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病理学家在癌症生物标志物驱动的临床试验设计与实施中的作用:欧洲病理学会立场文件

The role of the pathologist in the design and conducting of biomarker-driven clinical trials in cancer: position paper of the European Society of Pathology.

作者信息

Matias-Guiu Xavier, Raspollini Maria Rosaria, Kulka Janina, Ryska Ales, Al Dieri Raed, Schirmacher Peter

机构信息

Hospital Universitari Arnau de Vilanova, Universitat de Lleida, IRBLleida, CIBERONC, Lleida, Spain.

Hospital U de Bellvitge, IDIBELL, University of Barcelona, Barcelona, Spain.

出版信息

Virchows Arch. 2025 Feb;486(2):207-214. doi: 10.1007/s00428-024-04005-1. Epub 2024 Dec 17.

Abstract

Clinical trials in oncology are important tools to identify and establish new effective drugs for cancer treatment. Since the development of the concept of precision oncology, a huge number of multi-centric biomarker-driven clinical trials have been performed and promoted by either academic institutions or pharmaceutical companies. In this scenario, the role of pathologists is essential in multiple aspects, with new challenges that should be addressed. In this position paper of the European Society of Pathology, the role of pathologists as contributors to the design of the clinical trial, as local collaborators, or as members of central review laboratories is discussed. Moreover, the paper emphasizes the important role of pathologists in guiding methods and criteria of tissue biomarker testing in the biomarker-driven clinical trials. The paper also addresses issues regarding quality control, training, and the possible role of digital pathology.

摘要

肿瘤学临床试验是识别和确立用于癌症治疗的新型有效药物的重要工具。自从精准肿瘤学概念出现以来,学术机构或制药公司开展并推动了大量以生物标志物为驱动的多中心临床试验。在这种情况下,病理学家在多个方面发挥着至关重要的作用,同时也面临着需要应对的新挑战。在欧洲病理学会的这份立场文件中,讨论了病理学家作为临床试验设计贡献者、当地合作者或中央审查实验室成员的角色。此外,本文强调了病理学家在指导生物标志物驱动的临床试验中组织生物标志物检测方法和标准方面的重要作用。本文还讨论了质量控制、培训以及数字病理学可能发挥的作用等问题。

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