A phase I trial of aminolevulinic acid-photodynamic therapy for treatment of oral leukoplakia

التفاصيل البيبلوغرافية
العنوان: A phase I trial of aminolevulinic acid-photodynamic therapy for treatment of oral leukoplakia
المؤلفون: Bruce H. Campbell, Raymond C. Bergan, Ezra E.W. Cohen, Eva Szabo, Vamsi Parimi, Denis P. Lynch, Elizabeth M. Blair, Alexander Dew, Silvia Skripkauskas, Becky L. Massey, Borko Jovanovic, Stuart J. Wong, Peter Kulesza, Julia Shklovskaya, Rebecca M. Selle
المصدر: Oral Oncology. 49:970-976
بيانات النشر: Elsevier BV, 2013.
سنة النشر: 2013
مصطلحات موضوعية: Cancer Research, medicine.medical_specialty, medicine.medical_treatment, 030303 biophysics, Laser, Photodynamic therapy, Article, 03 medical and health sciences, Phase I, 0302 clinical medicine, stomatognathic system, Humans, Medicine, Photosensitizer, Leukoplakia, Biologic marker, 0303 health sciences, Photosensitizing Agents, business.industry, Aminolevulinic Acid, medicine.disease, Dermatology, 3. Good health, Light dose, Phase i study, Oral leukoplakia, stomatognathic diseases, Photochemotherapy, Oncology, 030220 oncology & carcinogenesis, Toxicity, Leukoplakia, Oral, Oral Surgery, business, therapeutics
الوصف: SummaryBackgroundPhotodynamic therapy with aminolevulinic acid (ALA PDT) for oral leukoplakia has shown promising effects in regression of oral leukoplakia. Although ALA has been extensively studied and is an ideal photosensitizer, the optimal light dose for treatment of oral leukoplakia has not been determined. We conducted a phase I study to determine MTD and DLT of PDT in patients treated with ALA for leukoplakia.MethodsPatients with histologically confirmed oral leukoplakia received a single treatment of ALA PDT in cohorts with escalating doses of light (585nm). Clinical, histologic, and biologic markers were assessed.ResultsAnalysis of 11 participants is reported. No significant toxicity from ALA PDT was observed in patients who received ALA with a light dose of up to 4J/cm2. One participant experienced transient grade 3 transaminase elevation due to ALA. One participant had a partial clinical response 3months after treatment. Biologic mucosal risk markers showed no significant associations. Determination of MTD could not be accomplished within a feasible timeframe for completion of the study.ConclusionsALA PDT could be safely administered with a light dose up to 4J/cm2 and demonstrated activity. Larger studies are needed to fully elucidate the MTD and efficacy of ALA-PDT.
تدمد: 1368-8375
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e9cde955467c2d25484070f2ec010863
https://doi.org/10.1016/j.oraloncology.2013.05.011
حقوق: OPEN
رقم الأكسشن: edsair.doi.dedup.....e9cde955467c2d25484070f2ec010863
قاعدة البيانات: OpenAIRE