Joly-Chevrier Maxine, Gélinas Alexa, Ghazal Stephanie, Moussa Sarah, McCuaig Catherine C, Piram Maryam, Mereniuk Alexandra, Litvinov Ivan V, Osman Mohammed, Pehr Kevin, Netchiporouk Elena
Faculty of Medicine, Université de Montréal, Montreal, QC H3T 1J4, Canada.
Division of Dermatology, McGill University Health Centre, Montreal, QC H4A 3J1, Canada.
Cancers (Basel). 2023 Sep 7;15(18):4450. doi: 10.3390/cancers15184450.
Morphea is an autoimmune fibrotic skin disease. Eosinophilic fasciitis (EF) is considered to belong to the severe spectrum of morphea. We conducted a scoping review assessing the risk of secondary cancer among morphea/EF patients, paraneoplastic morphea/EF and morphea/EF developing secondary to cancer therapy. The search was conducted using MEDLINE, Embase, Cochrane databases for articles published from inception to September 2022 following the Preferred Reporting Items for Systematic reviews and Meta-Analyses for Scoping Reviews (PRISMA-ScR) guidelines with no language or date restrictions. Two hundred and one studies were included. Of these, 32 studies reported on secondary cancer in morphea/EF patients, 45 on paraneoplastic morphea/EF and 125 on cancer-treatment-induced morphea/EF. While the current evidence remains limited, data suggest an increased risk of secondary cutaneous and possibly pancreatic malignancy in morphea patients, particularly the generalized subtype. There were insufficient data for EF. On the other hand, paraneoplastic morphea was anecdotal, whereas several observational studies suggested that ~10% of EF cases may be paraneoplastic, primarily in the context of hematologic malignancies. Radiotherapy-induced morphea is rare, seen in ~0.2% of treated patients and is usually localized to the treatment site, except in patients with pre-existing autoimmunity. While chemotherapy-induced cases are reported, immunotherapy morphea/EF cases are emerging and are preferentially seen with PD-1 and not CTLA-4 inhibitors. This study is limited by the type of articles included (case reports, case series and observational studies), and hence, additional research on this important topic is needed.
硬斑病是一种自身免疫性纤维化皮肤病。嗜酸性筋膜炎(EF)被认为属于硬斑病的严重类型。我们进行了一项范围综述,评估硬斑病/EF患者、副肿瘤性硬斑病/EF以及癌症治疗后继发性硬斑病/EF的继发癌症风险。检索使用MEDLINE、Embase、Cochrane数据库,以查找自数据库创建至2022年9月发表的文章,遵循系统评价和范围综述的首选报告项目(PRISMA-ScR)指南,无语言或日期限制。纳入了201项研究。其中,32项研究报告了硬斑病/EF患者的继发癌症,45项报告了副肿瘤性硬斑病/EF,125项报告了癌症治疗引起的硬斑病/EF。虽然目前的证据仍然有限,但数据表明硬斑病患者继发皮肤癌以及可能的胰腺癌的风险增加,尤其是泛发型。关于EF的数据不足。另一方面,副肿瘤性硬斑病的报道较少,而几项观察性研究表明,约10%的EF病例可能是副肿瘤性的,主要发生在血液系统恶性肿瘤的背景下。放疗引起的硬斑病很少见,在约0.2%的接受治疗患者中出现,通常局限于治疗部位,但已有自身免疫性疾病的患者除外。虽然有化疗引起硬斑病的报道,但免疫治疗相关的硬斑病/EF病例正在出现,且优先见于使用PD-1而非CTLA-4抑制剂的患者。本研究受所纳入文章类型(病例报告、病例系列和观察性研究)的限制,因此,需要对这一重要主题进行更多研究。