Braun Michael, Kriegmair Antonia, Szeterlak Nina, Andrulat Anne, Schrodi Simone, Kriner Monika, Hanusch Claus, Hamann Moritz, Stoetzer Oliver, Pölcher Martin
Department of Gynecology, Breast Center, Red Cross Hospital, Munich, Germany.
Munich Cancer Registry (MCR) at the Institute of Medical Information Processing, Biometry and Epidemiology (IBE), LMU Munich, Regional Centre Munich, Bavarian Cancer Registry, Bavarian Health and Food Safety Authority (LGL), Munich, Germany.
Breast Care (Basel). 2022 Jun;17(3):288-295. doi: 10.1159/000521096. Epub 2021 Nov 26.
The aim of the present study was to analyze the performance of Oncotype DX® multigene assay (ODX®) in patients with 0-3 lymph nodes in a high-volume community hospital.
Patients with non-metastatic HR*/HER2- EBC and 0-3 positive lymph nodes, who underwent primary surgery at the Red Cross Hospital Munich, Germany and consecutively had ODX® testing were included in this retrospective study. The distribution of clinicopathologic characteristics, recurrence score (RS) risk, and use of systemic therapy were compared among patients without positive lymph nodes (N0) and patients with micrometastases or 1 to 3 positive lymph nodes (N1). Disease-free survival (DFS) and overall survival (OS) were estimated.
From 2012 to 2017 ODX® was consecutively performed in 575 (16.4%) of 3,492 women with HR*/HER- EBC, of which 553 were eligible for this analysis (N0: 60.8%; N1: 39.2%). Among the patients included, 441 (79.7%) had an RS of 0 to 25 and 112 (20.3%) had an RS of 26 or higher. In patients with RS 0 to 25 the rate of chemotherapy use was low, independent from nodal status (N0: 17.1% and N1: 19.1%) and 5-year DFS was 90.5% and 91.7% for N0 and N1 patients, respectively. There was no significant difference in DFS (90.5% vs. 93.3%; = 0.101) or OS (97.2% vs. 96.0%; = 0.737) for patients with an RS of 0 to 25 when treated with chemo-endocrine therapy or endocrine therapy alone, independent from nodal status.
The results of the study confirm the observations from randomized studies on the use of the ODX® in a real-world population in terms of risk distribution and patient outcome. Adjuvant chemotherapy could be safely omitted in patients with HR*/HER2- breast cancer with 0-3 positive lymph nodes and RS <25.
本研究的目的是分析在一家大型社区医院中,Oncotype DX®多基因检测(ODX®)在0至3个淋巴结转移患者中的表现。
本回顾性研究纳入了在德国慕尼黑红十字医院接受初次手术且连续进行ODX®检测的非转移性HR*/HER2-早期乳腺癌(EBC)且有0至3个阳性淋巴结的患者。比较了无阳性淋巴结(N0)患者与有微转移或1至3个阳性淋巴结(N1)患者的临床病理特征分布、复发评分(RS)风险及全身治疗的使用情况。评估了无病生存期(DFS)和总生存期(OS)。
2012年至2017年期间,在3492例HR*/HER-EBC女性患者中,有575例(16.4%)连续进行了ODX®检测,其中553例符合本分析条件(N0:60.8%;N1:39.2%)。在纳入的患者中,441例(79.7%)的RS为0至25,112例(20.3%)的RS为26或更高。RS为0至25的患者中,化疗使用率较低,与淋巴结状态无关(N0:17.1%,N1:19.1%),N0和N1患者的5年DFS分别为90.5%和91.7%。RS为0至25的患者接受化疗联合内分泌治疗或单纯内分泌治疗时,DFS(90.5%对93.3%;P = 0.101)或OS(97.2%对96.0%;P = 0.737)无显著差异,与淋巴结状态无关。
本研究结果证实了随机研究中关于ODX®在真实世界人群中的使用在风险分布和患者预后方面的观察结果。对于有0至3个阳性淋巴结且RS<25的HR*/HER2-乳腺癌患者,可以安全地省略辅助化疗。