Tripsianis Gregory, Papadopoulou Evropi, Romanidis Konstantinos, Katotomichelakis Michael, Anagnostopoulos Kostas, Kontomanolis Emmanuel, Botaitis Sotirios, Tentes Ioannis, Kortsaris Alexandros
Laboratory of Medical Statistics, Medical School, Democritus University of Thrace, Alexandroupolis, Greece E-mail :
Asian Pac J Cancer Prev. 2013;14(11):6813-20. doi: 10.7314/apjcp.2013.14.11.6813.
The present study was conducted to investigate the prognostic significance of co-expression patterna of HER-2, IL-6, TNF-a and TGF-β1 in breast cancer, by correlating the number of markers with positive expression with clinicopathological characteristics indicative of tumor progression and overall survival. One hundred thirty consecutive patients with primary breast cancer were prospectively included and evaluated. Serum concentrations of the above markers were measured by ELISA. Median split was used to subdivide patients with marker positive or negative expression. The presence of ≥ 3 positive markers was independently associated with extended lymph node (>3) involvement (aOR, 11.94, p=0.001) and lymphovascular invasion (aOR, 12.04, p=0.018), increasing the prognostic significance of each marker considered separately. Additional prognostic information regarding survival was also provided; as the number of positive markers increased, a gradually reduction of survival time was observed. In addition, patients with 4 positive markers had significantly shorter survival (25 vs 39 months, p=0.006) and a more than 4 fold increased risk of death (aHR, 4.35, p=0.003) compared to patients with 3 positive markers. Our findings suggest that the coexpression pattern of these four markers could be used clinically as a useful marker for tumor extension and outcome of breast cancer.
本研究旨在通过将阳性表达的标志物数量与指示肿瘤进展和总生存的临床病理特征相关联,探讨HER-2、IL-6、TNF-α和TGF-β1共表达模式在乳腺癌中的预后意义。前瞻性纳入并评估了130例连续的原发性乳腺癌患者。通过酶联免疫吸附测定法(ELISA)测量上述标志物的血清浓度。采用中位数分割法将标志物表达阳性或阴性的患者进行细分。≥3个阳性标志物的存在与广泛的淋巴结(>3个)受累(校正比值比[aOR],11.94,p=0.001)和淋巴管浸润(aOR,12.04,p=0.018)独立相关,增加了单独考虑的每个标志物的预后意义。还提供了关于生存的额外预后信息;随着阳性标志物数量的增加,观察到生存时间逐渐缩短。此外,与有3个阳性标志物的患者相比,有4个阳性标志物的患者生存时间显著缩短(25个月对39个月,p=0.006),死亡风险增加超过4倍(校正风险比[aHR],4.35,p=0.003)。我们的研究结果表明,这四种标志物的共表达模式可在临床上用作乳腺癌肿瘤扩展和预后的有用标志物。