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Mitosis detection in breast cancer histological images An ICPR 2012 contest

机译:乳腺癌组织学图像中的有丝分裂检测ICPR 2012竞赛

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Introduction:In the framework of the Cognitive Microscope (MICO) project, we have set up a contest about mitosis detection in images of H and E stained slides of breast cancer for the conference ICPR 2012. Mitotic count is an important parameter for the prognosis of breast cancer. However, mitosis detection in digital histopathology is a challenging problem that needs a deeper study. Indeed, mitosis detection is difficult because mitosis are small objects with a large variety of shapes, and they can thus be easily confused with some other objects or artefacts present in the image. We added a further dimension to the contest by using two different slide scanners having different resolutions and producing red-green-blue (RGB) images, and a multi-spectral microscope producing images in 10 different spectral bands and 17 layers Z-stack. 17 teams participated in the study and the best team achieved a recall rate of 0.7 and precision of 0.89.Context:Several studies on automatic tools to process digitized slides have been reported focusing mainly on nuclei or tubule detection. Mitosis detection is a challenging problem that has not yet been addressed well in the literature.Aims:Mitotic count is an important parameter in breast cancer grading as it gives an evaluation of the aggressiveness of the tumor. However, consistency, reproducibility and agreement on mitotic count for the same slide can vary largely among pathologists. An automatic tool for this task may help for reaching a better consistency, and at the same time reducing the burden of this demanding task for the pathologists.Subjects and Methods:Professor Frιdιrique Capron team of the pathology department at Pitiι-Salpκtriθre Hospital in Paris, France, has selected a set of five slides of breast cancer. The slides are stained with H and E. They have been scanned by three different equipments: Aperio ScanScope XT slide scanner, Hamamatsu NanoZoomer 2.0-HT slide scanner and 10 bands multispectral microscope. The data set is made up of 50 high power fields (HPF) coming from 5 different slides scanned at ×40 magnification. There are 10 HPFs/slide. The pathologist has annotated all the mitotic cells manually. A HPF has a size of 512 μm × 512 μm (that is an area of 0.262 mm 2 , which is a surface equivalent to that of a microscope field diameter of 0.58 mm. These 50 HPFs contain a total of 326 mitotic cells on images of both scanners, and 322 mitotic cells on the multispectral microscope.Results:Up to 129 teams have registered to the contest. However, only 17 teams submitted their detection of mitotic cells. The performance of the best team is very promising, with F-measure as high as 0.78. However, the database we provided is by far too small for a good assessment of reliability and robustness of the proposed algorithms.Conclusions:Mitotic count is an important criterion in the grading of many types of cancers, however, very little research has been made on automatic mitotic cell detection, mainly because of a lack of available data. A main objective of this contest was to propose a database of mitotic cells on digitized breast cancer histopathology slides to initiate works on automated mitotic cell detection. In the future, we would like to extend this database to have much more images from different patients and also for different types of cancers. In addition, mitotic cells should be annotated by several pathologists to reflect the partial agreement among them.
机译:简介:在认知显微镜(MICO)项目的框架内,我们为ICPR 2012大会举​​办了有关在H和E染色的乳腺癌玻片图像中进行有丝分裂检测的竞赛。有丝分裂计数是预后的重要参数乳腺癌。但是,数字组织病理学中的有丝分裂检测是一个具有挑战性的问题,需要更深入的研究。确实,有丝分裂的检测是困难的,因为有丝分裂是具有多种形状的小物体,因此它们很容易与图像中存在的其他物体或伪像混淆。我们通过使用两个具有不同分辨率并产生红绿蓝(RGB)图像的不同幻灯片扫描仪,以及一个在10个不同光谱带和17层Z堆栈中产生图像的多光谱显微镜,为比赛增加了一个新的维度。 17个团队参加了这项研究,最好的团队实现了0.7的查全率和0.89的查准率。背景:据报道,对处理数字化载玻片的自动工具进行了多次研究,这些研究主要集中在核或肾小管的检测上。有丝分裂检测是一个尚未在文献中得到很好解决的具有挑战性的问题。目的:有丝分裂计数是乳腺癌分级中的重要参数,因为它可以评估肿瘤的侵袭性。但是,对于同一玻片,一致性,可重复性和有丝分裂计数的一致性在病理学家之间可能会有很大差异。自动执行此任务的工具可能有助于达到更好的一致性,同时减轻病理学家的这项艰巨任务的负担。对象和方法:巴黎皮蒂-萨尔普克三塔雷医院病理科的FrιdιriqueCapron教授团队,法国选择了一组五种乳腺癌切片。载玻片用H和E染色。它们已通过三种不同的设备进行了扫描:Aperio ScanScope XT载玻片扫描仪,Hamamatsu NanoZoomer 2.0-HT载玻片扫描仪和10波段多光谱显微镜。数据集由来自50个高功率场(HPF)组成,它们来自5张不同的幻灯片,放大倍数为40倍。每张幻灯片有10个HPF。病理学家手动注释了所有有丝分裂细胞。 HPF的大小为512μm×512μm(即0.262 mm 2的面积,其表面等效于显微镜视场直径的0.58 mm。这50个HPF包含326个有丝分裂细胞)结果:多达129个团队报名参加了比赛,但是只有17个团队提交了有丝分裂细胞的检测结果,最好的团队的表现非常乐观,采用F-measure结论:有丝分裂计数是许多类型癌症分级中的重要标准,但是有丝分裂计数是高达0.78的很好的评估标准。这项研究的主要目的是在数字化乳腺癌组织病理学幻灯片上建立一个有丝分裂细胞数据库,以启动有关自动mit的工作。耳细胞检测。将来,我们希望扩展该数据库,以提供更多来自不同患者以及不同类型癌症的图像。另外,有丝分裂细胞应由几位病理学家标注,以反映它们之间的部分一致性。

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