Suppr超能文献

实时通过微阵列对肾移植适应证活检进行中央评估:INTERCOMEX 研究。

Real Time Central Assessment of Kidney Transplant Indication Biopsies by Microarrays: The INTERCOMEX Study.

机构信息

Alberta Transplant Applied Genomics Centre, Edmonton, AB, Canada.

Division of Nephrology and Transplant Immunology, Department of Medicine, University of Alberta, Edmonton, AB, Canada.

出版信息

Am J Transplant. 2017 Nov;17(11):2851-2862. doi: 10.1111/ajt.14329. Epub 2017 May 30.

Abstract

The authors conducted a prospective trial to assess the feasibility of real time central molecular assessment of kidney transplant biopsy samples from 10 North American or European centers. Biopsy samples taken 1 day to 34 years posttransplantation were stabilized in RNAlater, sent via courier overnight at ambient temperature to the central laboratory, and processed (29 h workflow) using microarrays to assess T cell- and antibody-mediated rejection (TCMR and ABMR, respectively). Of 538 biopsy samples submitted, 519 (96%) were sufficient for microarray analysis (average length, 3 mm). Automated reports were generated without knowledge of histology and HLA antibody, with diagnoses assigned based on Molecular Microscope Diagnostic System (MMDx) classifier algorithms and signed out by one observer. Agreement between MMDx and histology (balanced accuracy) was 77% for TCMR, 77% for ABMR, and 76% for no rejection. A classification tree derived to provide automated sign-outs predicted the observer sign-outs with >90% accuracy. In 451 biopsy samples where feedback was obtained, clinicians indicated that MMDx more frequently agreed with clinical judgment (87%) than did histology (80%) (p = 0.0042). In 81% of feedback forms, clinicians reported that MMDx increased confidence in management compared with conventional assessment alone. The authors conclude that real time central molecular assessment is feasible and offers a useful new dimension in biopsy interpretation. ClinicalTrials.gov NCT#01299168.

摘要

作者进行了一项前瞻性试验,以评估从 10 个北美或欧洲中心的肾移植活检样本中实时进行中央分子评估的可行性。在移植后 1 天至 34 年内采集的活检样本用 RNAlater 稳定,通过隔夜快递在环境温度下送至中央实验室,并使用微阵列进行处理(29 小时工作流程),以评估 T 细胞和抗体介导的排斥反应(TCMR 和 ABMR)。在提交的 538 个活检样本中,有 519 个(96%)足够进行微阵列分析(平均长度为 3 毫米)。自动报告是在不了解组织学和 HLA 抗体的情况下生成的,诊断是根据分子显微镜诊断系统(MMDx)分类器算法确定的,并由一名观察者签署。MMDx 与组织学之间的一致性(平衡准确性)分别为 TCMR 为 77%,ABMR 为 77%,无排斥反应为 76%。为提供自动签署而导出的分类树预测了观察者签署的准确率>90%。在获得反馈的 451 个活检样本中,临床医生表示,与组织学相比,MMDx 更频繁地与临床判断一致(87%对 80%)(p=0.0042)。在 81%的反馈表中,临床医生报告称,与单独进行常规评估相比,MMDx 增加了对管理的信心。作者得出结论,实时中央分子评估是可行的,并为活检解释提供了一个有用的新维度。ClinicalTrials.gov NCT#01299168。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验