Aydiner Adnan, Sen Fatma, Tambas Makbule, Ciftci Rumeysa, Eralp Yesim, Saip Pinar, Karanlik Hasan, Fayda Merdan, Kucucuk Seden, Onder Semen, Yavuz Ekrem, Muslumanoglu Mahmut, Igci Abdullah
From the Department of Medical Oncology (AA, FS, RC, YE, PS); Department of Radiation Oncology (MT, MF, SK); Surgical Oncology Unit, Institute of Oncology (HK); Department of Pathology (SO, EY); and Surgical Oncology Unit, Istanbul Faculty of Medicine, Istanbul University, Istanbul, Turkey (MM, AI).
Medicine (Baltimore). 2015 Dec;94(52):e2341. doi: 10.1097/MD.0000000000002341.
Metaplastic breast carcinoma (MBC) differs from classic invasive ductal carcinomas regarding incidence, pathogenesis, and prognosis. The purpose of this study was to compare patients with MBC with clinicopathologic and treatment-matched patients with triple-negative breast carcinoma (TNBC) in terms of response to treatment, progression, and survival.Fifty-four patients with MBC and 51 with TNBC, who were treated at Istanbul University, Institute of Oncology, between 1993 and 2014, were included in the study. After correctly matching the patients with 1 of the 2 groups, they were compared to determine differences in response to treatment, disease progression, clinical course, and survival.At a median follow-up of 28 months, 18 patients (17.1%) died and 27 (25.5%) had disease progression. Metaplastic histology was significantly correlated with worse 3-year progression-free survival (PFS) (51 ± 9% vs. 82 ± 6%, P = 0.013) and overall survival (OS) (68 ± 8% vs. 94 ± 4%, P = 0.009) compared with TNBC histology. Patients who received taxane-based chemotherapy (CT) regimens or adjuvant radiotherapy had significantly better PFS (P = 0.002 and P < 0.001) and OS (P < 0.001 and P < 0.001) compared with others. In the multivariate analysis, MBC (hazard ratio [HR]: 0.09, P < 0.001), presence of neoadjuvant chemotherapy (NACT) (HR: 12.8, P = 0.05), and metastasis development at any time during the clinical course (HR: 38.7, P < 0.001) were significant factors that decreased PFS, whereas metastasis development was the only independent prognostic factor of OS (HR: 23.8, P = 0.009).MBC is significantly correlated with worse PFS and OS compared with TNBC. Patients with MBC are resistant to conventional CT agents, and more efficient treatment regimens are required.
化生性乳腺癌(MBC)在发病率、发病机制和预后方面与经典浸润性导管癌不同。本研究的目的是比较MBC患者与临床病理特征匹配且治疗方案匹配的三阴性乳腺癌(TNBC)患者在治疗反应、疾病进展和生存方面的差异。本研究纳入了1993年至2014年期间在伊斯坦布尔大学肿瘤研究所接受治疗的54例MBC患者和51例TNBC患者。在将患者正确匹配到两组中的一组后,对他们进行比较,以确定治疗反应、疾病进展、临床病程和生存方面的差异。中位随访28个月时,18例患者(17.1%)死亡,27例患者(25.5%)出现疾病进展。与TNBC组织学相比,化生性组织学与更差的3年无进展生存期(PFS)(51±9%对82±6%,P = 0.013)和总生存期(OS)(68±8%对94±4%,P = 0.009)显著相关。接受紫杉烷类化疗(CT)方案或辅助放疗的患者与其他患者相比,PFS(P = 0.002和P < 0.001)和OS(P < 0.001和P < 0.001)显著更好。在多变量分析中,MBC(风险比[HR]:0.09,P < 0.001)、新辅助化疗(NACT)的存在(HR:12.8,P = 0.05)以及临床病程中任何时间出现转移(HR:38.7,P < 0.001)是降低PFS的显著因素,而转移的发生是OS的唯一独立预后因素(HR:23.8,P = 0.009)。与TNBC相比,MBC与更差的PFS和OS显著相关。MBC患者对传统CT药物耐药,需要更有效的治疗方案。