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激素受体阳性乳腺癌的病因因组织学分级和增殖水平而异。

Etiology of hormone receptor positive breast cancer differs by levels of histologic grade and proliferation.

机构信息

Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Rockville, MD.

Division of Genetics and Epidemiology, The Institute of Cancer Research, London, United Kingdom.

出版信息

Int J Cancer. 2018 Aug 15;143(4):746-757. doi: 10.1002/ijc.31352. Epub 2018 Mar 25.

Abstract

Limited epidemiological evidence suggests that the etiology of hormone receptor positive (HR+) breast cancer may differ by levels of histologic grade and proliferation. We pooled risk factor and pathology data on 5,905 HR+ breast cancer cases and 26,281 controls from 11 epidemiological studies. Proliferation was determined by centralized automated measures of KI67 in tissue microarrays. Odds ratios (OR), 95% confidence intervals (CI) and p-values for case-case and case-control comparisons for risk factors in relation to levels of grade and quartiles (Q1-Q4) of KI67 were estimated using polytomous logistic regression models. Case-case comparisons showed associations between nulliparity and high KI67 [OR (95% CI) for Q4 vs. Q1 = 1.54 (1.22, 1.95)]; obesity and high grade [grade 3 vs. 1 = 1.68 (1.31, 2.16)] and current use of combined hormone therapy (HT) and low grade [grade 3 vs. 1 = 0.27 (0.16, 0.44)] tumors. In case-control comparisons, nulliparity was associated with elevated risk of tumors with high but not low levels of proliferation [1.43 (1.14, 1.81) for KI67 Q4 vs. 0.83 (0.60, 1.14) for KI67 Q1]; obesity among women ≥50 years with high but not low grade tumors [1.55 (1.17, 2.06) for grade 3 vs. 0.88 (0.66, 1.16) for grade 1] and HT with low but not high grade tumors [3.07 (2.22, 4.23) for grade 1 vs. 0.85 (0.55, 1.30) for grade 3]. Menarcheal age and family history were similarly associated with HR+ tumors of different grade or KI67 levels. These findings provide insights into the etiologic heterogeneity of HR+ tumors.

摘要

有限的流行病学证据表明,激素受体阳性(HR+)乳腺癌的病因可能因组织学分级和增殖水平而异。我们汇集了 11 项流行病学研究中 5905 例 HR+乳腺癌病例和 26281 例对照的危险因素和病理学数据。增殖通过组织微阵列中 Ki67 的集中自动化测量来确定。使用多分类逻辑回归模型,针对危险因素与分级和 Ki67 四分位数(Q1-Q4)水平之间的病例-病例和病例对照比较,估计了等级和四分位数(Q1-Q4)的比值比(OR)、95%置信区间(CI)和 p 值。病例-病例比较显示,未婚与 Ki67 高[四分位距(Q4)与 Q1 的比值比(95%CI)为 1.54(1.22, 1.95)]、肥胖与高级别[级别 3 与 1=1.68(1.31, 2.16)]和当前使用联合激素治疗(HT)与低级别[级别 3 与 1=0.27(0.16, 0.44)]肿瘤之间存在关联。在病例对照比较中,未婚与高但不是低增殖水平的肿瘤风险升高相关[Ki67 Q4 与 Ki67 Q1 的比值比(OR)为 1.43(1.14, 1.81)];≥50 岁女性中肥胖与高级别但不是低级别肿瘤相关[级别 3 与级别 1 的比值比(OR)为 1.55(1.17, 2.06)],而 HT 与低级别但不是高级别肿瘤相关[级别 1 的比值比(OR)为 3.07(2.22, 4.23)]与级别 3 的 0.85(0.55, 1.30)]。初潮年龄和家族史也与不同分级或 Ki67 水平的 HR+肿瘤具有相似的相关性。这些发现为 HR+肿瘤的病因异质性提供了深入了解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c45/6120057/2fea3692c052/IJC-143-746-g001.jpg

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