Bath-Hextall F, Leonardi-Bee J, Somchand N, Webster A, Delitt J, Perkins W
School of Nursing, University of Nottingham, Faculty of Medicine and Health Science, Room D83, Medical School, Queens Medical Centre, Nottingham, UK, NG7 2UH.
Cochrane Database Syst Rev. 2007 Oct 17;2007(4):CD005414. doi: 10.1002/14651858.CD005414.pub2.
Some groups of people have a greater risk of developing common non-melanoma skin cancers (NMSC).
To evaluate interventions for preventing NMSC in people at high risk of developing NMSC.
We searched the Cochrane Skin Group Specialised Register (March 2007), the Cochrane Central Register of Controlled Trials (The Cochrane Library Issue 1, 2007, MEDLINE (from 2003 to March 2007), EMBASE (from 2005 to March 2007), the metaRegister of Controlled Trials (February 2007). References from trials and reviews were also searched. Pharmaceutical companies were contacted for unpublished trials.
Randomised controlled trials of adults and children at high risk of developing NMSC.
Two review authors independently selected studies and assessed their methodological quality.
We identified 10 trials (7,229 participants) that assessed a variety of interventions. One trial found T4N5 liposome lotion significantly reduced the rate of appearance of new BCCs in people with xeroderma pigmentosum. One of three trials of renal transplant recipients showed a significantly reduced risk of new NMSCs when acitretin was compared to placebo (relative risk (RR) 0.22 95% confidence interval (CI) 0.06 to 0.90) and no significant difference in risk of adverse events in two trials (RR 1.80, 95% CI 0.70 to 4.61). In three trials conducted in people with a history of NMSC, the evidence was inconclusive for the development of BCCs for retinol or isoretinoin. However the risk of a new SCC in one trial (HR 1.79, 95% CI 1.16 to 2.76) and adverse events in another trial (RR 1.76 95% CI 1.57 to 1.97) were significantly increased in the isotretinoin group compared with placebo. In one trial selenium showed a reduced risk of other types of cancer compared with placebo (RR 0.65, 95% CI 0.50 to 0.85) but also a significantly elevated risk of a new NMSC (HR 1.17 95% CI 1.02 to 1.34). The evidence for one trial of beta-carotene was inconclusive; and there was a trend towards fewer new NMSC in a trial of a reduced fat diet (RR 0.16, 95% CI 0.02 to 1.31), p=0.09.
AUTHORS' CONCLUSIONS: Some preventative treatments may benefit people at high risk of developing NMSC, but the ability to draw firm conclusions is limited by small numbers of trials, often with one trial per intervention or with inconsistent results between studies.
某些人群患常见非黑色素瘤皮肤癌(NMSC)的风险更高。
评估针对患NMSC高风险人群预防NMSC的干预措施。
我们检索了Cochrane皮肤组专业注册库(2007年3月)、Cochrane对照试验中心注册库(《Cochrane图书馆》2007年第1期)、MEDLINE(2003年至2007年3月)、EMBASE(2005年至2007年3月)、对照试验元注册库(2007年2月)。还检索了试验和综述中的参考文献。联系了制药公司以获取未发表的试验。
针对患NMSC高风险的成人和儿童的随机对照试验。
两位综述作者独立选择研究并评估其方法学质量。
我们确定了10项试验(7229名参与者),这些试验评估了多种干预措施。一项试验发现,T4N5脂质体洗剂可显著降低着色性干皮病患者新发基底细胞癌(BCC)的发生率。在三项针对肾移植受者的试验中,与安慰剂相比,阿维A治疗时新发NMSC的风险显著降低(相对风险(RR)0.22,95%置信区间(CI)0.06至0.90),且在两项试验中不良事件风险无显著差异(RR 1.80,95%CI 0.70至4.61)。在三项针对有NMSC病史人群的试验中,关于视黄醇或异维A酸对BCC发生情况的证据尚无定论。然而,与安慰剂相比,异维A酸组在一项试验中新发鳞状细胞癌(SCC)的风险显著增加(风险比(HR)1.79,95%CI 1.16至2.76),在另一项试验中不良事件风险也显著增加(RR 1.76,95%CI 1.57至1.97)。在一项试验中,与安慰剂相比,硒显示出其他类型癌症的风险降低(RR 0.65,95%CI 0.50至0.85),但新发NMSC的风险也显著升高(HR 1.17,95%CI 1.02至1.34)。一项关于β-胡萝卜素试验的证据尚无定论;在一项低脂饮食试验中,有新发NMSC数量减少的趋势(RR 0.16,95%CI 0.02至1.31),p = 0.09。
一些预防性治疗可能使患NMSC高风险人群受益,但由于试验数量少(通常每种干预措施仅有一项试验,或研究结果不一致),得出确凿结论的能力有限。