Executive Vice Chair, Surgery; Associate Director, Samuel Oschin Comprehensive Cancer Institute, Cedars-Sinai Medical Center, Los Angeles, CA.
Professor of Pathology, Harvard Medical School, Beth Israel Deaconess Medical Center, Boston, MA.
CA Cancer J Clin. 2017 Jul 8;67(4):290-303. doi: 10.3322/caac.21393. Epub 2017 Mar 14.
Answer questions and earn CME/CNE The revision of the eighth edition of the primary tumor, lymph node, and metastasis (TNM) classification of the American Joint Commission of Cancer (AJCC) for breast cancer was determined by a multidisciplinary team of breast cancer experts. The panel recognized the need to incorporate biologic factors, such as tumor grade, proliferation rate, estrogen and progesterone receptor expression, human epidermal growth factor 2 (HER2) expression, and gene expression prognostic panels into the staging system. AJCC levels of evidence and guidelines for all tumor types were followed as much as possible. The panel felt that, to maintain worldwide value, the tumor staging system should remain based on TNM anatomic factors. However, the recognition of the prognostic influence of grade, hormone receptor expression, and HER2 amplification mandated their inclusion into the staging system. The value of commercially available, gene-based assays was acknowledged and prognostic input added. Tumor biomarkers and low Oncotype DX recurrence scores can alter prognosis and stage. These updates are expected to provide additional precision and flexibility to the staging system and were based on the extent of published information and analysis of large, as yet unpublished databases. The eighth edition of the AJCC TNM staging system, thus, provides a flexible platform for prognostic classification based on traditional anatomic factors, which can be modified and enhanced using patient biomarkers and multifactorial prognostic panel data. The eighth edition remains the worldwide basis for breast cancer staging and will incorporate future online updates to remain timely and relevant. CA Cancer J Clin 2017;67:290-303. © 2017 American Cancer Society.
回答问题并获得 CME/CNE 美国癌症联合委员会(AJCC)修订的第八版乳腺癌原发肿瘤、淋巴结和转移(TNM)分类是由一个多学科乳腺癌专家团队决定的。该小组认识到需要将生物学因素,如肿瘤分级、增殖率、雌激素和孕激素受体表达、人表皮生长因子 2(HER2)表达和基因表达预后小组纳入分期系统。尽可能遵循 AJCC 所有肿瘤类型的证据水平和指南。该小组认为,为了保持全球价值,肿瘤分期系统应继续基于 TNM 解剖因素。然而,分级、激素受体表达和 HER2 扩增的预后影响的认识要求将其纳入分期系统。商业上可用的基于基因的检测的价值得到了认可,并增加了预后输入。肿瘤生物标志物和低 Oncotype DX 复发评分可以改变预后和分期。这些更新有望为分期系统提供额外的准确性和灵活性,并且基于已发表信息的程度和对大型、尚未发表的数据库的分析。因此,第八版 AJCC TNM 分期系统为基于传统解剖因素的预后分类提供了一个灵活的平台,该平台可以使用患者生物标志物和多因素预后小组数据进行修改和增强。第八版仍然是全球乳腺癌分期的基础,并将纳入未来的在线更新,以保持及时和相关。CA Cancer J Clin 2017;67:290-303。©2017 美国癌症协会。