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Nicotinamide for Skin-Cancer Chemoprevention in Transplant Recipients

医学 皮肤癌 基底细胞癌 烟酰胺 安慰剂 皮肤病科 内科学 胃肠病学 癌症 器官移植 角质形成细胞 相对风险 入射(几何) 随机化 移植 外科 随机对照试验 基底细胞 置信区间 病理 体外 化学 替代医学 物理 光学 生物化学
作者
Nicholas Allen,Andrew Martin,Victoria A. Snaidr,Renee Eggins,Alvin H Chong,Pablo Fernández‐Peñas,Douglas L. Gin,Shireen Sidhu,Vanessa L Paddon,Leith Banney,Adrian Lim,Edward Upjohn,Helmut Schaider,Aparna D Ganhewa,Jennifer Nguyen,Catriona McKenzie,Saurabh Prakash,Catriona McLean,Alistair Lochhead,Jan Ibbetson,Andrew Dettrick,Anthony Landgren,Katherine J Allnutt,Clare Allison,Rachael Davenport,Blake P Mumford,Brittany Wong,Brendan Stagg,Alexander Tedman,Hannah Gribbin,Harrison A. Edwards,Nicholas De Rosa,T. D. Stewart,Brent J Doolan,Yonatan Kok,Kate Simpson,Zhi M Low,Tom Kovitwanichkanont,Richard A. Scolyer,Haryana M. Dhillon,Janette L. Vardy,Steven J. Chadban,David G. Bowen,Andrew C. Chen,Diona L. Damian
出处
期刊:The New England Journal of Medicine [Massachusetts Medical Society]
卷期号:388 (9): 804-812 被引量:22
标识
DOI:10.1056/nejmoa2203086
摘要

Immunosuppressed organ-transplant recipients have an increased incidence of, and mortality from, skin cancer. Nicotinamide (vitamin B3) enhances the repair of ultraviolet (UV) radiation–induced DNA damage, reduces the cutaneous immunosuppressive effects of UV radiation, and reduces the incidence of keratinocyte cancers (including squamous-cell and basal-cell carcinomas) and actinic keratoses among high-risk immunocompetent patients. Whether oral nicotinamide is useful for skin-cancer chemoprevention in organ-transplant recipients is unclear. Download a PDF of the Research Summary. In this phase 3 trial, we randomly assigned, in a 1:1 ratio, organ-transplant recipients who had had at least two keratinocyte cancers in the past 5 years to receive 500 mg of nicotinamide or placebo twice daily for 12 months. Participants were examined for skin lesions by dermatologists at 3-month intervals for 12 months. The primary end point was the number of new keratinocyte cancers during the 12-month intervention period. Secondary end points included the numbers of squamous-cell and basal-cell carcinomas during the 12-month intervention period, the number of actinic keratoses until 6 months after randomization, safety, and quality of life. A total of 158 participants were enrolled, with 79 assigned to the nicotinamide group and 79 to the placebo group. The trial was stopped early owing to poor recruitment. At 12 months, there were 207 new keratinocyte cancers in the nicotinamide group and 210 in the placebo group (rate ratio, 1.0; 95% confidence interval, 0.8 to 1.3; P=0.96). No significant between-group differences in squamous-cell and basal-cell carcinoma counts, actinic keratosis counts, or quality-of-life scores were observed. Adverse events and changes in blood or urine laboratory variables were similar in the two groups. In this 12-month, placebo-controlled trial, oral nicotinamide therapy did not lead to lower numbers of keratinocyte cancers or actinic keratoses in immunosuppressed solid-organ transplant recipients. (Funded by the National Health and Medical Research Council; ONTRANS Australian New Zealand Clinical Trials Registry number, ACTRN12617000599370.) QUICK TAKE VIDEO SUMMARYNicotinamide for Skin-Cancer Prevention after Transplantation 01:57
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