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1.
N Engl J Med ; 388(9): 804-812, 2023 Mar 02.
Article En | MEDLINE | ID: mdl-36856616

BACKGROUND: 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. METHODS: 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. RESULTS: 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. CONCLUSIONS: 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.).


Antineoplastic Agents , Niacinamide , Skin Neoplasms , Transplant Recipients , Humans , Australia , Carcinoma, Basal Cell/etiology , Carcinoma, Basal Cell/prevention & control , Carcinoma, Squamous Cell/etiology , Carcinoma, Squamous Cell/prevention & control , Chemoprevention , Keratosis, Actinic/etiology , Keratosis, Actinic/prevention & control , Niacinamide/administration & dosage , Niacinamide/therapeutic use , Quality of Life , Skin Neoplasms/etiology , Skin Neoplasms/prevention & control , Immunocompromised Host , Organ Transplantation/adverse effects , Antineoplastic Agents/administration & dosage , Antineoplastic Agents/therapeutic use , Ultraviolet Rays/adverse effects
2.
Exp Dermatol ; 28 Suppl 1: 15-22, 2019 02.
Article En | MEDLINE | ID: mdl-30698874

Nicotinamide is a water-soluble vitamin B3 derivative that has many roles in medicine. This review examines the role of nicotinamide in dermatology and its actions in preventing photoageing and skin cancers in humans. Nicotinamide prevents ultraviolet radiation (UV) from reducing ATP levels and inhibiting glycolysis, thus preventing the UV radiation-induced energy crisis. This enhances DNA repair and reduces UV-induced suppression of immunity. Randomised controlled clinical trials have also shown that nicotinamide reduces transepidermal water loss and the development of new non-melanoma skin cancers in high-risk humans. This review also examines nicotinamide's safety profile.


Niacinamide/adverse effects , Niacinamide/therapeutic use , Skin Aging/drug effects , Skin Neoplasms/prevention & control , Adenosine Triphosphate/metabolism , Animals , Anti-Inflammatory Agents , Chemoprevention , DNA Damage , DNA Repair , Dermatology/methods , Female , Gastrointestinal Tract/drug effects , Glycolysis , Humans , Inflammation , Keratosis, Actinic/metabolism , Kidney Failure, Chronic/complications , Liver/drug effects , Milk, Human/drug effects , Patient Safety , Pregnancy , Randomized Controlled Trials as Topic , Skin Aging/radiation effects , Ultraviolet Rays , Vitamin B Complex/pharmacology
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