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皮肤黑色素瘤临床病理特征的基于表型的无监督聚类

Unsupervised Phenotype-Based Clustering of Clinicopathologic Features in Cutaneous Melanoma.

作者信息

Rashid Sarem, Klebanov Nikolai, Lin William M, Tsao Hensin

机构信息

Wellman Center for Photomedicine, Massachusetts General Hospital, Boston, Massachusetts, USA.

Department of Dermatology, Massachusetts General Hospital, Boston, Massachusetts, USA.

出版信息

JID Innov. 2021 Aug 20;1(4):100047. doi: 10.1016/j.xjidi.2021.100047. eCollection 2021 Dec.

DOI:10.1016/j.xjidi.2021.100047
PMID:34909744
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8659382/
Abstract

Pathogenic phenotypes in cutaneous melanoma have been vastly cataloged, although these classifications lack concordance and are confined to either morphological or molecular contexts. In this study, we perform unsupervised k-medoids clustering as a machine learning technique of 2,978 primary cutaneous melanomas at Mass General Brigham and apply this information to elucidate computer-defined subsets within the clinicopathologic domain. We identified five optimally separated clusters of melanoma that occupied two distinct clinicopathologic subspaces: a lower-grade partition associated with common or dysplastic nevi (i.e., nevus-associated melanomas) and a higher-grade partition lacking precursor lesions (i.e., de novo melanomas). Our model found de novo melanomas to be more mitogenic, more ulcerative, and thicker than nevus-associated melanomas, in addition to harboring previously unreported differences in radial and vertical growth phase status. The utilization of mixed clinicopathologic variables, reflective of actual clinical data contained in surgical pathology reports, has the potential to increase the biological relevance of existing melanoma classification schemes and facilitate the discovery of new genomic subtypes.

摘要

皮肤黑色素瘤的致病表型已被大量分类,尽管这些分类缺乏一致性,且局限于形态学或分子背景。在本研究中,我们将无监督k-中心点聚类作为一种机器学习技术,应用于麻省总医院布莱根分院的2978例原发性皮肤黑色素瘤,并运用这些信息来阐明临床病理领域中计算机定义的子集。我们识别出了五个最佳分离的黑色素瘤簇,它们占据了两个不同的临床病理子空间:一个与普通或发育异常痣相关的低级别分区(即痣相关黑色素瘤)和一个缺乏前驱病变的高级别分区(即新发黑色素瘤)。我们的模型发现,新发黑色素瘤比痣相关黑色素瘤更具促有丝分裂活性、更易溃疡且更厚,此外还存在先前未报道的在放射状和垂直生长期状态方面的差异。利用反映手术病理报告中实际临床数据的混合临床病理变量,有可能提高现有黑色素瘤分类方案的生物学相关性,并促进新基因组亚型的发现。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6133/8659382/b81b4159f852/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6133/8659382/76e0a24ae67e/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6133/8659382/b8c6a646b0b1/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6133/8659382/b81b4159f852/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6133/8659382/76e0a24ae67e/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6133/8659382/b8c6a646b0b1/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6133/8659382/b81b4159f852/gr3.jpg

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J Eur Acad Dermatol Venereol. 2021 May;35(5):1111-1118. doi: 10.1111/jdv.17133. Epub 2021 Feb 23.
2
A multicentre study of naevus-associated melanoma vs. de novo melanoma, tumour thickness and body site differences.一项关于痣相关黑色素瘤与新发黑色素瘤、肿瘤厚度和身体部位差异的多中心研究。
Br J Dermatol. 2021 Jul;185(1):101-109. doi: 10.1111/bjd.19819. Epub 2021 Apr 1.
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Pre-clinical modeling of cutaneous melanoma.
皮肤黑色素瘤的临床前建模。
Nat Commun. 2020 Jun 5;11(1):2858. doi: 10.1038/s41467-020-15546-9.
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Melanoma pathology reporting and staging.黑素瘤病理学报告和分期。
Mod Pathol. 2020 Jan;33(Suppl 1):15-24. doi: 10.1038/s41379-019-0402-x. Epub 2019 Nov 22.
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Transcriptomic Analysis Reveals Prognostic Molecular Signatures of Stage I Melanoma.转录组分析揭示 I 期黑色素瘤的预后分子特征。
Clin Cancer Res. 2019 Dec 15;25(24):7424-7435. doi: 10.1158/1078-0432.CCR-18-3659. Epub 2019 Sep 12.
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Dysplastic vs. Common Naevus-associated vs. De novo Melanomas: An Observational Retrospective Study of 1,021 Patients.发育不良性黑色素瘤与普通痣相关黑色素瘤与新发黑色素瘤:1021 例患者的观察性回顾性研究。
Acta Derm Venereol. 2018 Jun 8;98(6):556-562. doi: 10.2340/00015555-2908.
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