2021
DOI: 10.1016/j.jaad.2020.04.160
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Chemoprevention of keratinocyte carcinoma and actinic keratosis in solid-organ transplant recipients: Systematic review and meta-analyses

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Cited by 14 publications
(14 citation statements)
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“…In the authors’ opinion, nicotinamide should be considered the first‐line agent because of its low cost, wide accessibility, minimal side effect profile, and inessential laboratory monitoring 1 . Although there is a lack of randomized, controlled trials comparing acitretin and nicotinamide chemoprevention, a systematic review and meta‐analysis determined that there was no significant difference between nicotinamide and acitretin in preventing keratinocyte carcinoma in SOTRs 4 . Based on our experience, we recommend that patients who had two or more NMSC in 1 year or a history of five NMSC take nicotinamide 500 mg BID.…”
Section: Discussionmentioning
confidence: 99%
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“…In the authors’ opinion, nicotinamide should be considered the first‐line agent because of its low cost, wide accessibility, minimal side effect profile, and inessential laboratory monitoring 1 . Although there is a lack of randomized, controlled trials comparing acitretin and nicotinamide chemoprevention, a systematic review and meta‐analysis determined that there was no significant difference between nicotinamide and acitretin in preventing keratinocyte carcinoma in SOTRs 4 . Based on our experience, we recommend that patients who had two or more NMSC in 1 year or a history of five NMSC take nicotinamide 500 mg BID.…”
Section: Discussionmentioning
confidence: 99%
“…1 Although there is a lack of randomized, controlled trials comparing acitretin and nicotinamide chemoprevention, a systematic review and meta-analysis determined that there was no significant difference between nicotinamide and acitretin in preventing keratinocyte carcinoma in SOTRs. 4 Based on our experience, we recommend that patients who had two or more NMSC in 1 year or a history of five NMSC take nicotinamide 500 mg BID. If there is no improvement in the rate of NMSC development after 6 months, the patient is switched to acitretin and dosed as previously described (see above).…”
Section: Discussionmentioning
confidence: 99%
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“…Another crucial confounding variable is concurrent systemic chemoprevention with acitretin, previously demonstrated to be effective in OTRs, 9 which was allowed during the SPOT trial and was more frequent in the 5‐FU group. Further trials should also consider using the core outcome set for AK trials, 10 which aims to homogenize outcome measures across studies to allow comparability and meta‐analyses – with such a core outcome set not being available when the SPOT trial was implemented.…”
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confidence: 99%