Reinisch Mattea, Huober Jens, von Minckwitz Gunter, Blohmer Jens-Uwe, Denkert Carsten, Hanusch Claus, Jackisch Christian, Kümmel Sherko, Schneeweiss Andreas, Rhiem Kerstin, Lederer Bianca, Untch Michael, Nekljudova V Valentina, Loibl Sibylle
Breast Unit, Kliniken-Essen-Mitte, Henricistrasse 92, 45138 Essen, Germany.
Department of Obstetrics and Gynaecology, Universitätsfrauenklinik Ulm, Prittwitzstrasse 43, 89075 Ulm, Germany.
Breast. 2017 Apr;32:73-78. doi: 10.1016/j.breast.2016.12.020. Epub 2017 Jan 5.
Patients with bilateral breast cancer (BBC) are usually excluded from participating in clinical trials and little is known about the response and outcome of BBC to neoadjuvant chemotherapy compared to unilateral BC (UBC).
We prospectively captured the information on patients with BBC in our database treated within four neoadjuvant chemotherapy trials and collected retrospectively the rate of pathological complete response (pCR) defined as ypT0 ypN0, ypT0/is ypN0, ypT0 ypNX, clinical and histologic parameters. Synchronous carcinoma in the contralateral breast was considered as the non-indicator lesion. Patients with UBC only treated within the same neoadjuvant trials performed the control group.
From the 6727 patients treated within 4 German neoadjuvant trials 119 (1.8%) patients have been identified with the diagnosis of BBC. The pCR rate (ypT0 ypN0) was 12.6% in the non-indicator lesion group versus 10.9% the indicator lesion group versus 20.9% for patients with unilateral disease (p = 0.003). There were more advanced tumor stages and positive axillary lymph nodes in the indicator lesion than in the nonindicator lesion or in UBC. In 52.5% the molecular subtype was identical between indicator and non-indicator lesion with more triple negative and HER2 positive BC in the group of UBC. The disease free survival rate (DFS) was 25.8% for patients with UBC versus 39.6% for patients with BBC.
The selection for the indicator lesion was based on tumor size, nodal status and inclusion criteria. Patients with BBC patients had a lower pCR rate and a lower DFS.
双侧乳腺癌(BBC)患者通常被排除在临床试验之外,与单侧乳腺癌(UBC)相比,关于BBC对新辅助化疗的反应和结果知之甚少。
我们前瞻性地收集了在四项新辅助化疗试验中接受治疗的BBC患者的信息,并回顾性收集了病理完全缓解(pCR)率,定义为ypT0 ypN0、ypT0/is ypN0、ypT0 ypNX、临床和组织学参数。对侧乳房的同步癌被视为非指示性病变。仅在相同新辅助试验中接受治疗的UBC患者作为对照组。
在德国的4项新辅助试验中治疗的6727例患者中,有119例(1.8%)被诊断为BBC。非指示性病变组的pCR率(ypT0 ypN0)为12.6%,指示性病变组为10.9%,单侧疾病患者为20.9%(p = 0.003)。指示性病变中的肿瘤分期更晚,腋窝淋巴结阳性率高于非指示性病变或UBC。52.5%的指示性和非指示性病变分子亚型相同,UBC组中三阴性和HER2阳性乳腺癌更多。UBC患者的无病生存率(DFS)为25.8%,而BBC患者为39.6%。
指示性病变的选择基于肿瘤大小、淋巴结状态和纳入标准。BBC患者的pCR率和DFS较低。