Vargas-Roig Laura M, Cuello-Carrión F Darío, Fernández-Escobar Nicolás, Daguerre Pedro, Leuzzi Marcela, Ibarra Jorge, Gago Francisco E, Nadin Silvina B, Ciocca Daniel R
Institute of Medicine and Experimental Biology of Cuyo, Regional Center for Scientific and Technological Research, National Research Council of Argentine, Mendoza 5500, Argentina.
Mol Oncol. 2008 Jun;2(1):102-11. doi: 10.1016/j.molonc.2008.01.004. Epub 2008 Jan 13.
We have analyzed the predictive/prognostic value of Bcl-2 protein in breast cancer patients treated with neoadjuvant chemotherapy. One hundred and ten patients were submitted to two different chemotherapeutic regimens: a) 5-fluorouracil, adriamycin or epirubicin, and cyclophosphamide (FAC/FEC) during 2-6 cycles before surgery and 3 or 4 additional cycles of FAC/FEC after surgery (n=40) and b) doxorubicin (D) 75 mg/m(2) or epirubicin (E) 120 mg/m(2) during 4 cycles before surgery, and 6 cycles of cyclophosphamide, methotrexate, and 5-fluorouracil (CMF) after surgery (n=70). Bcl-2 expression, evaluated by immunohistochemistry, did not change significantly after chemotherapy and was not related to clinical/pathological response. In FAC/FEC group, Bcl-2 positive expression after chemotherapy correlated with better disease free survival (DFS) and overall survival (OS) (P=0.008 and P=0.001). In D/E group, Bcl-2 also correlated with better DFS and OS (P=0.03 and P=0.054) in the post-chemotherapy biopsies. An unusual nuclear localization of Bax was observed in some biopsies, but this localization did not correlate with the tumor response or outcome of the patients. We found that a high Bcl-2 expression had no predictive value but had prognostic value in breast cancer patients treated with neoadjuvant anthracycline based chemotherapy.
我们分析了Bcl-2蛋白在接受新辅助化疗的乳腺癌患者中的预测/预后价值。110例患者接受了两种不同的化疗方案:a)术前2 - 6个周期使用5-氟尿嘧啶、阿霉素或表柔比星以及环磷酰胺(FAC/FEC),术后再进行3或4个周期的FAC/FEC(n = 40);b)术前4个周期使用阿霉素(D)75 mg/m²或表柔比星(E)120 mg/m²,术后进行6个周期的环磷酰胺、甲氨蝶呤和5-氟尿嘧啶(CMF)(n = 70)。通过免疫组织化学评估,化疗后Bcl-2表达无显著变化,且与临床/病理反应无关。在FAC/FEC组中,化疗后Bcl-2阳性表达与更好的无病生存期(DFS)和总生存期(OS)相关(P = 0.008和P = 0.001)。在D/E组中,化疗后活检中Bcl-2也与更好的DFS和OS相关(P = 0.03和P = 0.054)。在一些活检中观察到Bax有异常的核定位,但这种定位与患者肿瘤反应或预后无关。我们发现,在接受基于蒽环类药物的新辅助化疗的乳腺癌患者中,高Bcl-2表达无预测价值,但具有预后价值。