Castells Xavier, Domingo Laia, Corominas Josep María, Torá-Rocamora Isabel, Quintana María Jesús, Baré Marisa, Vidal Carmen, Natal Carmen, Sánchez Mar, Saladié Francina, Ferrer Joana, Vernet Mar, Servitja Sonia, Rodríguez-Arana Ana, Roman Marta, Espinàs Josep Alfons, Sala María
Department of Epidemiology and Evaluation, IMIM (Hospital del Mar Medical Research Institute), Pg. Marítim 25-29, 08003, Barcelona, Catalonia, Spain,
Breast Cancer Res Treat. 2015 Jan;149(1):237-44. doi: 10.1007/s10549-014-3208-z. Epub 2014 Dec 13.
Benign breast disease increases the risk of breast cancer. This association has scarcely been evaluated in the context of breast cancer screening programs although it is a prevalent finding in mammography screening. We assessed the association of distinct categories of benign breast disease and subsequent risk of breast cancer, as well as the influence of a family history of breast cancer. A retrospective cohort study was conducted in 545,171 women aged 50-69 years biennially screened for breast cancer in Spain. The median of follow-up was 6.1 years. The age-adjusted rate ratio (RR) of breast cancer for women with benign breast disease, histologically classified into nonproliferative and proliferative disease with and without atypia, compared with women without benign breast disease was estimated by Poisson regression analysis. A stratified analysis by family history of breast cancer was performed in a subsample. All tests were two-sided. The age-adjusted RR of breast cancer after diagnosis of benign breast disease was 2.51 (95 % CI: 2.14-2.93) compared with women without benign breast disease. The risk was higher in women with proliferative disease with atypia (RR = 4.56, 95 % CI: 2.06-10.07) followed by those with proliferative disease without atypia (RR = 3.58; 95 % CI = 2.61-4.91). Women with nonproliferative disease and without a family history of breast cancer remained also at increased risk of cancer (OR = 2.23, 95 % CI: 1.86-2.68). An increased risk of breast cancer was observed among screening participants with proliferative or nonproliferative benign breast disease, regardless of a family history of breast cancer. This information may be useful to explore risk-based screening strategies.
良性乳腺疾病会增加患乳腺癌的风险。尽管这在乳腺钼靶筛查中是一个常见的发现,但在乳腺癌筛查项目的背景下,这种关联几乎没有得到评估。我们评估了不同类型的良性乳腺疾病与随后患乳腺癌风险之间的关联,以及乳腺癌家族史的影响。在西班牙对545171名年龄在50 - 69岁之间每两年接受一次乳腺癌筛查的女性进行了一项回顾性队列研究。随访的中位数为6.1年。通过泊松回归分析估计了组织学上分类为非增殖性和增殖性疾病(有或无异型性)的良性乳腺疾病女性与无良性乳腺疾病女性相比的年龄调整后乳腺癌发病率比(RR)。在一个子样本中进行了按乳腺癌家族史分层的分析。所有检验均为双侧检验。与无良性乳腺疾病的女性相比,诊断为良性乳腺疾病后的年龄调整后乳腺癌RR为2.51(95%CI:2.14 - 2.93)。异型性增殖性疾病女性的风险更高(RR = 4.56,95%CI:2.06 - 10.07),其次是无异型性增殖性疾病女性(RR = 3.58;95%CI = 2.61 - 4.91)。无增殖性疾病且无乳腺癌家族史的女性患癌风险也仍然增加(OR = 2.23,95%CI:1.86 - 2.68)。无论有无乳腺癌家族史,在患有增殖性或非增殖性良性乳腺疾病的筛查参与者中均观察到患乳腺癌风险增加。这些信息可能有助于探索基于风险的筛查策略。