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Screen-detected breast cancers have a lower mitotic activity index

机译:经筛查的乳腺癌的有丝分裂活性指数较低

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摘要

We know that screening for breast cancer leads to detection of smaller tumours with less lymph node metastases. Could it be possible that the decrease in mortality after screening is not only caused by this earlier stage, but also by a different mitotic activity index (MAI) of the tumours that are detected by screening? Is MAI a prognostic factor for recurrence-free survival? A retrospective study was carried out of 387 patients with breast cancer, treated at the University Hospital Nijmegen between January 1992 and September 1997. Ninety patients had screen-detected breast cancer, 297 patients had breast cancers detected outside the screening programme. The MAI, other prognostic factors and recurrence-free survival were determined. In non-screen-detected tumours the MAI is twice as high as in screen-detected tumours, even after correction for age took place. The MAI correlated well with other tumour characteristics. The MAI in itself is a prognostic factor for recurrence-free survival. Favourable outcome in screen detected breast cancer is not entirely caused by detecting cancer in early stages: quantitative features such as the MAI indicate a less malignant character of screen detected breast cancer. The MAI is an independent prognostic factor for recurrence-free survival. © 2000 Cancer Research Campaign
机译:我们知道,筛查乳腺癌可以检测到较小的肿瘤,且淋巴结转移较少。筛查后死亡率的降低是否可能不仅由该早期阶段引起,而且还由通过筛查发现的肿瘤的不同有丝分裂活性指数(MAI)引起? MAI是无复发生存的预后因素吗?回顾性研究对1992年1月至1997年9月在奈梅亨大学医院接受治疗的387例乳腺癌患者进行了回顾性研究。90例患者进行了筛查发现的乳腺癌,297例患者在筛查程序之外发现了乳腺癌。确定了MAI,其他预后因素和无复发生存率。在未进行筛查的肿瘤中,即使在校正年龄后,MAI仍是筛查的肿瘤的两倍。 MAI与其他肿瘤特征密切相关。 MAI本身是无复发生存的预后因素。筛查乳腺癌的良好结局并非完全由早期发现癌症引起:定量特征(例如MAI)表明筛查乳腺癌的恶性程度较低。 MAI是无复发生存的独立预后因素。 ©2000癌症研究运动

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