Bae Jung Min, Jung Han Mi, Hong Bo Young, Lee Joo Hee, Choi Won Joon, Lee Ji Hae, Kim Gyong Moon
Department of Dermatology, St Vincent's Hospital, College of Medicine, The Catholic University of Korea, Suwon, Korea.
Department of Rehabilitation Medicine, St Vincent's Hospital, College of Medicine, The Catholic University of Korea, Suwon, Korea.
JAMA Dermatol. 2017 Jul 1;153(7):666-674. doi: 10.1001/jamadermatol.2017.0002.
References to the expected treatment response to phototherapy would be helpful in the management of vitiligo because phototherapy requires long treatment durations over several months.
To estimate the treatment response of vitiligo to phototherapy.
A comprehensive database search of MEDLINE, EMBASE, and the Cochrane library from inception to January 26, 2016, was performed for all prospective studies. The main keywords used were vitiligo, phototherapy, psoralen, PUVA, ultraviolet, NBUVB, and narrowband.
All prospective studies reporting phototherapy outcome for at least 10 participants with generalized vitiligo were included. Of 319 studies initially identified, the full texts of 141 studies were assessed for eligibility, and 35 were finally included in the analysis. Of these, 29 studies included 1201 patients undergoing narrowband UV-B (NBUVB) phototherapy, and 9 included 227 patients undergoing psoralen-UV-A (PUVA) phototherapy.
Two reviewers independently extracted the following data: study design, number and characteristics of the participants, phototherapy protocol, and rate of repigmentation based on the quartile scale. Single-arm meta-analyses were performed for the NBUVB and PUVA groups. Sample size-weighted means were calculated using a random-effects model for the repigmentation rates of the included studies.
The primary outcomes were at least mild (≥25%), at least moderate (≥50%), and marked (≥75%) responses on a quartile scale. Response rates were calculated as the number of participants who showed the corresponding repigmentation divided by the number of all participants enrolled in the individual studies.
The meta-analysis included 35 unique studies (1428 unique patients). For NBUVB phototherapy, an at least mild response occurred in 62.1% (95% CI, 46.9%-77.3%) of 130 patients in 3 studies at 3 months, 74.2% (95% CI, 68.5%-79.8%) of 232 patients in 11 studies at 6 months, and 75.0% (95% CI, 60.9%-89.2%) of 512 patients in 8 studies at 12 months. A marked response was achieved in 13.0% (95% CI, 2.1%-23.9%) of 106 patients in 2 studies at 3 months, 19.2% (95% CI, 11.4%-27.0%) of 266 patients in 13 studies at 6 months, and 35.7% (95% CI, 21.5%-49.9%) of 540 patients in 9 studies at 12 months. For PUVA phototherapy, an at least mild response occurred in 51.4% (95% CI, 28.1%-74.7%) of 103 patients in 4 studies at 6 months and 61.6% (95% CI, 20.2%-100%) of 72 patients in 3 studies at 12 months. In the subgroup analyses, marked responses were achieved on the face and neck in 44.2% (95% CI, 24.2%-64.2%), on the trunk in 26.1% (95% CI, 8.7%-43.5%), on the extremities in 17.3% (95% CI, 8.2%-26.5%), and on the hands and feet in none after at least 6 months of NBUVB phototherapy.
Long-duration phototherapy should be encouraged to enhance the treatment response in vitiligo. The greatest response is anticipated on the face and neck.
由于光疗需要持续数月的长时间治疗,因此提及光疗的预期治疗反应将有助于白癜风的管理。
评估白癜风对光疗的治疗反应。
对MEDLINE、EMBASE和Cochrane图书馆从创刊至2016年1月26日进行全面数据库检索,以查找所有前瞻性研究。使用的主要关键词为白癜风、光疗、补骨脂素、PUVA、紫外线、NBUVB和窄带。
纳入所有报告至少10名泛发性白癜风患者光疗结果的前瞻性研究。在最初确定的319项研究中,对141项研究的全文进行了资格评估,最终35项纳入分析。其中,29项研究纳入了1201例接受窄谱中波紫外线(NBUVB)光疗的患者,9项研究纳入了227例接受补骨脂素-长波紫外线(PUVA)光疗的患者。
两名研究者独立提取以下数据:研究设计、参与者数量和特征、光疗方案以及基于四分位数量表的色素再生率。对NBUVB和PUVA组进行单臂荟萃分析。使用随机效应模型计算纳入研究色素再生率的样本量加权均值。
主要结局为在四分位数量表上至少有轻度(≥25%)、至少有中度(≥50%)和显著(≥75%)反应。反应率计算为显示相应色素再生的参与者数量除以各研究中纳入的所有参与者数量。
荟萃分析纳入35项独特研究(1428例独特患者)。对于NBUVB光疗,3项研究中130例患者在3个月时至少有轻度反应的发生率为62.1%(95%CI,46.9%-77.3%),11项研究中232例患者在6个月时为74.2%(95%CI,68.5%-79.8%),8项研究中51,2例患者在12个月时为75.0%(95%CI,60.9%-89.2%)。2项研究中106例患者在3个月时显著反应的发生率为13.0%(95%CI,2.1%-23.9%),13项研究中266例患者在6个月时为19.2%(95%CI,11.4%-27.0%),9项研究中540例患者在12个月时为,35.7%(95%CI,21.5%-49.9%)。对于PUVA光疗,4项研究中103例患者在6个月时至少有轻度反应的发生率为51.4%(95%CI,28.1%-74.7%),3项研究中72例患者在12个月时为61.6%(95%CI,20.2%-100%)。在亚组分析中,NBUVB光疗至少6个月后,面部和颈部显著反应的发生率为44.2%(95%CI,24.2%-64.2%),躯干为26.1%(95%CI,8.7%-43.5%),四肢为17.3%(95%CI,8.2%-26.5%),手和足无显著反应。
应鼓励进行长时间光疗以提高白癜风的治疗反应。预计面部和颈部反应最大。