Module 13: Emerging Therapies and Current Guidelines in Dermatology
Learning Objectives
Section titled “Learning Objectives”By the end of this module, students should be able to:
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Describe the principles and indications of emerging therapies, including biologics and targeted small molecules, across common dermatological diseases.
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Summarize recent advances and current clinical guidelines for the management of key chronic dermatological conditions.
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Understand patient selection, monitoring requirements, and safety considerations for biologics and novel therapies.
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Apply knowledge of evolving therapies in clinical decision-making and evidence-based practice.
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Recognize the importance of multidisciplinary care and treatment guidelines in dermatology.
1. Introduction to Emerging Therapies in Dermatology
Section titled “1. Introduction to Emerging Therapies in Dermatology”-
Modern treatments focus on immune pathways and molecular targets in dermatologic diseases.
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Biologics: monoclonal antibodies targeting cytokines or cell surface markers.
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Small molecule inhibitors: oral agents targeting intracellular signalling pathways.
2. Biologics and Targeted Therapies: Applications and Mechanisms
Section titled “2. Biologics and Targeted Therapies: Applications and Mechanisms”Psoriasis and Psoriatic Arthritis
Section titled “Psoriasis and Psoriatic Arthritis”IL-17 and IL-23 inhibitors are preferred for biologic-naive patients with moderate-to-severe disease.
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Biologics targeting TNF-α (e.g., adalimumab, etanercept).
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IL-12/23 inhibitors (e.g., ustekinumab).
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IL-17 inhibitors (e.g., secukinumab, ixekizumab).
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IL-23 inhibitors (e.g., guselkumab, risankizumab).
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JAK inhibitors under investigation.
Atopic Dermatitis
Section titled “Atopic Dermatitis”Dupilumab is now recommended for moderate-to-severe cases unresponsive to topical therapy.
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Dupilumab: IL-4 receptor α antagonist blocking IL-4 and IL-13 signalling.
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Emerging agents: tralokinumab (anti-IL-13), JAK inhibitors (baricitinib, upadacitinib).
Hidradenitis Suppurativa
Section titled “Hidradenitis Suppurativa”- Biologics targeting TNF-α (adalimumab) with ongoing trials for IL-17 and IL-1 blockers.
Alopecia Areata
Section titled “Alopecia Areata”- JAK inhibitors (tofacitinib, ruxolitinib) are showing efficacy in hair regrowth.
3. Latest Clinical Guidelines Highlights (2024–2025)
Section titled “3. Latest Clinical Guidelines Highlights (2024–2025)”-
Psoriasis: Guidelines (e.g., American Academy of Dermatology [AAD], National Psoriasis Foundation) recommend biologics based on severity, comorbidities, and patient preference. Emphasize early intervention in moderate-to-severe disease. IL-17 and IL-23 inhibitors are preferred for biologic-naive patients with moderate-to-severe disease.
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Atopic Dermatitis: Updated consensus recommends dupilumab for moderate-to-severe AD not controlled with topical therapy. Systemic immunosuppressants for select cases.
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Skin Cancer: NCCN guidelines updated for melanoma immunotherapy, including checkpoint inhibitors (nivolumab, pembrolizumab).
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Monitoring: Guidelines stress screening for latent infections (TB, hepatitis), malignancy risk, and regular assessment of response and adverse effects when using biologics.
4. Safety and Monitoring
Section titled “4. Safety and Monitoring”-
Pre-treatment screening: TB (IGRA), hepatitis B/C, latent infections.
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Infection risk and immunization: Ensure vaccinations are up to date before initiating immunosuppressive therapy.
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Laboratory monitoring: Regular blood tests and patient education about signs of infection or adverse reactions.
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Multidisciplinary approach: Involving dermatologists, rheumatologists, and primary care.
5. Future Directions
Section titled “5. Future Directions”-
Personalized medicine approaches.
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Biomarkers guiding treatment choice and prognosis.
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Combination therapies and novel agents in clinical trials.
Multiple Choice Questions
Section titled “Multiple Choice Questions”Tap an answer to check yourself — the correct option and an explanation appear once you choose.
Q1 Which cytokine is the primary target of dupilumab in atopic dermatitis?
Dupilumab is an IL-4 receptor α antagonist that blocks both IL-4 and IL-13 signalling — the two key type 2 cytokines driving atopic dermatitis inflammation. TNF-α is targeted by adalimumab/etanercept (used in psoriasis and hidradenitis), IL-17 by secukinumab/ixekizumab (psoriasis), and IL-12 is part of the IL-12/23 axis targeted by ustekinumab.
Q2 Which biologic is approved for moderate-to-severe plaque psoriasis and targets IL-17?
Secukinumab is an IL-17 inhibitor approved for moderate-to-severe plaque psoriasis. Ustekinumab targets IL-12/23, adalimumab targets TNF-α, and dupilumab targets the IL-4 receptor α chain for atopic dermatitis.
Q3 Before starting a TNF-α inhibitor, which screening test is mandatory?
Screening for latent tuberculosis — using IGRA (interferon-gamma release assay) or chest X-ray — is mandatory before starting TNF-α inhibitors, as these agents can reactivate latent TB. While LFTs and renal function may also be checked, TB screening is the non-negotiable pre-treatment safety requirement stressed in current guidelines.
Short Answer Questions
Section titled “Short Answer Questions”SAQ 1: Indications for Biologic Therapy in Psoriasis
Section titled “SAQ 1: Indications for Biologic Therapy in Psoriasis”SAQ
List three indications for biologic therapy in patients with psoriasis.
Reveal model answer
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Moderate-to-severe plaque psoriasis not responding to topical or conventional systemic therapy.
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Psoriatic arthritis with active joint inflammation.
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Significant impact on quality of life or contraindications to traditional systemic agents.
SAQ 2: Safety Concerns with Biologic Therapies
Section titled “SAQ 2: Safety Concerns with Biologic Therapies”SAQ
Describe two common safety concerns with biologic therapies in dermatology.
Reveal model answer
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Increased infection risk, including reactivation of latent tuberculosis — hence the mandatory pre-treatment TB screening with IGRA or chest X-ray.
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Injection site reactions or hypersensitivity — patients should be educated to report local reactions; rare risks include malignancies or demyelinating diseases depending on the specific agent.
OSCE Station
Section titled “OSCE Station”OSCE 1: Counselling for Biologic Therapy in Psoriasis
Section titled “OSCE 1: Counselling for Biologic Therapy in Psoriasis”Scenario: A 34-year-old man with severe plaque psoriasis is referred for consideration of biologic therapy. You are tasked with counselling him during the clinic visit.
Task: Take a focused history including previous treatments and comorbidities, explain the role, benefits, risks, and monitoring of biologic therapy, and discuss the importance of screening tests before starting and ongoing follow-up.
Self-assess against checklist
Tick each point you covered, then check your score.
- Elicits treatment history: previous topical and systemic therapies tried, response, and reasons for escalation.
- Elicits disease impact on quality of life and any comorbidities (e.g., psoriatic arthritis).
- Explains in simple terms that biologics target specific immune pathways (cytokines) driving psoriasis.
- States that biologics can clear skin and control inflammation more effectively than prior treatments.
- Explains mandatory pre-treatment screening, specifically TB (IGRA or chest X-ray) and hepatitis B/C.
- Describes route of administration: subcutaneous injections given on a regular schedule.
- Informs about infection risk and advises patient to report signs of infection promptly.
- Mentions possible injection site reactions and rare adverse effects.
- Explains routine laboratory monitoring and follow-up schedule.
- Provides reassurance and invites patient questions.