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分子检测结果报告:BRAF 突变报告的回顾性研究。

Reporting Results of Molecular Tests: A Retrospective Examination of BRAF Mutation Reporting.

作者信息

Treece Amanda L, Gulley Margaret L, Vasalos Patricia, Paquette Cherie, Lindeman Neal I, Jennings Lawrence J, Bartley Angela N

机构信息

From the Department of Pathology, University of Colorado Anschutz Medical Campus, Aurora (Dr Treece); the Department of Pathology and Laboratory Medicine, University of North Carolina, Chapel Hill (Dr Gulley); College of American Pathologists, Northfield, Illinois (Ms Vasalos); the Department of Pathology, Warren Alpert Medical School of Brown University, Providence, Rhode Island (Dr Paquette); the Department of Pathology, Brigham and Women's Hospital, Boston, Massachusetts (Dr Lindeman); the Department of Pathology, Ann and Robert H. Lurie Children's Hospital of Chicago, Northwestern University Feinberg School of Medicine, Chicago, Illinois (Dr Jennings); and the Department of Pathology and Laboratory Medicine, St. Joseph Mercy Hospital, Ann Arbor, Michigan (Dr Bartley).

出版信息

Arch Pathol Lab Med. 2017 May;141(5):658-665. doi: 10.5858/arpa.2016-0280-CP. Epub 2017 Mar 13.

Abstract

CONTEXT

  • With enormous growth in the field of molecular pathology, the reporting of results gleaned from this testing is essential to guide patient care.

OBJECTIVE

  • To examine molecular reports from laboratories participating in proficiency testing for required elements to convey molecular laboratory test results to clinicians and patients.

DESIGN

  • Molecular laboratories participating in the College of American Pathologists (CAP) proficiency testing program for BRAF mutation analysis were solicited to submit examples of final reports from 2 separate proficiency testing reporting cycles. Reports were reviewed for the presence or absence of relevant components.

RESULTS

  • A total of 107 evaluable reports were received (57 demonstrating a positive result for the BRAF V600E mutation and 50 negative). Methods for BRAF testing varied, with 95% (102 of 107) of reports adequately describing their assay methods and 87% (93 of 107) of reports adequately describing the target(s) of their assays. Information on the analytic sensitivity of the assay was present in 74% (79 of 107) of reports and 83% (89 of 107) reported at least 1 assay limitation, though only 34% (36 of 107) reported on variants not detected by their assays. Analytic and clinical interpretive comments were included in 99% (106 of 107) and 90% (96 of 107) of reports, respectively. Of participants that perform a laboratory-developed test, 88% (88 of 100) included language addressing the development of the assay.

CONCLUSIONS

  • Laboratories participating in BRAF proficiency testing through the CAP are including most of the required reporting elements to unambiguously convey molecular results. Laboratories should continue to strive to report these results in a concise and comprehensive manner.
摘要

背景

随着分子病理学领域的巨大发展,报告从该检测中获得的结果对于指导患者护理至关重要。

目的

检查参与能力验证的实验室的分子报告,以确定向临床医生和患者传达分子实验室检测结果所需的要素。

设计

邀请参与美国病理学家学会(CAP)BRAF突变分析能力验证计划的分子实验室提交两个独立能力验证报告周期的最终报告示例。对报告进行审查,看是否存在相关组成部分。

结果

共收到107份可评估报告(57份显示BRAF V600E突变呈阳性结果,50份呈阴性)。BRAF检测方法各不相同,95%(107份中的102份)的报告充分描述了其检测方法,87%(107份中的93份)的报告充分描述了其检测靶点。74%(107份中的79份)的报告包含了检测分析灵敏度的信息,83%(107份中的89份)报告了至少一项检测局限性,不过只有34%(107份中的36份)报告了其检测未检测到的变异。分析性和临床解释性评论分别包含在99%(107份中的106份)和90%(107份中的96份)的报告中。在进行实验室自行开发检测的参与者中,88%(100份中的88份)包含了有关检测方法开发的说明。

结论

通过CAP参与BRAF能力验证的实验室纳入了大多数明确传达分子结果所需的报告要素。实验室应继续努力以简洁和全面的方式报告这些结果。

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