Advanced
Therapies Help Rheumatoid Arthritis
Combination therapies that include cutting-edge
steroids or the latest biologic agents are effective against early
stage rheumatoid arthritis (RA), according to a study reported in Arthritis
and Rheumatism.
The combined therapy appears to more rapidly and
effectively halt the crippling effects of early stage RA than conventional
single-drug therapies do, the researchers say.
"Initial treatment with a combination of drugs results
in an earlier regain of function, and less damage to the joints," says
study author Dr. Y.P.M. Goekoop-Ruiterman, of Leiden University Medical
Center in the Netherlands.
A chronic disease of the joints, RA often persists
throughout the lifetime of a diagnosed patient, potentially inflicting
long-term damage while causing extreme pain and a disabling loss of
mobility.
According to the Arthritis
Foundation (AF), more than 2 million Americans suffer from
RA, which usually first strikes between the ages of 30 and 50.
Although 70 percent of RA patients are women, men
are often seriously disabled by the disease.
Standard treatments have typically involved the
initial use of a single disease-modifying, anti-rheumatic drug (DMARD)
- perhaps later augmented with more DMARDs down the line.
Combination treatments involve the immediate multiple
use of DMARDs alongside other medications such as the steroid prednisone
or one of the newer biologic agents, such as infliximab (Remicade).
Biologic agents work by disabling the body's tumor
necrosis factor alpha (TNF) protein, which is known to promote inflammation.
To identify the best treatment, Dr. Goekoop-Ruiterman
and her colleagues offered the four most common treatment options to
508 early stage RA patients - mostly women - who lived in the Netherlands
when they were diagnosed with the disease between 2000 and 2002.
Divided equally into four groups, the patients were
all over the age of 18 and none had been diagnosed with the illness
for more than two years or treated with DMARD medications before the
study started.
The
first group started treatment with a so-called "conventional" DMARD
medication called methotrexate.
The
second group also took methotrexate, but as part of a "step-combination therapy" that
included the later addition of other DMARDs as well as prednisone.
The third group began a combination treatment that
immediately included methotrexate, the DMARD medication sulphasalazine,
and prednisone.
The
fourth group was given what was described as "the
most aggressive strategy" - methotrexate along with the TNF-blocking
infliximab.
The study provided functional ability exams, blood
tests, and X-rays of hand and feet joints.
These tests revealed that adverse side effects were
similar across all groups, and that nearly one-third of all the patients
had entered clinical remission from RA one year following the start
of treatment.
However, Dr. Goekoop-Ruiterman found that patients
included in the third and fourth treatment groups generally fared better
than those in the other groups.
After
one year, "low-disease activity" was observed
in 71 percent and 74 percent of the third and fourth groups, respectively.
This compared with 53 percent and 64 percent among the first and second
groups, respectively.
After three months of treatment, the researchers
found that functional and clinical improvements were occurring more
rapidly among the third and fourth groups - an outcome that held, to
a lesser degree, after a full year of treatment.
Also, more patients in the third and fourth groups
showed either less progression or no progression of joint disease after
one year than did patients who had been offered only one DMARD medication
to start.
Dr. Goekoop-Ruiterman concludes that, despite seemingly
better success with more aggressive therapies, the treatment-option
picture still remains cloudy.
She notes that starting with a single medication
option, such as methotrexate, did seem to adequately control RA for
more than 40 percent of the study patients.
This raised concerns that starting all patients
on more aggressive combination treatments might, in fact, lead to overtreatment.
However, the researcher also points out that the
faster relief of symptoms and physical function improvement among combination-therapy
patients were significant advantages of aggressive treatments.
This approach might help prevent long-term joint
damage by stopping the disease in its tracks at an earlier stage.
Dr. Stephen Lindsey, head of rheumatology at Ochsner
Clinic Foundation Hospital in New Orleans, says patients should be
evaluated on a case-by-case basis, for both medical and economic reasons.
"The trick is to establish which patients these
combination drugs are best for, because the newer biologic drugs cost
about $2,000 each month," he explains.
"So we need to tailor the more aggressive treatments
to the people who need it, and not forget about the standard treatments,
which many people do well on, which have less risk of infections because
there's less immunosuppression, and which are less expensive," notes
Dr. Lindsey.
Dr. Hayes Wilson, a rheumatologist and medical advisor
for the AF, agrees that money is always
an issue.
"In the real world, these biologic drugs are far
more expensive than DMARDs, and it's an economic reality that there
are patients who just can't afford it," comments Dr. Wilson. "Even
for insurance companies, a diagnosis of rheumatoid arthritis is like
a seven-alarm fire, because they know it's so expensive to treat."
Always consult your physician for more information.
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