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免疫组织化学检测的分析验证:来自1085个实验室调查的新基准数据

Analytic Validation of Immunohistochemistry Assays: New Benchmark Data From a Survey of 1085 Laboratories.

作者信息

Stuart Lauren N, Volmar Keith E, Nowak Jan A, Fatheree Lisa A, Souers Rhona J, Fitzgibbons Patrick L, Goldsmith Jeffrey D, Astles J Rex, Nakhleh Raouf E

出版信息

Arch Pathol Lab Med. 2017 Sep;141(9):1255-1261. doi: 10.5858/arpa.2016-0559-CP. Epub 2017 May 30.

DOI:10.5858/arpa.2016-0559-CP
PMID:28557616
Abstract

CONTEXT

  • A cooperative agreement between the College of American Pathologists (CAP) and the United States Centers for Disease Control and Prevention was undertaken to measure laboratories' awareness and implementation of an evidence-based laboratory practice guideline (LPG) on immunohistochemical (IHC) validation practices published in 2014.

OBJECTIVE

  • To establish new benchmark data on IHC laboratory practices.

DESIGN

  • A 2015 survey on IHC assay validation practices was sent to laboratories subscribed to specific CAP proficiency testing programs and to additional nonsubscribing laboratories that perform IHC testing. Specific questions were designed to capture laboratory practices not addressed in a 2010 survey.

RESULTS

  • The analysis was based on responses from 1085 laboratories that perform IHC staining. Ninety-six percent (809 of 844) always documented validation of IHC assays. Sixty percent (648 of 1078) had separate procedures for predictive and nonpredictive markers, 42.7% (220 of 515) had procedures for laboratory-developed tests, 50% (349 of 697) had procedures for testing cytologic specimens, and 46.2% (363 of 785) had procedures for testing decalcified specimens. Minimum case numbers were specified by 85.9% (720 of 838) of laboratories for nonpredictive markers and 76% (584 of 768) for predictive markers. Median concordance requirements were 95% for both types. For initial validation, 75.4% (538 of 714) of laboratories adopted the 20-case minimum for nonpredictive markers and 45.9% (266 of 579) adopted the 40-case minimum for predictive markers as outlined in the 2014 LPG. The most common method for validation was correlation with morphology and expected results. Laboratories also reported which assay changes necessitated revalidation and their minimum case requirements.

CONCLUSIONS

  • Benchmark data on current IHC validation practices and procedures may help laboratories understand the issues and influence further refinement of LPG recommendations.
摘要

背景

美国病理学家学会(CAP)与美国疾病控制与预防中心达成合作协议,旨在评估实验室对2014年发布的关于免疫组织化学(IHC)验证实践的循证实验室实践指南(LPG)的认知和实施情况。

目的

建立关于免疫组织化学实验室实践的新基准数据。

设计

2015年,一项关于免疫组织化学检测验证实践的调查被发送至参与特定CAP能力验证计划的实验室,以及其他进行免疫组织化学检测的非参与实验室。特定问题旨在获取2010年调查中未涉及的实验室实践情况。

结果

分析基于1085家进行免疫组织化学染色的实验室的回复。96%(844家中的809家)总是记录免疫组织化学检测的验证情况。60%(1078家中的648家)对预测性和非预测性标志物有单独的程序,42.7%(515家中的220家)有实验室自建检测的程序,50%(697家中的349家)有检测细胞学标本的程序,46.2%(785家中的363家)有检测脱钙标本的程序。85.9%(838家中的720家)的实验室为非预测性标志物规定了最低病例数,76%(768家中的584家)为预测性标志物规定了最低病例数。两种类型的中位数一致性要求均为95%。对于初始验证,75.4%(714家中的538家)的实验室采用了2014年LPG中规定的非预测性标志物20例的最低要求,45.9%(579家中的266家)采用了预测性标志物40例的最低要求。最常见的验证方法是与形态学和预期结果进行相关性分析。实验室还报告了哪些检测变化需要重新验证以及它们的最低病例要求。

结论

关于当前免疫组织化学验证实践和程序的基准数据可能有助于实验室了解相关问题,并影响LPG建议的进一步完善。

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