Publication:
A randomized, intraindividual, non-inferiority, Phase III study comparing daylight photodynamic therapy with BF-200 ALA gel and MAL cream for the treatment of actinic keratosis.

dc.contributor.authorDirschka, T
dc.contributor.authorEkanayake-Bohlig, S
dc.contributor.authorDominicus, R
dc.contributor.authorAschoff, R
dc.contributor.authorHerrera-Ceballos, E
dc.contributor.authorBotella-Estrada, R
dc.contributor.authorHunfeld, A
dc.contributor.authorKremser, M
dc.contributor.authorSchmitz, B
dc.contributor.authorLübbert, H
dc.contributor.authorPuig, S
dc.date.accessioned2023-01-25T10:20:57Z
dc.date.available2023-01-25T10:20:57Z
dc.date.issued2018-08-14
dc.description.abstractThe most effective treatment modality for actinic keratosis (AK) is photodynamic therapy (PDT). Major obstacles of PDT are the need of a special illumination device and pain accompanying the illumination. These issues may be overcome by replacing an artificial high-power light source with natural daylight for more extended illumination at lower light doses. To determine whether BF-200 ALA (a nanoemulsion gel containing 7.8% 5-aminolaevulinic acid) is non-inferior to MAL (a cream containing 16% methyl-aminolaevulinate) in the treatment of mild-to-moderate AK with daylight PDT (dPDT). Non-inferiority of the primary efficacy variable (total lesion clearance rate per patient's side 12 weeks after PDT) is established if the mean response for BF-200 ALA is no worse than for MAL, within a statistical margin of Δ = -12.5%. The study was performed as an intraindividual comparison with 52 patients in seven centres in Germany and Spain. Each patient received one dPDT. Results include clinical endpoints as well as 1-year follow-up results. Twelve weeks after a single dPDT, 79.8% of the AK lesions treated with BF-200 ALA gel and 76.5% of the lesions treated with MAL cream were completely cleared. The median of differences was 0.0 with a one-sided 97.5% CI of 0.0, establishing non-inferiority (P Daylight PDT of AK with BF-200 ALA is well-tolerated and non-inferior to MAL/dPDT. The study demonstrates a trend towards higher efficacies after 3 months and significantly lower recurrence rates after 1 year follow-up.
dc.identifier.doi10.1111/jdv.15185
dc.identifier.essn1468-3083
dc.identifier.pmcPMC6585804
dc.identifier.pmid30022544
dc.identifier.pubmedURLhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6585804/pdf
dc.identifier.unpaywallURLhttps://onlinelibrary.wiley.com/doi/pdfdirect/10.1111/jdv.15185
dc.identifier.urihttp://hdl.handle.net/10668/12724
dc.issue.number2
dc.journal.titleJournal of the European Academy of Dermatology and Venereology : JEADV
dc.journal.titleabbreviationJ Eur Acad Dermatol Venereol
dc.language.isoen
dc.organizationHospital Universitario Virgen de la Victoria
dc.page.number288-297
dc.pubmedtypeClinical Trial, Phase III
dc.pubmedtypeComparative Study
dc.pubmedtypeJournal Article
dc.pubmedtypeMulticenter Study
dc.pubmedtypeRandomized Controlled Trial
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subject.meshAdministration, Cutaneous
dc.subject.meshAged
dc.subject.meshAminolevulinic Acid
dc.subject.meshFemale
dc.subject.meshGels
dc.subject.meshGermany
dc.subject.meshHumans
dc.subject.meshKeratosis, Actinic
dc.subject.meshMale
dc.subject.meshPhotochemotherapy
dc.subject.meshPhotosensitizing Agents
dc.subject.meshPrognosis
dc.subject.meshSeverity of Illness Index
dc.subject.meshSkin Cream
dc.subject.meshSpain
dc.subject.meshStatistics, Nonparametric
dc.subject.meshTreatment Outcome
dc.titleA randomized, intraindividual, non-inferiority, Phase III study comparing daylight photodynamic therapy with BF-200 ALA gel and MAL cream for the treatment of actinic keratosis.
dc.typeresearch article
dc.type.hasVersionVoR
dc.volume.number33
dspace.entity.typePublication

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