Mao Kai, Yang Yaping, Wu Wei, Liang Shi, Deng Heran, Liu Jieqiong
Guangdong Provincial Key Laboratory of Malignant Tumor Epigenetics and Gene Regulation, Department of General Surgery, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou, China.
Guangdong Provincial Key Laboratory of Malignant Tumor Epigenetics and Gene Regulation, Department of Breast Surgery, Breast Tumor Center, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou, China.
PLoS One. 2017 May 3;12(5):e0176417. doi: 10.1371/journal.pone.0176417. eCollection 2017.
Although subsequent breast cancer risk after primary lobular carcinoma in situ (LCIS) has been studied intensively, whether the risk of second breast cancer after first LCIS varies with hormone receptor (HR) status of primary tumor remains unclear.
We identified 10,304 women with primary pure unilateral LCIS between 1998 and 2007 from the Surveillance, Epidemiology and End Results (SEER) 18 Registries. Kaplan-Meier estimates of 5 or 10-year probabilities of second ipsilateral breast cancers (IBCs) and contralateral breast cancers (CBCs) were calculated. Multivariable Cox proportional model was performed to identify impact of HR status of primary LCIS, and other demographic, clinicopathologic or treatment characteristics on risk of second IBCs or CBCs.
Of the 10,304 women with primary LCIS included in this study, 9949 (96.5%) patients had HR+ tumors, and 355 (3.5%) had HR- tumors. Multivariable-adjusted analyses showed that although there was no difference in risk of total second IBCs between women with HR+ and HR- LCIS (P = 0.152), patients with HR+ LCIS had a statistically lower risk of second invasive IBCs compared to those with HR- LCIS (hazard ratio 0.356, 95% CI 0.141-0.899, P = 0.029). Women with primary HR+ LCIS had lower risks of both second total and invasive CBCs compared to those with HR- LCIS (total CBCs: hazard ratio 0.340, 95% CI 0.228-0.509, P<0.001; invasive CBCs: hazard ratio 0.172, 95% CI 0.108-0.274, P<0.001). Additionally, black women had a 2-fold risk of developing subsequent total IBCs than white women (P = 0.028).
This population-based study demonstrated that the risk of second breast cancers was significantly increased in women with HR- first LCIS compared to those with HR+ LCIS. These findings warrant intensive surveillance for second breast cancers in HR- LCIS survivors.
尽管原发性小叶原位癌(LCIS)后发生后续乳腺癌的风险已得到深入研究,但首次LCIS后发生第二原发性乳腺癌的风险是否因原发性肿瘤的激素受体(HR)状态而异仍不清楚。
我们从监测、流行病学和最终结果(SEER)18个登记处中识别出1998年至2007年间患有原发性单纯单侧LCIS的10304名女性。计算了同侧第二原发性乳腺癌(IBC)和对侧第二原发性乳腺癌(CBC)的5年或10年发生概率的Kaplan-Meier估计值。采用多变量Cox比例模型来确定原发性LCIS的HR状态以及其他人口统计学、临床病理或治疗特征对第二原发性IBC或CBC风险的影响。
在本研究纳入的10304名患有原发性LCIS的女性中,9949名(96.5%)患者的肿瘤为HR阳性,355名(3.5%)患者的肿瘤为HR阴性。多变量调整分析显示,尽管HR阳性和HR阴性LCIS女性的第二原发性IBC总体风险没有差异(P = 0.152),但与HR阴性LCIS患者相比,HR阳性LCIS患者发生第二原发性浸润性IBC的风险在统计学上较低(风险比0.356,95%置信区间0.141 - 0.899,P = 0.029)。与HR阴性LCIS患者相比,原发性HR阳性LCIS女性发生第二原发性CBC总体和浸润性CBC的风险均较低(总体CBC:风险比0.340,95%置信区间0.228 - 0.509,P<0.001;浸润性CBC:风险比0.172,95%置信区间0.108 - 0.274,P<0.001)。此外,黑人女性发生后续总体IBC的风险是白人女性的2倍(P = 0.028)。
这项基于人群的研究表明,与HR阳性LCIS女性相比,HR阴性首次LCIS女性发生第二原发性乳腺癌的风险显著增加。这些发现值得对HR阴性LCIS幸存者进行第二原发性乳腺癌的强化监测。