9.3.2 Pharmacologic Basics of Systemic Therapy in Dermatology
Introduction
Systemic therapy is required in many dermatological, allergic, and venereal diseases when topical treatment is not sufficient. Use of systemic therapy has increased in the last decades, especially after introducing new agents in dermatological therapy (i.e. biologicals, small molecules). Before introducing therapy, it is mandatory to establish a correct diagnosis, evaluate potential contraindications, and consider possible side effects including drug interactions during the treatment.
Antibiotics
Antibiotics are used to treat infectious skin and venereal diseases and some other diseases due to their antimicrobial, anti-inflammatory, and immunomodulatory effects. In infectious diseases, antibiotics should be prescribed according to the infection type (typing of resistance pattern) and according to the spectrum of action. Antimicrobial resistance development should be avoided whenever possible (definite indication, avoid broad-spectrum antibiotics). Indications: primary (i.e., disseminated impetigo contagiosa, Lyme disease) and secondary (i.e., severely impetiginized eczema), deep bacterial infections of the skin as well as venereal diseases (i.e., syphilis, gonorrhoea), primarily non-infectious, but pathogen-associated diseases (i.e., severe acne), primarily non-pathogen-associated skin diseases (i.e., nodular rosacea).
Antihistamines
Antihistamines are competitive antagonists acting on the histamine receptor. In dermatology, most commonly used are H1 blockers as they are indicated for the treatment and the prophylaxis of allergic and pseudoallergic reactions. First-generation H1 blockers had sedative side-effects, which has been avoided in the second-generation antihistamines which do not cross the blood-brain barrier. Indications include urticaria, allergic rhinitis and conjunctivitis; intravenously administered antihistamines are the mainstay of the initial treatment of anaphylaxis.
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Antihistamines are competitive antagonists acting on the histamine receptor. In dermatology, most commonly used are H1 blockers as they are indicated for the treatment and the prophylaxis of allergic and pseudoallergic reactions. First-generation H1 blockers (e.g. diphenhydramine, hydroxyzine) have sedative side-effects, which have been avoided in the second-generation and new third generation antihistamines (e.g. cetirizine, loratadine, and fexofenadine/rupatadine and bilastine) that do not cross the blood-brain barrier. Indications include urticaria, allergic rhinitis and conjunctivitis; intravenously administered antihistamines are the mainstay of the initial treatment of anaphylaxis.
Antimycotics
Systemic antimycotics are used in the treatment of widespread or deep localised dermatomycoses as well as mycotic infections that affect hair and nails. Most commonly used groups of antimycotics are azole-type antifungals (i.e. fluconazole, itraconazole for the treatment of dermatophytes and yeasts) and allylamine derivates (i.e. terbinafine for the treatment of dermatophytoses). Griseofulvin is still used in the treatment of dermatophytoses.
Glucocorticoids
Glucocorticoids are the most widely used drugs in dermatology. Their main mode of action are anti-inflammatory, immunosuppressive and antiproliferative. Glucocorticosteroids are indicated in the therapy of inflammatory dermatoses, autoimmune dermatoses, granulomatous dermatoses, and other diseases that are not classified in one of these three groups. They are absolutely contraindicated in active untreated tuberculosis, systemic mycoses and ocular herpes simplex. The list of relative contraindications is much broader, including chronic gastritis, esophagitis and gastrointestinal bleeding, severe osteoporosis, glaucoma, depression etc. In those patients, glucocorticosteroids can be introduced if needed but with special prophylactic measures. Most common side effects are diabetes mellitus, hypertension, increased susceptibility to infections, osteoporosis, aseptic bone necrosis, gastrointestinal bleeding etc.
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Glucocorticoids are the most widely used drugs in dermatology. Their main mode of action are anti- inflammatory, immunosuppressive and antiproliferative. Glucocorticosteroids are indicated in the therapy of inflammatory dermatoses, autoimmune dermatoses, granulomatous dermatoses, and other diseases that are not classified in one of these three groups. They are absolutely contraindicated in active untreated tuberculosis, systemic mycoses and ocular herpes simplex. The list of relative contraindications is much broader, including chronic gastritis, esophagitis and gastrointestinal bleeding, severe osteoporosis, glaucoma, depression etc.; in these patients, glucocorticosteroids can be introduced if needed but with special prophylactic measures. The most common side effects are diabetes mellitus, hypertension, increased susceptibility to infections, osteoporosis, aseptic bone necrosis, gastrointestinal bleeding etc.
Common side effects of systemic glucocorticoids:
Hyperglycemia (diabetes);
Arterial hypertension (secondary);
Susceptibility to infections (e.g. herpes zoster);
Gastrointestinal bleeding and ulcers;
Osteopenia and osteoporosis;
Aseptic bone necrosis (e.g. aseptic femur head necrosis).
Retinoids
Retinoids include derivatives of vitamin A acid and substances with different chemical structures but related biological activities. They belong to the steroids superfamily.
Five groups of retinoids are available for the use in dermatology:
- acitretin
- alitretinoin
- bexarotene
- isotretinoin and
- tretinoin
The most common indications for use are psoriasis, palmoplantar hyperkeratosis, PRP (Pityriasis Rubra Pilaris), lichen planus for acitretin; refractory hand eczema for alitretinoin; cutaneous T-cell lymphomas for bexarotene; and severe and refractory forms of acne for isotretinoin. Contraindications: familial and clinically relevant acquired lipid metabolic disorders, simultaneous administration of tetracyclines, severe diabetes, pregnancy or plans to become pregnant and breastfeeding due to teratogenicity. Contraceptive care measures should be followed seriously.
