Knowledge Why is AFXL performed before PDT? Enhance Drug Delivery for Hypertrophic Actinic Keratosis Results
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Tech Team · Belislaser

Updated 2 days ago

Why is AFXL performed before PDT? Enhance Drug Delivery for Hypertrophic Actinic Keratosis Results


The primary reason for performing Ablative Fractional Laser (AFXL) before Photodynamic Therapy (PDT) is to physically breach the skin's protective barrier, a technique known as "laser-assisted drug delivery."

By utilizing lasers such as Carbon Dioxide (CO2) or Erbium (Er:YAG) to create microscopic vertical channels in the skin, clinicians can bypass the thickened, hyperkeratotic layer of the lesion. This pretreatment allows the photosensitizing drugs used in PDT to penetrate deeper and accumulate in higher concentrations, solving the absorption issues common in standard therapy.

Core Insight: Hypertrophic Actinic Keratosis features a thickened outer skin layer that blocks topical medication. AFXL pretreatment creates "micro-treatment zones" that bypass this barrier, significantly enhancing the depth and bioavailability of photosensitizers for superior clinical cure rates.

Overcoming the Barrier of Thickened Skin

The Limitation of Standard PDT

Standard Photodynamic Therapy relies on the passive absorption of a photosensitizer cream into the skin.

However, in hypertrophic (thickened) Actinic Keratosis, the outer layer of the skin—the stratum corneum—is excessively dense. This natural shield prevents the medication from reaching the deeper abnormal cells, often leading to incomplete treatment and lower cure rates.

Creating Micro-Treatment Zones

AFXL addresses this by using laser energy to ablate, or vaporize, tiny columns of tissue.

These microscopic vertical channels effectively drill through the hardened surface of the lesion. This process mechanically opens the skin without removing the entire surface layer, balancing aggressive treatment with safety.

Mechanisms of Enhanced Efficacy

Direct Delivery to the Junction

The micro-channels created by the laser act as direct conduits to the epidermal-dermal junction.

Instead of waiting for the drug to seep through layers of dead skin, the photosensitizer (such as ALA or MAL) is delivered directly into the active tissue. This bypasses the protective hyperkeratotic barrier that usually causes treatment failure.

Increased Bioavailability

Because the physical barrier is broken, the accumulation concentration of the drug within the lesion increases significantly.

This ensures that a higher percentage of abnormal cells absorb the photosensitizer. When the light activation phase of PDT follows, the reaction is more potent and creates a more thorough clearance of the lesion.

Reduced Incubation Time

Beyond efficacy, this technique offers a logistical advantage regarding treatment duration.

By bypassing the stratum corneum, the required "incubation time"—the wait between applying the drug and activating the light—can be reduced. Studies suggest a reduction from the traditional 3–4 hours down to 1.5–2 hours, improving clinical efficiency.

Understanding the Trade-offs

Increased Recovery Requirements

While AFXL-PDT is more effective, it is also more aggressive than PDT alone.

Because the laser physically ablates tissue, patients may experience distinct crusting and a slightly longer healing timeline compared to non-ablative methods. The "micro-wounds" require appropriate post-procedure care to prevent infection.

Pain Management Considerations

The combination of an ablative laser followed by chemical activation can be more uncomfortable than standard therapy.

The deeper penetration of the photosensitizer often results in a stronger phototoxic reaction during light exposure. Clinicians must often employ more robust pain management strategies during the procedure.

Making the Right Choice for Your Goal

When deciding on the integration of AFXL with PDT, consider the nature of the lesion and the patient's capacity for downtime.

  • If your primary focus is treating thick, resistant lesions: The addition of AFXL is essential to break the hyperkeratotic barrier and ensure the drug actually reaches the target cells.
  • If your primary focus is clinic efficiency: Utilizing AFXL can significantly reduce the required incubation time, allowing for faster patient turnover without sacrificing results.
  • If your primary focus is minimal downtime: You may need to weigh the superior cure rate of AFXL-PDT against the increased recovery time compared to standard, non-ablative therapies.

By physically opening the door to the dermis, AFXL transforms PDT from a surface-level treatment into a deep-acting therapy for resistant skin lesions.

Summary Table:

Feature Standard PDT AFXL-Pretreated PDT
Drug Delivery Passive absorption Laser-assisted deep delivery
Barrier Penetration Blocked by thick skin Bypasses hyperkeratotic layers
Incubation Time 3–4 Hours 1.5–2 Hours
Clinical Focus Superficial lesions Thick, resistant lesions
Healing Profile Minimal downtime Increased crusting/recovery
Cure Rates Lower for thick lesions Significantly higher

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  • Optimized ROI: Reduce patient incubation times and increase success rates for complex cases.

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References

  1. Katarzyna Małkińska, Dorota Krasowska. The use of photodynamic therapy in combined treatment of actinic keratosis. DOI: 10.5114/dr.2020.103889

This article is also based on technical information from Belislaser Knowledge Base .

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