Red Light Photodynamic Therapy with 10% Aminolevulinic Acid Gel Showed Robust Efficacy for the Treatment of Superficial BCC in a Randomized, Vehicle-Controlled, Double-Blind, Multicenter Phase III Study

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Todd Schlesinger, MD, FAAD
M. Shane Chapman, MD, MBA
John H. Tu, MD, MS
Joel L. Cohen, MD
John Strasswimmer, MD, PhD, FAAD, FACMS
Nathalie C. Zeitouni, MD
Abel Torres, MD, JD, MBA
Sasha Jazayeri, MD
Mitchel P. Goldman, MD
Sherrif F. Ibrahim, MD, PhD
Edward L. Lain, MD, MBA
Megan P. Couvillion, MD, MS
Suzanne Bruce, MD
Vivian T. Laquer, MD
C. William Hanke, MD, MPH, FACP
David M. Ozog, MD
Jane Schneider, MD
Orit Markowitz, MD, FAAD
Brian Berman, MD, PhD
Mark S. Nestor, MD, PhD
Michael H. Gold, MD
Girish S. Munavalli, MD, MHS, FAAD, FACMS
Douglass W. Forsha, MD
Daniel M. Siegel, MD
David Mrohs, PhD
Beate Schmitz, PhD
Ruth Schäning, MSc
Nicole Pospiech, PhD
Jon Lyons, PhD, MBA
Montserrat Foguet, PhD
Matthias Lübbert, PhD
Hermann Lübbert, PhD
David M. Pariser, MD

Keywords

basal cell carcinoma (BCC), superficial basal cell carcinoma, red-light photodynamic therapy, ALA 10% gel

Abstract

Introduction: Basal cell carcinoma (BCC) is often treated surgically; however, depending on lesion size, location, or patient preference, surgery may not be the best option. Photodynamic therapy (PDT) has emerged as one alternative treatment for low-risk tumors like superficial BCC (sBCC). With this phase III study, we evaluated the efficacy and safety of red light PDT with 10% 5-aminolevulinic acid (ALA) gel versus vehicle in participants with sBCC.


Methods: This phase III, multicenter, randomized, double-blind, vehicle-controlled, parallel group study (NCT03573401) was conducted at 21 U.S. centers. Eligible participants had at least one naïve, histologically confirmed sBCC on the face, scalp, neck/trunk and/or extremities. One lesion per participant was defined as the main target lesion (MTL) for mandatory final excision. Additional lesions were treated but not excised. Either 10% ALA gel (BF-200 ALA, Ameluz®) or vehicle was applied to the lesions and incubated under occlusion for 3 to 3.5 hours, followed by illumination with BF-RhodoLED® (10 min, 635 nm, 37 J/cm²). Treatment was administered in PDT cycles (2 PDT sessions per cycle) with a maximum of 2 PDT cycles per participant. Clinical and histological assessments were performed 12 weeks after start of the last PDT cycle.


Results: Of the 187 randomized participants, 145 received 10% ALA gel and 42 received vehicle. Treatment with ALA gel resulted in significantly higher clearance rates compared with vehicle across all respective endpoints (p<0.0001 for all clearances). Clinical clearance of MTLs was achieved in 83.4% of patients in the ALA group versus 21.4% in the vehicle group. Histological clearance of MTLs was similarly superior with ALA gel (75.9% vs. 19.0%). Composite clearance of MTLs, defined as both clinical and histological clearance of MTLs, was observed in 65.5% of ALA-treated participants compared with only 4.8% in the vehicle group. Complete clinical clearance was achieved by 82.1% of participants treated with the ALA gel versus 21.4% of participants treated with vehicle. Combined clinical and histological clearance was achieved by 64.1% of participants in the ALA group versus 4.8% in vehicle. Overall clinical lesion clearance was also higher with ALA (82.6% vs. 21.6%). Esthetic outcomes were favorable in both groups but consistently better with ALA gel. Investigators rated 89.3% of ALA-treated lesions as having a very good or good cosmetic result, compared with 58.0% of vehicle-treated lesions. Participant-reported satisfaction was high regardless of treatment group, with 88.1% of lesions treated with ALA gel and 74.0% of vehicle-treated lesions rated as very good or good. No previously unknown adverse reaction occurred.


Conclusion: PDT with 10% ALA gel demonstrated significantly higher clearance rates versus vehicle, with favorable safety and aesthetic outcomes. These results support red light PDT with 10% ALA gel as a highly suitable non-surgical option for sBCC, particularly for multiple or large lesions, in low-risk areas, when patients either decline surgery or are not a good candidate for surgery.


The study was sponsored by Biofrontera Bioscience GmbH.

References

1. Morton et al., 2018: A randomized, multi-national, non-inferiority, phase III trial to evaluate the safety and efficacy of BF-200 ALA gel versus MAL cream in the treatment of non-aggressive basal cell carcinoma with photodynamic therapy (PDT). Br J Dermatol. doi:10.1111/bjd.16441

2. Chen et al., 2023: Photodynamic Therapy in Treating a Subset of Basal Cell Carcinoma: Strengths, Shortcomings, Comparisons with Surgical Modalities, and Potential Role as Adjunctive Therapy. Am J Clin Dermatol. doi:10.1007/s40257-023-00829-w

3. Al-Niaimi et al., 2015: Photodynamic Therapy Followed by Mohs Micrographic Surgery Compared to Mohs Micrographic Surgery Alone for the Treatment of Basal Cell Carcinoma: Results of a Pilot Single-Blinded Randomised Controlled Trial. J Cutan Aesthet Surg. doi:10.4103/0974-2077.158443 505

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