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从分子层面重新定义小肠腺癌以加速精准医疗——一项多中心观察性队列生物标志物研究方案

Molecularly redefining small bowel adenocarcinoma to accelerate precision patient care - protocol of a multicenter observational cohort biomarker study.

作者信息

Døssing Rasmus Haunstrup, Broman Julia Johanna Almer, O'Rourke Colm J, Tabaksblat Elizaveta Mitkina, Andersen Jesper Bøje, Hansen Carsten Palnæs, Poulsen Tim Svenstrup, Høgdall Estrid V S, Schou Jakob Hagen Vasehus, Høgdall Dan

机构信息

Department of Oncology, Copenhagen University Hospital - Herlev and Gentofte, Borgmester Ib Juuls Vej 1, Herlev, 2730, Denmark.

Department of Health and Medical Sciences, Biotech Research and Innovation Center, University of Copenhagen, Ole Maaløes Vej 5, 4th Floor, Copenhagen N, 2200, Denmark.

出版信息

BMC Cancer. 2025 Jan 7;25(1):22. doi: 10.1186/s12885-024-13369-1.

Abstract

BACKGROUND

Small Bowel Adenocarcinoma (SBA) is a rare gastrointestinal cancer with a limited understanding of the molecular pathology. This study aims to bridge the knowledge gap, providing a robust molecular foundation for SBA and addressing the clinical challenges inherent in treating this orphan disease. The study proposes to redefine the clinical management for SBA patients through advanced molecular profiling techniques to improve potential precision medicine.

METHODS/DESIGN: This National multicenter, observational cohort study combines retrospective and prospective analyses across Danish University Hospitals. The study enrolls patients diagnosed with SBA, retrospectively from 2009 and prospectively from 2022 onwards. Molecular profiling, including DNA, RNA, and T-cell receptor sequencing, will be conducted on SBA tissue samples. The primary outcome is to categorize SBA into consensus molecular-guided subgroups. Secondary outcomes include correlating these subgroups with clinical features, treatment responses, and patient outcomes. Machine learning algorithms will be employed for bioinformatic analyses to interpret molecular data. Ethical approval has been obtained, and patient consent will be secured for the retrospective study component.

DISCUSSION

The molecular and clinical characterization of SBA is expected to add novel insights into the heterogeneity of this rare disease. By identifying molecular subgroups, the research could enable the development of personalized treatment strategies, a paradigm shift within SBA. The study acknowledges the challenges of working with orphan diseases, including limited patient numbers and diverse clinical presentations. However, its findings will have the potential to substantially impact future clinical practices and guide targeted therapies for SBA patients.

TRIAL REGISTRATION

ClinicalTrials.gov NCT06234306.

摘要

背景

小肠腺癌(SBA)是一种罕见的胃肠道癌症,对其分子病理学的了解有限。本研究旨在填补这一知识空白,为SBA提供坚实的分子基础,并应对治疗这种罕见疾病所固有的临床挑战。该研究提议通过先进的分子分析技术重新定义SBA患者的临床管理,以改善潜在的精准医学。

方法/设计:这项全国性多中心观察性队列研究结合了丹麦大学医院的回顾性和前瞻性分析。该研究招募被诊断为SBA的患者,回顾性分析从2009年开始,前瞻性分析从2022年起。将对SBA组织样本进行分子分析,包括DNA、RNA和T细胞受体测序。主要结果是将SBA分类为共识分子引导的亚组。次要结果包括将这些亚组与临床特征、治疗反应和患者预后相关联。机器学习算法将用于生物信息学分析以解释分子数据。已获得伦理批准,并将为回顾性研究部分获得患者同意。

讨论

SBA的分子和临床特征有望为这种罕见疾病的异质性提供新的见解。通过识别分子亚组,该研究可以推动个性化治疗策略的发展,这是SBA领域的一个范式转变。该研究认识到研究罕见疾病的挑战,包括患者数量有限和临床表现多样。然而,其研究结果有可能对未来的临床实践产生重大影响,并为SBA患者指导靶向治疗。

试验注册

ClinicalTrials.gov NCT06234306。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1014/11707884/d1bd85a394cd/12885_2024_13369_Fig1_HTML.jpg

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