Defining the high-risk category of patients with cutaneous melanoma: a practical tool based on prognostic modeling.

IF 3.9 3区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Frontiers in Molecular Biosciences Pub Date : 2025-02-07 eCollection Date: 2025-01-01 DOI:10.3389/fmolb.2025.1543148
Oleksandr Dudin, Ozar Mintser, Vitalii Gurianov, Nazarii Kobyliak, Denys Kozakov, Sofiia Livshun, Oksana Sulaieva
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Abstract

Introduction: Although most cutaneous melanoma (CM) in its early stages is treatable, the risk of recurrence remains high and there is a particular ambiguity on patients prognosis. This drives to identification of prognostic biomarkers for predicting CM recurrence to guide appropriate treatment in patients with localized melanoma.

Aim: This study aimed to develop a prognostic model for assessing the risk of recurrence in patients with CM, enabling prompt prognosis-driven further clinical decision-making for high-risk patients.

Materials and methods: This case-control study included 172 patients with CM recurrence (high-risk group) and 30 patients with stable remission (low-risk group) 3 years after primary diagnosis. The impact of sex, age at diagnosis, anatomical site, histological characteristics (the histological type, pathological stage, ulceration; the depth of invasion, mitotic rate, lymphovascular invasion, neurotropism, association with a nevus, tumor-infiltrating lymphocyte density, tumor regression and BRAF codon 600 mutation status) on CM recurrence was evaluated.

Results: Five independent variables, including nodal status, a high mitotic rate, Breslow thickness, lymphovascular invasion, perineural invasion and regression features were identified as the most significant. A 5-factor logistic regression model was developed to assess the risk of melanoma recurrence. The sensitivity and specificity of the model were 86.1% and 72.7%, respectively.

Conclusion: The developed model, which relies on routine histological features, allows the identification of individuals at high risk of CM recurrence to tailor their further management.

定义皮肤黑色素瘤患者的高风险类别:基于预后模型的实用工具。
虽然大多数皮肤黑色素瘤(CM)在其早期阶段是可以治疗的,但复发的风险仍然很高,并且患者的预后特别不明确。这推动了预测CM复发的预后生物标志物的鉴定,以指导局部黑色素瘤患者的适当治疗。目的:本研究旨在建立一个评估CM患者复发风险的预后模型,使高风险患者能够及时做出预后驱动的进一步临床决策。材料与方法:本病例对照研究纳入172例CM复发患者(高危组)和30例CM缓解稳定的患者(低危组)。性别、诊断年龄、解剖部位、组织学特征(组织学类型、病理分期、溃疡;评估浸润深度、有丝分裂率、淋巴血管浸润、嗜神经性、与痣的相关性、肿瘤浸润淋巴细胞密度、肿瘤消退和BRAF密码子600突变状态)对CM复发的影响。结果:淋巴结状态、高有丝分裂率、Breslow厚度、淋巴血管侵犯、神经周围侵犯和消退特征等5个自变量被认为是最重要的。采用五因素logistic回归模型评估黑素瘤复发风险。该模型的敏感性为86.1%,特异性为72.7%。结论:开发的模型依赖于常规组织学特征,允许识别CM复发高风险个体,以定制其进一步的管理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Frontiers in Molecular Biosciences
Frontiers in Molecular Biosciences Biochemistry, Genetics and Molecular Biology-Biochemistry
CiteScore
7.20
自引率
4.00%
发文量
1361
审稿时长
14 weeks
期刊介绍: Much of contemporary investigation in the life sciences is devoted to the molecular-scale understanding of the relationships between genes and the environment — in particular, dynamic alterations in the levels, modifications, and interactions of cellular effectors, including proteins. Frontiers in Molecular Biosciences offers an international publication platform for basic as well as applied research; we encourage contributions spanning both established and emerging areas of biology. To this end, the journal draws from empirical disciplines such as structural biology, enzymology, biochemistry, and biophysics, capitalizing as well on the technological advancements that have enabled metabolomics and proteomics measurements in massively parallel throughput, and the development of robust and innovative computational biology strategies. We also recognize influences from medicine and technology, welcoming studies in molecular genetics, molecular diagnostics and therapeutics, and nanotechnology. Our ultimate objective is the comprehensive illustration of the molecular mechanisms regulating proteins, nucleic acids, carbohydrates, lipids, and small metabolites in organisms across all branches of life. In addition to interesting new findings, techniques, and applications, Frontiers in Molecular Biosciences will consider new testable hypotheses to inspire different perspectives and stimulate scientific dialogue. The integration of in silico, in vitro, and in vivo approaches will benefit endeavors across all domains of the life sciences.
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