scholarly journals LB941 Photodynamic therapy (PDT) with aminolevulinic acid (ALA) 20% and blue light reduces occurrence of actinic keratoses (AK) and de novo non-melanoma skin cancers (NMSCs) in patients with field cancerization

2017 ◽  
Vol 137 (10) ◽  
pp. B2 ◽  
Author(s):  
S. Marcus ◽  
D. Piacquadio ◽  
A. Houlihan ◽  
M. Ferdon ◽  
J. Berg
1998 ◽  
Vol 16 ◽  
pp. S208
Author(s):  
Edward Jeffes ◽  
Jerry McCullough ◽  
Gerald Weinstein ◽  
Toni Shull ◽  
Ross Kaplan ◽  
...  

2004 ◽  
Vol 140 (1) ◽  
Author(s):  
Daniel J. Piacquadio ◽  
Diana M. Chen ◽  
Harold F. Farber ◽  
Joseph F. Fowler, Jr ◽  
Scott D. Glazer ◽  
...  

2004 ◽  
Vol 8 (2) ◽  
pp. 131-139 ◽  
Author(s):  
Younan Liu ◽  
Gilles Viau ◽  
Robert Bissonnette

Background: The use of photodynamic therapy (PDT) with topical aminolevulinic acid (ALA) on large skin surfaces has recently been reported for patients with multiple actinic keratoses. Objective: The current study compared the ability of topical and systemic ALA–PDT as well as topical ALA–PDT with blue light to delay the appearance of UV-induced skin cancer using the hairless mouse as a model. Methods: Groups of hairless mice were exposed daily to UV radiation and weekly to ALA–PDT. Tumor-free survival was compared for mice exposed to UV and treated weekly with ALA–PDT and mice exposed only to UV radiation. Results: Weekly topical or systemic ALA–PDT was able to delay the induction of skin tumors. A significant difference in tumor-free survival was also observed for both actinic keratoses and invasive squamous cell carcinoma in mice treated weekly with topical ALA–PDT performed with blue light. This was observed even when weekly ALA–PDT was started after 8 weeks of UV exposure. Conclusion: Large-surface topical ALA–PDT with blue light can delay the appearance of UV-induced actinic keratoses and squamous cell carcinoma in hairless mice.


2001 ◽  
Vol 45 (1) ◽  
pp. 96-104 ◽  
Author(s):  
Edward W. Jeffes ◽  
Jerry L. McCullough ◽  
Gerald D. Weinstein ◽  
Ross Kaplan ◽  
Scott D. Glazer ◽  
...  

2013 ◽  
Vol 2013 ◽  
pp. 1-7 ◽  
Author(s):  
Christina Wlodek ◽  
Faisal R. Ali ◽  
John T. Lear

Solid organ transplant recipients are predisposed to actinic keratoses (AK) and nonmelanoma skin cancers, owing to the lifelong immunosuppression required. Today, increasing numbers of organ transplants are being performed and organ transplant recipients (OTRs) are surviving much longer. Photodynamic therapy (PDT) is proving a highly effective treatment modality for AK amongst this susceptible group of patients. Following an overview of the pathogenesis of AK amongst OTRs, the authors review current safety and efficacy data and how this relates to the role of PDT for the treatment of AK in OTRs.


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