At
Last, Silencing the Voices
(continued)
Says
Raymond: "She's come a long, long way. A lot of parents
would have just dropped her [at a treatment facility] off
and not done anything. But a lot of kids could go a lot further
if they're given the opportunity."
A
BITTER PILL. Robert Montalbano had tried plenty of
ways to cut his pack-a-day smoking habit over the past 15 years,
even trying hypnosis. But nothing worked. The Newark police
officer says he simply enjoys the taste of cigarettes too much.
"They were strong--filterless Camels," Montalbano
says, as he warmly recalls his smoking days.
But now Montalbano is confident he's stopped for good thanks
partly to a patent-pending lozenge that, when mixed with cigarette
smoke, creates a noxious metallic taste in the smoker's mouth.
"It's bitter, almost to the point of making you gag,"
says Montalbano.
The bitter pill was developed by Dr. Norman Hymowitz, a professor
of clinical psychiatry at the UMDNJ-New Jersey Medical School.
"Theoretically this works the same way that Antabuse therapy
would work for an alcoholic," says Dr. Hymowitz. "If
you take Antabuse and consume alcohol, you become sick. If people
are truly motivated to stop smoking, this lozenge could be effective
for them."
In a small pilot study with 50 smokers, including Montalbano,
about 40 percent were able to kick the habit using the lozenge--more
than twice the number who quit without it. The pill isn't available
commercially yet, and more studies are needed to determine how
effective the lozenge is in the long run. However, Dr. Hymowitz's
findings mimic short-term studies for similar products that
have been available in Europe for more than a decade.
The
European products--which are in the form of chewing gum--contain
about 6 milligrams of silver acetate, the substance that causes
the cherry-tasting tablets to become distasteful. Dr. Hymowitz's
tablet has only 2.5 milligrams of silver acetate. "We keep
it far below the FDA guidelines because there are limits to
how much silver acetate people can take without side effects,"
he says. "In lozenge form, the silver acetate lasts longer
and is just as effective in producing the aversive taste."
That metallic taste occurs when a person smokes within two hours
after consuming the tablet.
Patients
in the study took six tablets a day for three weeks, leading
up to the "quit day" they set for themselves. The
tablet isn't a cure-all; rather, it's part of an overall program
that includes recording every cigarette one smokes and pinpointing
concrete reasons to quit. "The lozenge helped get me off
cigarettes but I have a strong motivator for staying off--two
small children," says Montalbano. "They're so small--one's
eight and the other is four. I wouldn't want them to grow up
without a father."
Along with that powerful motivation, Montalbano keeps lozenges
in his car and his briefcase. "It's a strong reminder to
keep from faltering," says Montalbano. "If I ever
have the urge to smoke, I know I can pop one of these instead."
EARNING
WARNING.
A century ago, famed scientist Paul Ehrlich suggested that antibodies--proteins
produced by the immune system to ward off viruses and other
invaders--could be harnessed to pinpoint diseases. Somehow,
Ehrlich hypothesized, scientists would learn to use antibodies
as vehicles to carry cell-killing treatments directly to the
site of an illness.
Today,
his prediction is becoming reality. Scientists at the Princeton-based
Cytogen Corp. has discovered a way to use antibodies to diagnose
cancer, long before more traditional procedures could identify
the killing disease.
Their procedure uses monoclonal antibodies, proteins in the
immune system. These antibodies attach themselves to antigens,
microscopic features that jut out from viruses, disease-causing
bacteria, cancer cells and other substances that invade the
body. Cytogen's artificial antibodies, of course, bind to only
cancer sites.
The company's real breakthrough came when scientists discovered
a way to piggyback a tiny amount of low-dose radioactive material
to a monoclonal antibody without impeding the antibody's ability
to find a tumor. The monoclonal antibody is then injected intravenously
into the patient and, like a heat-seeking missile, binds to
a tumor sight. Within a few days, a device called a gamma camera
can take a "photography" of the body and determine
if any radioactive material has remained, meaning it has adhered
to a cancer cell.
The benefit of antibodies is their precision: An antibody will
stick to only one specific antigen. Diagnostic techniques now
used for cancer are much less precise. A computerized thermography
scan, for example, can be used to look at a specific "slice"
of the body and detect unusual masses in the tissues. But a
CT scan alone would not be able to differentiate a tumor from,
say, an abscess.
Because monoclonal antibodies bind only to diseased areas such
as cancerous cells, physicians say they can provide new information
that will affect treatment in 25 percent of cancer patients.
What's
more, monoclonal antibodies have great potential to detect cancerous
cells at an earlier stage. According to the American Cancer
Society, the 156,000 people who will develop colorectal cancer
have an 87 percent chance of surviving five years if their disease
is detected before it spreads to other parts of the body. "The
earlier we can diagnosis a cancer in a localized area, the more
options we have for treatment and the greater likelihood we'll
be successful," Dr. Gerald Murphy, chief medical officer
of the American Cancer Society in Atlanta. "Hopefully this
will pan out, and Cytogen has gone a long way to justifying
this hope."
Last year, seven European countries gave approval to Cytogen
products to detect ovarian cancer. This was the first time this
long-ballyhooed technology was given regulatory approval anywhere
in the world. In December, the FDA approved two Cytogen products
-- used to detect ovarian and colorectal cancer -- for use in
this country.
Cytogen is now going forward with the second phase of clinical
trials for monoclonal antibodies that would be used to fulfill
Ehrlich's dream of a "magic bullet": They deliver
therapeutic materials directly to a cancer site. [Note to Jenny:
While this development is interesting, it still is several years
of testing from application, so I wouldn't play it any higher.
Unlike chemotherapy, the cancer-killing substances would be
directed only to diseased tissue, rather than to the healthy
organ as well. "If we learn to target effectively, we could
avoid all the well-know side effects of chemotherapy, such as
nausea, hair loss, susceptibility to infections," says
Dr. Thomas McKearn, president of Cytogen Corp. "The treatment
wouldn't kill people anymore."
Like most new medical technology, the use of monoclonal antibodies
will be cautious. The first wave of curative products aren't
likely to appear before the end of the decade. However, Dr.
McKearn notes that this targeting technology could, some day,
be used to treat a host of debilitating conditions, such as
rheumatoid arthritis and Alzheimer's Disease.
"Cytogen
is a prototypical example of newer technology being moved from
the bench to the bedside," says Dr. Murphy of the American
Cancer Society. "I expect a lot of things from them. Cytogen
is an example of why we're so optimistic about cancer research
in general."
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