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[膀胱肌层浸润性和转移性尿路上皮癌:组织病理学、分子和免疫预后及预测因素的现状]

[Muscle-invasive and metastatic urothelial carcinoma of the urinary bladder : Current state of histopathologic, molecular, and immunologic prognostic and predictive factors].

作者信息

Bertz Simone, Bahlinger Veronika, Lange Fabienne, Hartmann Arndt, Eckstein Markus

机构信息

Institut für Pathologie, Universitätsklinikum Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), Krankenhausstraße 8-10, 91054, Erlangen, Deutschland.

Comprehensive Cancer Center EMN, Universitätsklinikum Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), Erlangen, Deutschland.

出版信息

Pathologie (Heidelb). 2024 Nov;45(6):363-370. doi: 10.1007/s00292-024-01347-0. Epub 2024 Aug 7.

Abstract

BACKGROUND

Muscle-invasive and metastatic urothelial carcinoma (UC) represents a heterogeneous disease entity with numerous morphological, molecular, and immunological phenotypes.

AIMS

This article aims to provide an overview of current histopathological, molecular, and immunological prognostic and predictive factors in muscle-invasive and metastatic UC.

RESULTS AND DISCUSSION

Muscle-invasive and metastatic UC exhibits a wide range of divergent differentiations and histological subtypes. The correct diagnosis of these morphological variants is essential, as they may determine the clinical course and may also present specific and potentially therapeutically targetable molecular alterations (e.g., HER2 alterations in micropapillary UC). The morphological subtypes largely correlate with the six molecular consensus subtypes. Furthermore, morphological and molecular subtypes are associated with immunological properties that are relevant for modern immunotherapies, such as the PD-L1 status. Numerous immunotherapy studies in the setting of curatively treatable muscle-invasive UC will be reported in 2024 and 2025, likely leading to an increasing number of PD-L1 testing indications.

摘要

背景

肌层浸润性和转移性尿路上皮癌(UC)是一种具有多种形态、分子和免疫表型的异质性疾病实体。

目的

本文旨在概述肌层浸润性和转移性UC当前的组织病理学、分子和免疫预后及预测因素。

结果与讨论

肌层浸润性和转移性UC表现出广泛的不同分化程度和组织学亚型。正确诊断这些形态学变异至关重要,因为它们可能决定临床病程,还可能呈现特定的、潜在可靶向治疗的分子改变(例如,微乳头型UC中的HER2改变)。形态学亚型在很大程度上与六种分子共识亚型相关。此外,形态学和分子亚型与现代免疫疗法相关的免疫特性有关,如PD-L1状态。2024年和2025年将报告许多针对可治愈性肌层浸润性UC的免疫治疗研究,这可能会导致PD-L1检测适应证的数量增加。

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