Bile Floriana, Sparaco Maddalena, Ruocco Eleonora, Miele Giuseppina, Maida Elisabetta, Vele Renato, Mele Davide, Bonavita Simona, Lavorgna Luigi
Department of Advanced Medical and Surgical Sciences, 2nd Division of Neurology, University of Campania Luigi Vanvitelli, Via Sergio Pansini, 5, 80131 Naples, Italy.
2nd Division of Neurology, University Hospital of Campania Luigi Vanvitelli, 80131 Naples, Italy.
J Clin Med. 2024 Aug 29;13(17):5133. doi: 10.3390/jcm13175133.
Over the past 20 years, the treatment scenario of multiple sclerosis (MS) has radically changed, and an ever-increasing number of disease-modifying treatments has emerged. Among high-efficacy treatment agents, monoclonal antibodies (mAbs) have become a mainstay in a MS patient's treatment due to their targeted mechanism, high efficacy, and favorable risk profile. The latter varies from drug to drug and a skin cancer warning has emerged with sphingosine 1-phosphate receptor inhibitors. Several cases of skin malignancy in people with MS (pwMS) undergoing therapy with mAbs have also been described, but dermatological follow-up is not currently indicated. The aim of this review is to investigate cases of cutaneous malignancy during mAb therapy and to explore possible pathophysiological mechanisms to evaluate the potential need for regular dermatological follow-ups in pwMS treated with mAbs. A literature search for original articles and reviews in PubMed was conducted with no date restrictions. A total of 1019 results were retrieved. Duplicates were removed using Endnote and manually. Only peer-reviewed studies published in English were considered for inclusion. At the end of these screening procedures, 54 studies published between 2001 and 2024 that met the objectives of this review were selected and reported. The available data do not show a clear link between monoclonal antibody (mAb) treatment in pwMS and the risk of skin cancer. At present, these treatments remain contraindicated for people with cancer. Dermatological screening is advisable before starting mAb treatment in pwMS, and subsequent follow-ups should be individualized according to each patient's risk profile.
在过去20年中,多发性硬化症(MS)的治疗情况发生了根本性变化,出现了越来越多的疾病修正治疗方法。在高效治疗药物中,单克隆抗体(mAbs)由于其靶向作用机制、高效性和良好的风险特征,已成为MS患者治疗的主要手段。后者因药物而异,并且使用鞘氨醇1-磷酸受体抑制剂时出现了皮肤癌警告。也有几例接受mAbs治疗的MS患者(pwMS)发生皮肤恶性肿瘤的病例报道,但目前尚无皮肤科随访的指征。本综述的目的是调查mAb治疗期间皮肤恶性肿瘤的病例,并探讨可能的病理生理机制,以评估接受mAb治疗的pwMS定期进行皮肤科随访的潜在必要性。在PubMed上对原始文章和综述进行了无日期限制的文献检索。共检索到1019条结果。使用Endnote并手动去除重复项。仅纳入以英文发表的同行评审研究。在这些筛选程序结束时,选择并报告了2001年至2024年期间发表的54项符合本综述目标的研究。现有数据未显示pwMS中使用单克隆抗体(mAb)治疗与皮肤癌风险之间存在明确联系。目前,这些治疗方法对癌症患者仍然禁忌。在pwMS开始mAb治疗前建议进行皮肤科筛查,随后的随访应根据每位患者的风险特征进行个体化。