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利用能力验证数据比较雌激素和孕激素受体抗体试剂

Comparison of Estrogen and Progesterone Receptor Antibody Reagents Using Proficiency Testing Data.

作者信息

Troxell Megan L, Long Thomas, Hornick Jason L, Ambaye Abiy B, Jensen Kristin C

出版信息

Arch Pathol Lab Med. 2017 Oct;141(10):1402-1412. doi: 10.5858/arpa.2016-0497-OA. Epub 2017 Jul 17.

Abstract

CONTEXT

  • Immunohistochemical analysis of estrogen receptor (ER) and progesterone receptor (PgR) expression in breast cancer is the current standard of care and directly determines therapy. In 2010 the American Society of Clinical Oncology and the College of American Pathologists (ASCO/CAP) published guidelines for ER and PgR predictive testing, encompassing preanalytic, analytic, postanalytic factors; antibody validation; and proficiency testing.

OBJECTIVE

  • To compare the performance of different antibody reagents for ER and PgR immunohistochemical analysis by using CAP proficiency testing data.

DESIGN

  • The CAP PM2 survey uses tissue microarrays of ten 2-mm cores per slide. We analyzed survey data from 80 ER and 80 PgR cores by antibody clone from more than 1200 laboratories.

RESULTS

  • Laboratories used the ER antibodies SP1 (72%), 6F11 (17%), 1D5 (3%), and the PgR antibodies 1E2 (61%), 16 (12%), PgR-636 (13%), PgR-1294 (8%) in 2015. While 63 of 80 ER cores (79%) were scored similarly using each of the 3 antibodies, there were significant differences for others, with SP1 yielding more positive interpretations. Four cores were scored as ER negative by more than half of the laboratories using 1D5 or 6F11, while SP1 produced positive results in more than 70% of laboratories using that antibody. Despite the greater variety of PgR antibody reagents and greater PgR tumor heterogeneity, 61 of 80 cores (76%) were scored similarly across the 4 PgR antibodies.

CONCLUSIONS

  • Accurate ER and PgR testing in breast cancer is crucial for appropriate treatment. The CAP proficiency testing data demonstrate differences in staining results by ER clone, with SP1 yielding more positive results.
摘要

背景

  • 乳腺癌中雌激素受体(ER)和孕激素受体(PgR)表达的免疫组织化学分析是当前的标准治疗手段,直接决定治疗方案。2010年,美国临床肿瘤学会和美国病理学家学会(ASCO/CAP)发布了ER和PgR预测性检测指南,涵盖分析前、分析和分析后因素;抗体验证;以及能力验证。

目的

  • 通过使用CAP能力验证数据,比较不同抗体试剂用于ER和PgR免疫组织化学分析的性能。

设计

  • CAP PM2调查使用每张载玻片上有十个2毫米芯的组织微阵列。我们分析了来自1200多个实验室的80个ER芯和80个PgR芯的调查数据,这些数据按抗体克隆分类。

结果

  • 2015年,实验室使用的ER抗体为SP1(72%)、6F11(17%)、1D5(3%),PgR抗体为1E2(61%)、16(12%)、PgR-636(13%)、PgR-1294(8%)。虽然80个ER芯中的63个(79%)使用这3种抗体中的每种进行评分时结果相似,但其他抗体存在显著差异,SP1产生的阳性解读更多。超过一半使用1D5或6F11的实验室将4个芯评为ER阴性,而使用SP1抗体的实验室中超过70%得出阳性结果。尽管PgR抗体试剂种类更多且PgR肿瘤异质性更大,但80个芯中的61个(76%)在4种PgR抗体之间的评分相似。

结论

  • 乳腺癌中准确的ER和PgR检测对于恰当治疗至关重要。CAP能力验证数据表明不同ER克隆的染色结果存在差异,SP1产生的阳性结果更多。

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