Psoriasis—systemic treatments


Research has confirmed psoriasis to be an immune-mediated inflammatory disease, with associated genes involved in immune regulation ( Fig. 18.1 ). These recent discoveries have allowed the pharmaceutical industry to specifically design biologic drugs that work in psoriasis and in other diseases where there is improved comprehension of the pathomechanisms. Biologics block specific inflammatory mediators or cells (see Chapter 61 ). Other systemic drugs are assumed to modify these mechanisms but their modes of action seem less well understood in comparison with the biologics.

Fig. 18.1
The molecular basis of psoriasis showing inflammatory changes from the initiating event to the acute lesion and on to the chronic plaque.
A vicious cycle of release of cytokines, chemokines and growth factors keeps the disease active. TNF-α is derived from Th1 cells and mediates inflammation by initiating a cascade of cytokines. IL-12 (derived from dendritic cells) and IL-23 are central to defining T-helper cell types and T-cell differentiation. The biologics break the cycle by negating the inflammatory action of TNF-α, IL-12 and other factors.

Non-biologic systemic therapy

Systemic treatment may be required for psoriasis that is:

  • Life-threatening, as in the erythrodermic or generalized pustular forms ( Fig. 18.2 )

    Fig. 18.2, Generalized pustular psoriasis.

  • Unresponsive to adequate topical treatment

  • So extensive that it is unlikely to respond to topical therapy (and fulfils Psoriasis Area Severity Index [PASI] and Dermatology Life Quality Index [DLQI] criteria for severity), as in widespread plaque psoriasis

  • Restricting the ability to work, as in acrodermatitis continua ( Fig 18.3 ).

    Fig. 18.3, Acrodermatitis continua variant of psoriasis.

Benefits must be weighed against side effects. The use of potentially toxic drugs is justified by their ability to transform a patient’s life from severely restricted to nearly normal. The type of psoriasis can influence the appropriateness of the treatment to be given. For example, palmoplantar psoriasis might respond well to acitretin ( Table 18.1 ). Phototherapy and photochemotherapy are outlined on page 134. Psoralen plus ultraviolet A (PUVA) is considered a systemic treatment as psoralen is taken by mouth.

Table 18.1
A guide to systemic therapy in psoriasis
Type of psoriasis Options for systemic treatment
Extensive plaque PUVA or Re-PUVA
Methotrexate, ciclosporin
Biologics
Palmoplantar Acitretin, PUVA or Re-PUVA
Generalized pustular Acitretin, methotrexate, ciclosporin
Biologics
Erythrodermic Acitretin, methotrexate, ciclosporin
Biologics

If the criteria to start systemic treatment are met, it is usual to consider the use of methotrexate first before proceeding to other systemic agents. This is provided there are no contraindications to methotrexate and no specific pointers to the use of an alternative as the first-line systemic drug.

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