Department of Dermatology and Allergy, University Hospital, LMU Munich, 80337, Munich, Germany.
Department of Dermatology, Center for Dermatooncology, University Hospital Tübingen, 72076, Tübingen, Germany.
Br J Dermatol. 2019 Jan;180(1):43-50. doi: 10.1111/bjd.17148. Epub 2018 Oct 31.
Actinic keratosis (AK) in organ transplant recipients (OTRs) has a high risk of progressing to invasive squamous cell carcinoma of the skin. Thus, early and consequent treatment of AKs is warranted in OTRs.
To summarize the current evidence for nonsystemic treatments of AKs in OTRs.
We performed a systematic literature search in MEDLINE, Embase and the Cochrane Central Register of Controlled Trials (CENTRAL) and hand-searched pertinent trial registers up to 22 August 2018. Randomized controlled trials (RCTs) evaluating nonsystemic interventions for AKs in OTRs were included. The risk of bias was estimated using the Cochrane Risk of Bias Tool.
Of 663 records initially identified, eight RCTs with 242 OTRs were included in a qualitative synthesis. Most studies evaluated methyl aminolaevulinate photodynamic therapy (MAL-PDT), followed by ablative fractional laser (AFXL) and diclofenac sodium 3% in hyaluronic acid, imiquimod 5% cream and 5-fluorouracil 5% cream (5-FU). MAL-PDT showed the highest rates of participant complete clearance (40-76·4%), followed by imiquimod (27·5-62·1%), diclofenac (41%) and 5-FU (11%). Similar results were observed for lesion-specific clearance rates. Treatment with AFXL alone revealed low lesion clearance (5-31%). Local skin reactions were most intense in participants treated with a combination of AFXL and daylight MAL-PDT. There were no therapy-related transplant rejections or worsening of graft function in any trial. The overall risk of bias was high.
Limited evidence is available for the treatment of AKs in OTRs. MAL-PDT is currently the best-studied intervention. Lesion-specific regimens may not be sufficient to achieve disease control. Field-directed regimens are preferable in this high-risk population.
光化性角化病(AK)在器官移植受者(OTR)中具有进展为皮肤侵袭性鳞状细胞癌的高风险。因此,OTR 中需要对 AK 进行早期和连续的治疗。
总结目前针对 OTR 中 AK 的非系统性治疗方法的证据。
我们对 MEDLINE、Embase 和 Cochrane 对照试验中央注册库(CENTRAL)进行了系统的文献检索,并在 2018 年 8 月 22 日之前对相关的试验登记册进行了手工搜索。纳入评估 OTR 中 AK 的非系统性干预措施的随机对照试验(RCT)。使用 Cochrane 偏倚风险工具评估偏倚风险。
最初确定的 663 条记录中,纳入了 8 项 RCT,共 242 名 OTR。大多数研究评估了甲氨基乙酰丙酸光动力疗法(MAL-PDT),其次是消融性点阵激光(AFXL)和双氯芬酸钠 3%在透明质酸、咪喹莫特 5%乳膏和 5-氟尿嘧啶 5%乳膏(5-FU)。MAL-PDT 显示参与者完全清除率最高(40-76.4%),其次是咪喹莫特(27.5-62.1%)、双氯芬酸钠(41%)和 5-FU(11%)。在特定病变的清除率方面也观察到了相似的结果。单独使用 AFXL 的治疗显示病变清除率较低(5-31%)。在接受 AFXL 和日光 MAL-PDT 联合治疗的参与者中,皮肤局部反应最为强烈。在任何试验中,都没有与治疗相关的移植排斥反应或移植物功能恶化。总体偏倚风险较高。
针对 OTR 中 AK 的治疗方法,证据有限。目前,MAL-PDT 是研究最多的干预措施。针对特定病变的治疗方案可能不足以控制疾病。在这种高风险人群中,针对病变区域的治疗方案更可取。