Breast Biomarker Cytology Practice in 2023: Results of a College of American Pathologists Survey.

Zaibo Li, Ann King, Rhona J Souers, Janie J Roberson, Shahla Masood, Deepu Alex, Martin J Magers, Poornima Hegde, Sana O Tabbara
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Abstract

Context.—: The College of American Pathologists (CAP) surveys provide national benchmarks of pathology practice.

Objective.—: To investigate breast biomarker cytology practice in domestic and international laboratories in 2023.

Design.—: We analyzed data from the CAP Breast Biomarker Cytology Practice Supplemental Questionnaire that was distributed to laboratories participating in the 2023 CAP Nongynecologic Cytopathology Education Program.

Results.—: Twenty-five percent (180 of 728) of responding laboratories routinely evaluated breast biomarkers in cytology specimens. Breast biomarkers evaluated in cytology specimens included estrogen receptor/progesterone receptor (98.9%; 175 of 177), human epidermal growth factor receptor 2 (HER2) (93.2%; 165 of 177), Ki-67 (48.6%; 86 of 177), programmed death ligand-1 (PD-L1) (20.9%; 37 of 177), and mismatch repair (19.8%; 35 of 177). Fine-needle aspiration was the most validated specimen type (85.3%; 133 of 156), followed by body fluids (82.1%; 128 of 156). All respondents validated cell blocks (100.0%; 165 of 165), with a few laboratories also validating cytospin slides (3.0%; 5 of 165), liquid-based slides (3.0%; 5 of 165), air-dried direct smears (2.4%; 4 of 165), and others. CytoLyt was the most used collection medium (55.4%; 87 of 157), followed by balanced salt solution (16.6%; 26 of 157), Roswell Park Memorial Institute Medium (13.4%; 21 of 157), and CytoRich Red (9.6%; 15 of 157). Almost all laboratories indicated routinely using formalin (90.4%; 151 of 167) as fixative, while a few laboratories used other types of fixative (ethanol [5.4%; 9 of 167], methanol [3.0%; 5 of 167]). Digital imaging platforms were used by only 12.9% (22 of 171) of responding laboratories. Forty-four laboratories (28.0%; 44 of 157) required cellularity adequacy for interpreting breast biomarkers on cytologic specimens. Additionally, some significant differences in breast biomarker testing practice were identified among different institution types and between domestic and international laboratories.

Conclusions.—: This is the first survey from the CAP to investigate breast biomarker cytology practices. The findings reveal some differences among institution types and between domestic and international laboratories. These data provide a baseline for and support further studies and/or guidelines to promote and refine these practices.

2023年乳腺生物标志物细胞学实践:美国病理学家调查学院的结果。
上下文。-:美国病理学家学会(CAP)的调查提供了病理学实践的国家基准。目的:探讨2023年国内外乳腺生物标志物细胞学研究现状。-:我们分析了来自CAP乳腺生物标志物细胞学实践补充问卷的数据,该问卷被分发给参加2023 CAP非妇科细胞病理学教育计划的实验室。25%的实验室(728个实验室中的180个)对细胞学标本中的乳腺生物标志物进行常规评估。细胞学标本中评估的乳腺生物标志物包括雌激素受体/孕激素受体(98.9%;175 / 177),人表皮生长因子受体2 (HER2) (93.2%;165 / 177), Ki-67 (48.6%;程序性死亡配体-1 (PD-L1) (20.9%;37 / 177),错配修复(19.8%;177个中的第35个)。细针穿刺是最有效的标本类型(85.3%;156人中有133人),其次是体液(82.1%;156页中的128页)。所有应答者都验证了细胞块(100.0%;165个中的165个),少数实验室也验证细胞自旋玻片(3.0%;165个中的5个),液体基载玻片(3.0%;165个中的5个),风干直接涂片(2.4%;165页中的4页),等等。CytoLyt是最常用的收集介质(55.4%);87 / 157),其次是平衡盐溶液(16.6%;罗斯威尔公园纪念学院中型(13.4%);157人中有21人),CytoRich Red (9.6%;157个中的15个)。几乎所有实验室都表示常规使用福尔马林(90.4%;167个实验室中的151个)作为固定剂,而少数实验室使用其他类型的固定剂(乙醇[5.4%;167个中的9个],甲醇[3.0%;[167])。只有12.9%(171个实验室中的22个)使用了数字成像平台。44个实验室(28.0%);157例中有44例要求细胞充分性来解释细胞学标本上的乳腺生物标志物。此外,不同机构类型和国内外实验室在乳腺生物标志物检测实践方面存在显著差异。-:这是CAP首次对乳腺生物标志物细胞学实践进行调查。研究结果揭示了机构类型之间以及国内和国际实验室之间的一些差异。这些数据为进一步研究和/或指导方针提供了基线,以促进和完善这些做法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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