Pellegrini Cristina, Caini Saverio, Gaeta Aurora, Lucantonio Eleonora, Mastrangelo Mirco, Bruni Manfredo, Esposito Maria, Doccioli Chiara, Queirolo Paola, Tosti Giulio, Raimondi Sara, Gandini Sara, Fargnoli Maria Concetta
Department of Biotechnological and Applied Clinical Sciences, University of L'Aquila, 67100 L'Aquila, Italy.
Cancer Risk Factors and Lifestyle Epidemiology Unit, Institute for Cancer Research, Prevention and Clinical Network (ISPRO), 50139 Florence, Italy.
Cancers (Basel). 2024 Nov 5;16(22):3734. doi: 10.3390/cancers16223734.
Several studies have described how the restrictive measures due to COVID-19 have delayed melanoma diagnoses, resulting in an increased rate of more severe cases. Summarizing the sparse results in this context might help to understand the real impact of the COVID-19 pandemic on melanoma. We conducted a systematic review and meta-analysis to investigate how the clinical and prognostic factors of new melanoma diagnoses changed after COVID-19.
A literature search in MEDLINE, EMBASE, and Scopus was conducted in September 2023. We included studies published in peer-reviewed journals reporting histopathological data on new diagnoses of cutaneous melanoma in adult patients during and/or after the lockdown compared to those diagnosed before the COVID-19 pandemic. A meta-analysis was conducted utilizing a random effects model. The between-study heterogeneity was assessed via Higgins's I statistic. Publication bias was assessed using the Begg and Egger test. This study adhered to the updated PRISMA guidelines. The primary outcome was a comparison of melanoma thickness between the pre-COVID-19 and post-lockdown periods. The secondary outcomes were evaluations of the histopathological subtype, stage, and presence of ulceration and mitosis in melanomas diagnosed in these two pandemic phases.
The study included 45 articles. We found a significantly higher proportion of all factors indicating worse prognosis in the post-lockdown period compared to the pre-COVID-19 phase, including high thickness (SOR = 1.14, 95%CI 1.08-1.20 for 1-2 mm; SOR = 1.62, 95%CI 1.08-2.40, for >2 mm), the presence of ulcerations (SOR = 1.35, 95%CI 1.18-1.54), nodular subtype (SOR = 1.19, 95%CI 1.07-1.32), the presence of mitosis (SOR = 1.57, 95% CI 1.17-2.11), and stage III (SOR = 1.39, 95%CI 1.19-1.52) and IV (SOR = 1.44, 95%CI 1.26-1.63). Limitations include the limited studies' geographical distribution and moderate heterogeneity affecting meta-analysis estimates.
Our meta-analysis provided evidence of more advanced melanomas diagnosed in the post-COVID-19 pandemic period, emphasizing the importance of creating and updating pandemic preparedness plans to limit the impact of any future events on oncological care.
多项研究描述了由于新冠疫情实施的限制措施如何延迟了黑色素瘤的诊断,导致更严重病例的比例增加。总结这方面稀少的研究结果可能有助于理解新冠疫情对黑色素瘤的实际影响。我们进行了一项系统综述和荟萃分析,以研究新冠疫情后新诊断黑色素瘤的临床和预后因素如何变化。
2023年9月在MEDLINE、EMBASE和Scopus数据库进行了文献检索。我们纳入了发表在同行评审期刊上的研究,这些研究报告了与新冠疫情大流行前诊断的成年患者相比,在封锁期间和/或之后新诊断皮肤黑色素瘤的组织病理学数据。使用随机效应模型进行荟萃分析。通过希金斯I统计量评估研究间的异质性。使用Begg和Egger检验评估发表偏倚。本研究遵循更新后的PRISMA指南。主要结果是比较新冠疫情前和封锁后时期黑色素瘤的厚度。次要结果是评估在这两个大流行阶段诊断的黑色素瘤的组织病理学亚型、分期以及溃疡和有丝分裂的存在情况。
该研究纳入了45篇文章。我们发现,与新冠疫情前阶段相比,封锁后时期所有表明预后较差的因素比例显著更高,包括厚度较大(1 - 2毫米时,优势比[SOR]=1.14,95%置信区间[CI]为1.08 - 1.20;>2毫米时,SOR = 1.62,95%CI为1.08 - 2.40)、存在溃疡(SOR = 1.35,95%CI为1.18 - 1.54)、结节亚型(SOR = 1.19,95%CI为1.07 - 1.32)、存在有丝分裂(SOR = 1.57,95%CI为1.17 - 2.11)以及III期(SOR = 1.39,95%CI为1.19 - 1.52)和IV期(SOR = 1.44,95%CI为1.26 - 1.63)。局限性包括研究的地理分布有限以及影响荟萃分析估计的中度异质性。
我们的荟萃分析提供了证据,表明在新冠疫情大流行后诊断出的黑色素瘤病情更严重,强调了制定和更新大流行防范计划以限制未来任何事件对肿瘤护理影响的重要性。