Counting of apoptotic cells: a methodological study in invasive breast cancer.

H A van de Schepop, J S de Jong, P J van Diest, J P Baak
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引用次数: 46

Abstract

Aims-To arrive at a reproducible sampling technique for counting apoptotic cells in tissue sections of invasive breast cancer that can serve as a protocol for further clinical studies.Methods-In 4 mum thick haematoxylin and eosin stained tissue sections of 12 breast cancers, apoptotic cells, recognised by strict morphological criteria, were counted in consecutive fields of vision at x1000 magnification in a marked area in the most poorly differentiated region of tumour. These counts were regarded as the gold standard. Subsequently, in a systematic sampling experiment, the number of fields that had to be counted to derive an acceptable coefficient of variation (CV) was determined. To compare counts at different magnifications, all fields of vision were also counted at x630 and x400. The intra- and inter-observer reproducibility was tested by repeated measurements at these magnifications in 10 systematically selected fields of vision.Results-Apoptosis seemed to be a rare event, affecting, on average, about 1% of tumour cells. Noticeable clustering of apoptotic cells was observed. The systematic sampling experiment showed that at x1000 magnification, the CV was improved by counting up to 20 fields. When comparing x400 and x630 magnifications with the x1000 magnification, the correlation coefficients were 0.88 and 0.87, respectively. However, the lower magnifications yielded lower counts. With regard to reproducibility, the intra-observer correlation coefficient was 0.91 at x630 and 0.76 at x400. The inter-observer correlation coefficient was 0.77 at x630 and 0.68 at x400.Conclusions-Apoptotic cells can be counted readily in haematoxylin and eosin stained tissue sections. However, a systematic sampling protocol must be followed and cells should be counted at a relatively high magnification to obtain acceptable reproducibility. The suggested protocol will permit further correlative and prognostic studies and the monitoring of the effects of treatment.

凋亡细胞计数:浸润性乳腺癌的方法学研究。
目的:研究浸润性乳腺癌组织切片中凋亡细胞计数的可重复采样技术,为进一步的临床研究提供参考。方法:在12例乳腺癌的4张厚的苏木精和伊红染色的组织切片中,在肿瘤最低分化区域的标记区域连续视野中,在x1000倍放大镜下计数凋亡细胞,这些细胞符合严格的形态学标准。这些数据被视为黄金标准。随后,在系统抽样实验中,确定了必须计数以得出可接受的变异系数(CV)的田的数量。为了比较不同倍率下的计数,所有视野也在x630和x400下计数。通过在10个系统选择的视野中重复测量这些放大率来测试观察者内部和观察者之间的可重复性。结果:细胞凋亡似乎是一个罕见的事件,平均影响约1%的肿瘤细胞。凋亡细胞明显聚集。系统采样实验表明,在x1000的放大倍数下,CV可以计数到20个场。将x400、x630放大倍数与x1000放大倍数进行比较,相关系数分别为0.88和0.87。然而,较低的放大倍率产生较低的计数。在再现性方面,x630和x400的观察者内相关系数分别为0.91和0.76。观察者间相关系数在x630为0.77,在x400为0.68。结论:在苏木精染色和伊红染色的组织切片上可以很容易地计数到凋亡细胞。但是,必须遵循系统的采样方案,并且应该在相对较高的倍率下计数细胞,以获得可接受的再现性。建议的方案将允许进一步的相关和预后研究以及治疗效果的监测。
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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