Primary Bone Vascular Neoplasms: An Integrated Biological Perspective from Bone Pathology to Precision Oncology.

IF 4.8 2区 医学 Q1 ONCOLOGY
Cancers Pub Date : 2026-10-07 DOI:10.3390/cancers18193229
Aikaterini Anetaki, Constantine Anetakis, Ioannis Chaniotakis, Christos Mpogiatzis, Anna Goussia, Dionysios J Papachristou, Mattheos Bobos
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引用次数: 0

Abstract

Primary bone vascular neoplasms comprise a rare and biologically heterogeneous group of endothelial tumors encompassing benign, intermediate, and malignant entities with distinct clinicopathological, molecular, and prognostic characteristics. These tumors remain diagnostically and biologically challenging because of overlapping histopathological features, heterogeneous clinical behavior, evolving molecular landscapes, and limited disease-specific evidence. Advances in bone pathology, immunophenotyping, molecular diagnostics, and genomic profiling have substantially improved tumor classification and biological characterization. Importantly, contemporary classification and molecular studies have also highlighted the biological heterogeneity of vascular lesions involving bone, distinguishing well-defined vascular neoplasms from vascular malformations and identifying additional molecularly defined entities relevant to osseous disease and differential diagnosis. Concurrently, increasing recognition of the bone microenvironment and osteoimmunology provides a broader framework for understanding interactions among endothelial, skeletal, stromal, and immune populations and the extracellular matrix, with potential relevance to angiogenesis, bone remodeling, and tumor biology. Previous authoritative syntheses have established the classification, molecular features, diagnosis, and clinical management of these neoplasms. However, comparatively limited attention has been devoted to integrating tumor-intrinsic alterations with vascular-bone crosstalk, extracellular-matrix and mechanobiological signaling, osteoimmune regulation, and emerging precision-oncology strategies. Building on these foundations, this review integrates current evidence on classification, molecular pathogenesis, the skeletal microenvironment, osteoimmunology, biomarkers, and precision oncology. Where relevant, molecularly defined vascular neoplasms and vascular anomalies involving bone are discussed to clarify classification, molecular context, and differential diagnosis without conflating these lesions with the principal WHO-defined primary vascular neoplasms of bone. Findings directly demonstrated in primary bone vascular neoplasms are distinguished from mechanistic concepts extrapolated from physiological bone biology, other bone tumors, or non-osseous vascular neoplasms. Through this evidence-calibrated approach, we propose an integrated vascular-bone-immune framework, identify key knowledge gaps, and define priorities for disease-specific translational research and more individualized patient management.

原发性骨血管肿瘤:从骨病理学到精确肿瘤学的综合生物学观点。
原发性骨血管肿瘤是一种罕见且生物异质性的内皮肿瘤,包括良性、中度和恶性肿瘤,具有不同的临床病理、分子和预后特征。由于重叠的组织病理学特征、异质的临床行为、不断发展的分子景观和有限的疾病特异性证据,这些肿瘤在诊断和生物学上仍然具有挑战性。骨病理学、免疫表型、分子诊断和基因组谱的进步大大改善了肿瘤的分类和生物学表征。重要的是,当代的分类和分子研究也强调了涉及骨骼的血管病变的生物学异质性,区分了明确的血管肿瘤和血管畸形,并确定了与骨性疾病和鉴别诊断相关的其他分子明确的实体。同时,对骨微环境和骨免疫学的日益认识为理解内皮、骨骼、基质、免疫群体和细胞外基质之间的相互作用提供了一个更广泛的框架,与血管生成、骨重塑和肿瘤生物学具有潜在的相关性。以前的权威综合已经建立了这些肿瘤的分类、分子特征、诊断和临床处理。然而,将肿瘤固有改变与血管-骨串扰、细胞外基质和机械生物学信号、骨免疫调节和新兴的精确肿瘤学策略结合起来的研究相对有限。在此基础上,本综述整合了分类、分子发病机制、骨骼微环境、骨免疫学、生物标志物和精确肿瘤学方面的最新证据。在相关的情况下,讨论分子定义的血管肿瘤和涉及骨骼的血管异常,以澄清分类、分子背景和鉴别诊断,而不将这些病变与世卫组织定义的主要原发性骨血管肿瘤混为一谈。原发性骨血管肿瘤的发现与从生理骨生物学、其他骨肿瘤或非骨血管肿瘤中推断出的机械概念不同。通过这种循证校准的方法,我们提出了一个整合的血管-骨-免疫框架,确定了关键的知识空白,并确定了疾病特异性转化研究和更个性化的患者管理的优先事项。
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
Cancers
Cancers Medicine-Oncology
CiteScore
8.00
自引率
9.60%
发文量
5371
审稿时长
18.07 days
期刊介绍: Cancers (ISSN 2072-6694) is an international, peer-reviewed open access journal on oncology. It publishes reviews, regular research papers and short communications. Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. There is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced.
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