Hwang Jonathan C, Savage Kevin T, Pugliano-Mauro Melissa
University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.
Department of Dermatology, University of Pittsburgh Medical Center, 3708 Fifth Avenue, Suite 500.68, Pittsburgh, PA, 15213, USA.
Arch Dermatol Res. 2025 Jun 11;317(1):807. doi: 10.1007/s00403-025-04296-7.
Nicotinamide has many well-established chemopreventive properties in protecting against ultraviolet-induced skin damage, mitigating inflammation, and reducing keratinocyte carcinoma (KC) development among immunocompetent individuals. Its effectiveness in immunosuppressed patients, however, is unclear. There is conflicting research on whether nicotinamide effectively decreases KCs in immunosuppressed solid organ transplant recipients (SOTRs). This study assesses the effectiveness of nicotinamide in the secondary prevention of KC in immunosuppressed patients. We conducted a retrospective cohort study in a single tertiary care institution. The primary outcome was KC incidence in the year before and after nicotinamide supplementation. Secondary outcomes included the incidence of invasive squamous cell carcinoma (SCC), SCC in situ (SCCis), and basal cell carcinoma (BCC) over one- and two-year intervals. All included patients had taken oral nicotinamide, 500 milligrams twice daily, for at least one year. A total of 47 SOTRs (74.5% male; mean age 65.2 years) were included in our retrospective cohort study. Of 81 patients initially screened, 34 were excluded due to inadequate follow-up, dermatologic care outside our institution, or early discontinuation of nicotinamide. At one year post-nicotinamide supplementation, total KC incidence decreased from 224 (78 SCC, 103 SCCis, 43 BCC) to 121 cases (40 SCC, 55 SCCis, 26 BCC), a mean reduction of 2.19 KCs (95% CI: -3.48 to -0.90; p = 0.0012). Significant reductions were observed in SCC (mean decrease of 1.15; 95% CI: -1.78 to -0.52; p = 0.00081) and SCCis (mean decrease of 1.37; 95% CI: -2.61 to -0.13; p = 0.032). BCC reduction was not statistically significant (p = 0.13). In the 31 patients with two-year follow-up data, KC incidence declined from 234 to 167, a mean reduction of 2.18 KCs (95% CI: -4.18 to -0.14; p = 0.037). Sensitivity analyses excluding patients on concomitant acitretin confirmed that reductions in total KC incidence maintained significance at both one-year and two-year intervals. Nicotinamide supplementation significantly decreased KC incidence in immunosuppressed SOTRs over the one-year and two-year intervals. We recommend nicotinamide as a low-risk, low-cost chemopreventive supplement for reducing KCs in SOTRs.
烟酰胺在预防紫外线引起的皮肤损伤、减轻炎症以及减少免疫功能正常个体的角质形成细胞癌(KC)发生方面具有许多已得到充分证实的化学预防特性。然而,其在免疫抑制患者中的有效性尚不清楚。关于烟酰胺是否能有效减少免疫抑制实体器官移植受者(SOTR)中的KC,存在相互矛盾的研究。本研究评估了烟酰胺在免疫抑制患者KC二级预防中的有效性。我们在一家三级医疗中心进行了一项回顾性队列研究。主要结局是补充烟酰胺前后一年的KC发病率。次要结局包括一年和两年期间侵袭性鳞状细胞癌(SCC)、原位鳞状细胞癌(SCCis)和基底细胞癌(BCC)的发病率。所有纳入患者均口服烟酰胺,每日两次,每次500毫克,至少服用一年。我们的回顾性队列研究共纳入了47例SOTR(男性占74.5%;平均年龄65.2岁)。在最初筛查的81例患者中,34例因随访不足、在本机构以外接受皮肤科护理或过早停用烟酰胺而被排除。补充烟酰胺一年后,KC总发病率从224例(78例SCC、103例SCCis、43例BCC)降至121例(40例SCC、55例SCCis、26例BCC),平均减少2.19例KC(95%CI:-3.48至-0.90;p = 0.0012)。SCC(平均减少1.15;95%CI:-1.78至-0.52;p = 0.00081)和SCCis(平均减少1.37;95%CI:-2.61至-0.13;p = 0.032)均有显著下降。BCC的减少无统计学意义(p = 0.13)。在有两年随访数据的31例患者中,KC发病率从234例降至167例,平均减少2.18例KC(95%CI:-4.18至-0.14;p = 0.037)。排除同时服用阿维A的患者进行的敏感性分析证实,在一年和两年期间,KC总发病率的降低均保持显著。在一年和两年期间,补充烟酰胺显著降低了免疫抑制SOTR中的KC发病率。我们推荐烟酰胺作为一种低风险、低成本的化学预防补充剂,用于减少SOTR中的KC。