Conclusions from 'Strategy to manage the treatment
of severe psoriasis: considerations
of efficacy, safety and cost'
Steven R Feldman, Rachel Garton, William Averett, Rajesh Balkrishnan &
Jeffrey Vallee: Departments of Dermatology, Pathology and Public Health Sciences, Wake Forest University School of
Medicine, Winston-Salem, NC 27157-1071, USA
Psoriasis is a common condition that has significant pharmacoeconomic
implications. Treatment with toxic or expensive
medications is often justified by the tremendous impact this
disease has on patients’ quality of life. The development of
new biological therapies adds considerably to the array of
options available to treat patients. While wonderfully effective
and relatively free of collateral organ toxicities, they are considerably
more costly compared to other established treatments.
These developments will bring pharmacoeconomic
considerations of psoriasis treatment to the forefront.
Expert opinion: First-line treatment for severe psoriasis
The use of UVB phototherapy is one of the least costly treatments
in terms of achieving treatment success and perhaps the
safest way to manage psoriasis. Unfortunately, it is inconvenient.
Given the cost and risks of alternative therapies, disincentives
to the use of office UVB phototherapy are not logical. Fair
reimbursement for the UVB procedure (at or above current
Medicare reimbursement levels) and elimination of patient copays
would encourage the use of this approach, improving
patient safety and reducing insurers’ exposure to high cost biological
therapies. Moreover, home UVB phototherapy should
be promoted for appropriate patients who require long-term
UVB as a maintenance therapy for their disease because this
would eliminate most of the major inconveniences of phototherapy:
frequent travel to the office for sessions, co-payments
for each treatment and lost time from work.
With its safety and efficacy, Goeckerman day treatment programmes
should also be encouraged as a first-line treatment
option for patients with severe psoriasis who would not be
expected to respond to UVB phototherapy alone. Encouraging
its use (i.e., providing appropriate reimbursement and eliminating
copays at each visit) would reduce the need for riskier
systemic therapies and for more costly biological treatments.
For patients who either do not respond or are not expected
to respond to UVB alone, the combination of UVB plus an
oral retinoid provides greater efficacy while maintaining an
excellent long-term safety profile. Phototherapy does not treat
psoriatic arthritis, so when significant arthritis is present, systemic
therapy will be needed.
Second-line treatment for severe psoriasis
Beyond the use of UVB, choosing the next step in psoriasis
management is complicated. Methotrexate offers a good efficacy:
cost ratio; however, short-term risks (haematological toxicity)
and long-term risks (hepatotoxicity) raise serious doubts
concerning its place as the second-line treatment for psoriasis.
PUVA is still a good consideration, with an excellent efficacy:
cost ratio but long-term risk of cutaneous malignancy
(including melanoma) makes its use as a standard second-line
agent less attractive.
From the standpoint of safety and efficacy, new biologicals
appear to be an excellent choice for patients who fail or are
not candidates for UVB phototherapy. The safety of alefacept
and the efficacy and good safety profile of TNF inhibitors
make these drugs promising as second-line agents from a
risk:benefit ratio standpoint. The higher cost of these theraStrategy
to manage the treatment of severe psoriasis: considerations of efficacy, safety and cost
8 Expert Opin. Pharmacother. (2003) 4(9)
pies, however, limits enthusiasm for a high position on the
therapeutic ladder.
In short, PUVA, methotrexate, alefacept and etanercept
(and probably infliximab and other TNF inhibitors) all
appear to be appropriate second-line choices for psoriasis,
each with advantages and disadvantages. Considerable patient
and physician judgement is required in deciding which of
these agents to prescribe in which order. Ideally, the cost-effectiveness
of therapies would be an important component of
this decision process. However, within a healthcare delivery
system in which payment is made by a third-party, patients
and physicians may have little or no incentive to consider the
cost of therapy. Developing an acceptable approach to encouraging
such consideration is problematic. The cost of biological
therapy is so great that even a 10 – 20% copay for such a
therapy might put the therapy out of reach of patients who
need it for control of their disease.
Different structures of healthcare financing provide very
different incentives for choice of therapies. Patients who have
first dollar coverage for drug costs may be inclined to choose
etanercept over other options, including phototherapy.
Patients without prescription drug coverage have an incentive
to choose physician-delivered treatments, such as alefacept,
that would likely fall under their medical benefit.
Third-line treatment for severe psoriasis
The long-term risk of nephrotoxicity in cyclosporin therapy
precludes recommending it for the long-term management of
psoriasis above other, less toxic alternatives. Its higher cost
compared to other, non-biological psoriasis therapies also limits
enthusiasm for its use. However, it is still an appropriate
therapy for short-term treatment of a disease flare, for reducing
disease severity before transitioning to a safer long-term
treatment or for patients not adequately controlled with other
treatments. Hydroxyurea because of its very narrow therapeutic
window, is another third-line agent for the management of
severe psoriasis.
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