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Retinoids include derivatives of vitamin A acid and substances with different chemical structures but related biological activities. They belong to the steroid superfamily.
Five groups of retinoids are available for the oral use in dermatology:
acitretin;
alitretinoin;
bexarotene;
isotretinoin;
tretinoin.
Most common indications for the use are psoriasis, palmoplantar hyperkeratosis, PRP (pityriasis rubra pilaris), lichen planus for acitretin; refractory hand eczema for alitretinoin; cutaneous T-cell lymphomas for bexarotene; and severe and refractory forms of acne for isotretinoin. Contraindications include familial and clinically relevant acquired lipid metabolic disorders, simultaneous administration of tetracyclines, severe diabetes, pregnancy or planning the pregnancy and breastfeeding due to the teratogenicity. Contraceptive care measures should be followed strictly. Most common side effects are cheilitis and xerosis cutis. Hair loss may occur during acitretin therapy. Increased transaminases and serum lipids are possible. Arthralgia, myalgia, headache and increased intracranial pressure are also on the list of side effects. Most side effects are dose dependent and reversible.
Antimetabolites
The two most important antimetabolites in systemic dermatological therapy are methotrexate and azathioprine. Methotrexate has a cytotoxic and immunomodulatory function. It is indicated in severe psoriasis, psoriatic arthritis, dermatomyositis, morphea, and some other dermatoses. It is usually prescribed once a week orally or subcutaneously. Contraindications for the therapy are pregnancy and lactation, acute infection, bone marrow depression and liver diseases. To avoid MTX overdose, folic acid should be given orally in parallel. Azathioprine is a cytotoxic agent used as an immunosuppressant. Main indications are autoimmune blistering diseases (in combination with glucocorticoids – as steroid-sparing agents). Other indications include vasculitis, lupus erythematosus, and pyoderma gangrenosum.
Antimalarials
Chloroquine and hydroxychloroquine are most commonly given in dermatology for the treatment of cutaneous and systemic lupus erythematosus. Glucose-6-phosphate dehydrogenase deficiency should be excluded before introducing therapy. Contraindication for introducing the drug is retinopathy, visual field restrictions, pregnancy and lactation. Ophthalmological consultations should be done before starting the treatment and in most patients after five years, in risk groups every year.
Dapsone
Dapsone is an antibacterial and anti-inflammatory drug, in dermatology most commonly used to treat dermatitis herpetiformis, linear IgA dermatosis and nodular vasculitis. Glucose-6-phosphate dehydrogenase deficiency should be excluded before introducing therapy. Methemoglobin should be checked regularly; hemolytic anaemia and agranulocytosis can occur.
Biologics and small molecules
Biologics are monoclonal antibodies which target specific proteins involved in the pathogenesis of various dermatological diseases, including psoriasis and metastatic melanoma.Small molecules are agents with a low molecular weight that can pass through cell membranes to modulate intracellular targets. They are most commonly used in the treatment of psoriasis and atopic dermatitis.
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Biologics are monoclonal antibodies which target specific proteins involved in the pathogenesis of various dermatological diseases, including psoriasis, psoriatic arthritis, metastatic melanoma, atopic dermatitis, hidradenitis suppurativa, pemphigus vulgaris, chronic urticaria, and cutaneous B-cell lymphomas. Biologics comprise tumor necrosis factor alpha (TNFα) inhibitors (adalimumab, infliximab, etanercept), interleukin (IL)-12/IL-23 inhibitors (ustekinumab), IL-17 inhibitors (secukinumab, ixekizumab, brodalumab), IL-4/IL-13 inhibitor (dupilumab, tralokimumab, baricitinib, upadacitinib), IL-1 antagonists (anakinra, canakinumab, rilonacept), CD20 inhibitor (rituximab). Most commonly used JAK inhibitors are baricitinib and upadacitinib.
TNFα inhibitors, IL-12/IL-23 inhibitors and IL-17 inhibitors are indicated in the treatment of psoriasis and psoriatic arthritis. Adalimumab is approved for the treatment of moderate and severe hidradenitis suppurativa, whereas other TNFα inhibitors (infliximab, etanercept) and anakinra are used off-label in this indication. Dupilumab and baricitinib are registered for the treatment of severe atopic eczema. Rituximab is indicated in the treatment of cutaneous B-cell lymphoma and pemphigus vulgaris. Omalizumab is an anti-IgE recombinant humanized monoclonal antibody that is indicated in the treatment of chronic spontaneous urticaria. In the treatment of advanced (non-resectable or metastatic) melanoma several biologics are approved, including ipilimumab (anti-cytotoxic T lymphocyte antigen-4 (anti-CTLA-4)) and PD-1 (programmed cell death protein-1) inhibitors nivolumab and pembrolizumab.
Small molecules (e.g. apremilast, an inhibitor of phosphodiesterase 4) are agents with a low molecular weight that can pass through cell membranes to modulate intracellular targets. They are most commonly used in the treatment of psoriatic arthritis and psoriasis. Small molecules are administered orally.
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