Department of Radiation Oncology, Institut Curie, Paris, France.
Department of Surgery, Institut Curie, Paris, France.
Br J Cancer. 2014 Apr 29;110(9):2195-200. doi: 10.1038/bjc.2014.143. Epub 2014 Apr 8.
The identification and validation of suitable predictive and prognostic factors are a challenge to improve the treatment scheme selection. Discordances in histological grade can be established between core biopsy and surgical specimens. This is important in HR-positive/HER2-negative subgroup where histological grade identifies patients at high risk and is a strong determinant for treatment scheme.
A total of 350 consecutive invasive breast carcinoma biopsies were assessed and compared with surgical specimens in Institut Curie, Paris, France. Clinical, radiological and pathological data were recorded.
Histological grade concordance rate in the HR+/HER2- group was 75%. A grade underestimation was mainly due to mitotic index misgrading (23%). Large tumours (P<0.05), premenopausal patients (P=0.005) and non-ultrasound-guided biopsies (P=0.04) were risk factors for misgrading. The highest discordance was found in tumours that required chemotherapy (39%, P<0.05), and it was related to an underestimation of histological grade on core biopsies (94%).
Histological grade in HR+/HER2- group is important to identify patients with poor prognosis and start a systemic therapy. Histological grade discordance was correlated with an underestimation of mitotic index and factors probably associated with intratumor heterogeneity (premenopausal status, tumour size and the type of core biopsy performed). But such discordance did not appear to modify the therapeutic decision, because systemic treatment decision-making also integrates other variables. Determining histological grade in core biopsy can be especially important in HR-positive/HER2-negative subgroup where it identifies patients at high risk and is a strong determinant of the treatment scheme.
识别和验证合适的预测和预后因素是改善治疗方案选择的挑战。核心活检和手术标本之间可能存在组织学分级的差异。这在 HR 阳性/HER2 阴性亚组中尤为重要,因为组织学分级确定了高危患者,是治疗方案的重要决定因素。
对法国巴黎居里研究所的 350 例连续浸润性乳腺癌活检进行评估,并与手术标本进行比较。记录临床、放射学和病理学数据。
HR+/HER2- 组的组织学分级一致性率为 75%。组织学分级低估主要是由于有丝分裂指数的错误分级(23%)。大肿瘤(P<0.05)、绝经前患者(P=0.005)和非超声引导活检(P=0.04)是错误分级的危险因素。在需要化疗的肿瘤中,分级差异最大(39%,P<0.05),这与核心活检中组织学分级的低估有关(94%)。
HR+/HER2- 组的组织学分级对于识别预后不良的患者并开始系统治疗很重要。组织学分级的差异与有丝分裂指数的低估以及可能与肿瘤内异质性相关的因素(绝经前状态、肿瘤大小和进行的核心活检类型)有关。但这种差异似乎并没有改变治疗决策,因为系统治疗决策还综合考虑了其他变量。在 HR 阳性/HER2 阴性亚组中,确定核心活检中的组织学分级尤为重要,因为它可以确定高危患者,是治疗方案的重要决定因素。