Research Unit in Medical Senology, Department of Medicine, European Institute of Oncology, Milan, Italy.
Clin Breast Cancer. 2013 Apr;13(2):95-102. doi: 10.1016/j.clbc.2012.11.004. Epub 2012 Dec 14.
Conflicting data are available in the literature on the outcome of invasive apocrine carcinoma (IAC), possibly related to a heterogeneous classification of these tumors.
A series of 6899 consecutive patients with invasive ductal carcinoma (IDC) not otherwise specified and 72 patients with immunohistochemically defined IAC who received surgery at the European Institute of Oncology between 1997 and 2005 were included. We then explored patterns of recurrence of IAC according to 2 immunohistochemically defined tumor subtypes: pure apocrine carcinoma (estrogen [ER] and progesterone [PgR] receptor negative, and AR positive) and apocrine-like carcinoma (ER or PgR positive and AR negative).
The diagnosis of pure apocrine carcinoma was correlated with a worse outcome in terms of DFS (hazard ratio [HR] 1.7; 95% confidence interval [CI], 1.01-2.86; P = .0010) if compared with IDC, whereas IDC and apocrine-like breast cancers showed a similar outcome in terms of DFS and overall survival. Patients with pure apocrine carcinoma had an increased risk in contralateral breast cancer (HR, 4.12; 95% CI, 1.22-14; P = .02).
Pure apocrine carcinoma represents a distinct subtype of breast cancer with a significantly worse DFS as compared with IDC. AR determination might have an important prognostic implication in IAC. Moreover, AR-targeted therapy should be further explored within these tumors.
关于浸润性大汗腺癌(IAC)的结局,文献中存在相互矛盾的数据,这可能与这些肿瘤的异质性分类有关。
本研究纳入了 1997 年至 2005 年期间在欧洲肿瘤研究所接受手术治疗的 6899 例未特指浸润性导管癌(IDC)患者和 72 例经免疫组织化学定义为 IAC 的患者。然后,我们根据 2 种免疫组织化学定义的肿瘤亚型探索了 IAC 的复发模式:纯大汗腺癌(雌激素[ER]和孕激素[PgR]受体阴性,AR 阳性)和大汗腺癌样癌(ER 或 PgR 阳性,AR 阴性)。
与 IDC 相比,纯大汗腺癌的诊断与 DFS(风险比[HR]1.7;95%置信区间[CI],1.01-2.86;P=0.0010)较差相关,而 IDC 和大汗腺癌样乳腺癌在 DFS 和总生存方面具有相似的结局。纯大汗腺癌患者发生对侧乳腺癌的风险增加(HR,4.12;95%CI,1.22-14;P=0.02)。
纯大汗腺癌是一种独特的乳腺癌亚型,与 IDC 相比,DFS 明显较差。AR 检测可能对 IAC 具有重要的预后意义。此外,应进一步探讨针对这些肿瘤的 AR 靶向治疗。