebo effect?
A. No, I think it's tied to human
nature. People enrolled in trials get a standard of care that's beyond
optimal. We believe our normal care is optimal. But because physicians
in trials know people are observing the data, the quality of what
they deliver is extremely high. Anybody does a bit more if the supervisor's
in the room.
Q. Do we have many brain tumor
trials ongoing?
A. Fifteen are still recruiting.
Some are Hopkins-initiated and approved by our institutional review
board. Others, like the NABTT studies, are part of larger, multicenter
projects.
Q. You said a quandary surrounds
the trials?
A. Yes. It can be difficult for
patients to decide whether to participate. Say a patient gets a standard
treatment drug. That patient may be excluded, then, from a trial of
a new systemic agent as an initial therapy. True, the standard offers
improved survival, but it's not a cure. So patient and physician must
decide whether known benefits outweigh potential promise of a new
treatment.
That creates a lot of tension in an institution! You find yourself
saying, "We have to do better for patients," but still, there's that
existing help, even though it's temporary.
Q. And most patients choose...
A. The treatment of known benefit.
But there is an out. If the tumor recurs, they can still try a trial
designed for recurring disease. That's why most new therapies first
appear for clinical failure rather than the initial approach.
Q. What keeps you able to face
patients with terminal tumors?
A. I alternate between two approaches.
First, I feel it's my obligation to see patients get the best possible
care, no matter what the probable outcome. That focuses my energy;
it gives me drive.
But if that's all I did, it would be depressing. So I'm also obligated
to try to improve their care through research. It gives hope, even
in a dismal disease, to me as well as to patients. In the long run,
it's the balance that keeps us all going. |
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