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首页> 外文期刊>British Journal of Cancer >Established breast cancer risk factors by clinically important tumour characteristics
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Established breast cancer risk factors by clinically important tumour characteristics

机译:通过临床重要的肿瘤特征确定乳腺癌危险因素

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Breast cancer is a morphologically and clinically heterogeneous disease; however, it is less clear how risk factors relate to tumour features. We evaluated risk factors by tumour characteristics (histopathologic type, grade, size, and nodal status) in a population-based case–control of 2386 breast cancers and 2502 controls in Poland. Use of a novel extension of the polytomous logistic regression permitted simultaneous modelling of multiple tumour characteristics. Late age at first full-term birth was associated with increased risk of large (>2?cm) tumours (odds ratios (95% confidence intervals) 1.19 (1.07–1.33) for a 5-year increase in age), but not smaller tumours (P for heterogeneity adjusting for other tumour features (Phet)=0.007). On the other hand, multiparity was associated with reduced risk for small tumours (0.76 (0.68–0.86) per additional birth; Phet=0.004). Consideration of all tumour characteristics simultaneously revealed that current or recent use of combined hormone replacement therapy was associated with risk of small (2.29 (1.66–3.15)) and grade 1 (3.36 (2.22–5.08)) tumours (Phet=0.05 for size and 0.0008 for grade 1 vs 3), rather than specific histopathologic types (Phet=0.63 for ductal vs lobular). Finally, elevated body mass index was associated with larger tumour size among both pre- and postmenopausal women (Phet=0.05 and 0.0001, respectively). None of these relationships were explained by hormone receptor status of the tumours. In conclusion, these data support distinctive risk factor relationships by tumour characteristics of prognostic relevance. These findings might be useful in developing targeted prevention efforts.
机译:乳腺癌是一种形态和临床上异质的疾病。但是,尚不清楚危险因素与肿瘤特征之间的关系。我们以人群为基础的病例对照(波兰的2386例乳腺癌和2502例对照)中的肿瘤特征(组织病理学类型,等级,大小和淋巴结状态)评估了危险因素。多态性逻辑回归的新型扩展的使用允许同时建模多个肿瘤特征。初次足月出生的晚年龄与大(> 2?cm)肿瘤的风险增加相关(奇数比(95%置信区间),年龄增加5年的比率为1.19(1.07–1.33)),但并非如此较小的肿瘤(P用于异质性调整其他肿瘤特征(Phet)= 0.007)。另一方面,多胎性与小肿瘤风险降低相关(每增加一胎生育0.76(0.68–0.86); Phet = 0.004)。同时考虑所有肿瘤特征表明,目前或最近使用联合激素替代疗法与小(2.29(1.66–3.15))和1级(3.36(2.22–5.08))肿瘤(大小和Phet = 0.05)的风险有关。 1级对3级为0.0008),而不是特定的组织病理学类型(导管对小叶为Phet = 0.63)。最后,在绝经前和绝经后妇女中,体重指数升高与更大的肿瘤大小相关(分别为Phet = 0.05和0.0001)。这些关系均不能通过肿瘤的激素受体状态来解释。总之,这些数据通过预后相关的肿瘤特征支持了独特的危险因素关系。这些发现可能有助于开展有针对性的预防工作。

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