Photodynamic therapy with methyl aminolevulinate for prevention of new skin lesions in transplant recipients: A randomized study

被引:77
|
作者
Wennberg, Ann-Marie [1 ]
Stenquist, Bo [1 ]
Stockfleth, Eggert [2 ]
Keohane, Stephen [3 ]
Lear, John T. [4 ]
Jemec, Gregor [5 ]
Mork, Cato [6 ]
Christensen, Eidi [7 ]
Kapp, Alexander [8 ]
Solvsten, Henrik [9 ]
Talme, Toomas [10 ]
Berne, Berit [11 ]
Forschner, Tobias [2 ]
机构
[1] Gothenburg Univ, Sahlgrenska Univ Hosp, Dept Dermatol, SE-41345 Gothenburg, Sweden
[2] Univ Hosp Berlin, Charite, Dept Dermatol, Berlin, Germany
[3] St Marys Hosp, Dept Dermatol, Portsmouth PO3 GAD, Hants, England
[4] Manchester Royal Infirm, Dept Dermatol, Manchester M13 9WL, Lancs, England
[5] Roskilde Amtsygehus, Dept Dermatol, Roskilde, Denmark
[6] Univ Oslo, Rikshosp, Univ Hosp, Dept Dermatol, N-0027 Oslo, Norway
[7] St Olavs Hosp, Dept Dermatol, Trondheim, Norway
[8] Hannover Med Sch, Klin Dermatol & Allergol, Dept Dermatol, D-30623 Hannover, Germany
[9] Arhus Amtsygehus, Dermatovenerol Afdeling, Aarhus C, Denmark
[10] Karolinska Univ Hosp, Dept Dermatol, Stockholm, Sweden
[11] Univ Uppsala Hosp, Dept Dermatol, S-75185 Uppsala, Sweden
关键词
actinic keratosis; methyl aminolevulinate; photodynamic therapy; transplant recipients; prevention;
D O I
10.1097/TP.0b013e318180731e
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background. Organ transplant recipients on long-term immunosuppressive therapy are at increased risk of non-melanoma skin lesions. Repeated field photodynamic therapy using topical methyl aminolevulinate (MAL) may have potential as a preventive treatment. Methods. This open randomized, intrapatient, comparative, multicenter Study included 81 transplant recipients with 889 lesions (90% actinic keratoses (AK)]. In each patient, the study treatment was initially administered to one 50 cm(2) area on the face, scalp, neck, trunk, or extremities (n=476 lesions) twice (I week apart), with additional single treatments at 3, 9, and 15 months. On each occasion, the area was debrided gently and MAL cream (160 mg/g) applied for 3 hr, before illumination with noncoherent red light (630 mm, 37 J/cm(2)). The control, 50 cm(2) area (n=413 lesions) received lesion-specific treatment (83% cryotherapy) at baseline and 3, 9, and 15 months. Additionally, all visible lesions were given lesion-specific treatment 21 and 27 months in both treatment and control areas. Results. At 3 months, MAL photodynamic therapy significantly reduced the Occurrence of new lesions (65 vs. 103 lesions in the control area; P=0.01), mainly AK (46% reduction; 43 vs. 80; P=0.006). This effect was not significant at 27 months (253 vs. 312; P=0.06). Hypopigmentation, as assessed by the investigator, was less evident in the treatment than control areas (16% vs. 51% of patients; P<0.001) at 27 months. Conclusion. Our results suggest that repeated field photodynamic therapy using topical MAL may prevent new AK in transplant recipients although further studies are needed.
引用
收藏
页码:423 / 429
页数:7
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