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dc.contributor.authorSalmivuori, M.
dc.contributor.authorGrönroos, M.
dc.contributor.authorTani, T.
dc.contributor.authorPölönen, I.
dc.contributor.authorRäsänen, J.
dc.contributor.authorAnnala, L.
dc.contributor.authorSnellman, E.
dc.contributor.authorNeittaanmäki, N.
dc.date.accessioned2020-03-25T09:15:11Z
dc.date.available2020-03-25T09:15:11Z
dc.date.issued2020
dc.identifier.citationSalmivuori, M., Grönroos, M., Tani, T., Pölönen, I., Räsänen, J., Annala, L., Snellman, E., & Neittaanmäki, N. (2020). Hexyl aminolevulinate, 5‐aminolevulinic acid nanoemulsion, and methyl aminolevulinate in photodynamic therapy of non‐aggressive basal cell carcinomas : A non‐sponsored, randomized, prospective and double‐blinded trial. <i>Journal of the European Academy of Dermatology and Venereology</i>, <i>34</i>(12), 2781-2788. <a href="https://doi.org/10.1111/jdv.16357" target="_blank">https://doi.org/10.1111/jdv.16357</a>
dc.identifier.otherCONVID_35099625
dc.identifier.urihttps://jyx.jyu.fi/handle/123456789/68317
dc.description.abstractBackground In the photodynamic therapy (PDT) of non‐aggressive basal cell carcinomas (BCCs), 5‐aminolevulinic acid nanoemulsion (BF‐200ALA) has shown non‐inferior efficacy when compared with methyl aminolevulinate (MAL), a widely used photosensitizer. Hexyl aminolevulinate (HAL) is an interesting alternative photosensitizer. To our knowledge, this is the first study using HAL‐PDT in the treatment of BCCs. Objectives To compare the histological clearance, tolerability (pain and post‐treatment reaction), and cosmetic outcome of MAL, BF‐200 ALA, and low‐concentration HAL in the PDT of non‐aggressive BCCs. Methods Ninety‐eight histologically verified non‐aggressive BCCs met the inclusion criteria, and 54 patients with 95 lesions completed the study. The lesions were randomized to receive LED‐PDT in two repeated treatments with MAL, BF‐200 ALA, or HAL. Efficacy was assessed both clinically and confirmed histologically at three months by blinded observers. Furthermore, cosmetic outcome, pain, post‐treatment reactions fluorescence, and photobleaching were evaluated. Results According to intention‐to‐treat analyses, the histologically confirmed lesion clearance was 93.8% (95% confidence interval [CI] = 79.9–98.3) for MAL, 90.9% (95% CI = 76.4–96.9) for BF‐200 ALA, and 87.9% (95% CI = 72.7–95.2) for HAL, with no differences between the arms (p=0.84). There were no differences between the arms as regards pain, post‐treatment reactions, or cosmetic outcome. Conclusions PDT with low‐concentration HAL and BF‐200 ALA have a similar efficacy, tolerability, and cosmetic outcome compared to MAL. HAL is an interesting new option in dermatological PDT, since good efficacy is achieved with a low concentration.en
dc.format.mimetypeapplication/pdf
dc.languageeng
dc.language.isoeng
dc.publisherWiley-Blackwell
dc.relation.ispartofseriesJournal of the European Academy of Dermatology and Venereology
dc.rightsIn Copyright
dc.subject.othernon‐aggressive basal cell carcinoma
dc.subject.otherphotodynamic therapy
dc.subject.othermethyl aminolevulinate
dc.subject.other5‐aminolevulinic acid nanoemulsion
dc.subject.otherhexyl aminolevulinate
dc.titleHexyl aminolevulinate, 5‐aminolevulinic acid nanoemulsion, and methyl aminolevulinate in photodynamic therapy of non‐aggressive basal cell carcinomas : A non‐sponsored, randomized, prospective and double‐blinded trial
dc.typearticle
dc.identifier.urnURN:NBN:fi:jyu-202003252534
dc.contributor.laitosInformaatioteknologian tiedekuntafi
dc.contributor.laitosFaculty of Information Technologyen
dc.contributor.oppiaineTietotekniikkafi
dc.contributor.oppiaineMathematical Information Technologyen
dc.type.urihttp://purl.org/eprint/type/JournalArticle
dc.type.coarhttp://purl.org/coar/resource_type/c_2df8fbb1
dc.description.reviewstatuspeerReviewed
dc.format.pagerange2781-2788
dc.relation.issn0926-9959
dc.relation.numberinseries12
dc.relation.volume34
dc.type.versionpublishedVersion
dc.rights.copyright© 2020 Wiley-Blackwell
dc.rights.accesslevelopenAccessfi
dc.subject.ysofotodynaaminen hoito
dc.subject.ysokarsinoomat
dc.format.contentfulltext
jyx.subject.urihttp://www.yso.fi/onto/yso/p2912
jyx.subject.urihttp://www.yso.fi/onto/yso/p28373
dc.rights.urlhttp://rightsstatements.org/page/InC/1.0/?language=en
dc.relation.doi10.1111/jdv.16357
jyx.fundinginformationThis clinical trial has been funded by research grants from the Finnish Dermatological Society, the Cancer Foundation Finland, the Foundation for Clinical Chemistry Research, the Instrumentarium Science Foundation, Tampere University, and the Competitive Research Financing of the Expert Responsibility Area of Tampere University Hospital.
dc.type.okmA1


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