Prognostic significance of bcl-2 expression in stage III breast cancer patients who had received doxorubicin and cyclophosphamide followed by paclitaxel as adjuvant chemotherapy.

Prognostic significance of bcl-2 expression in stage III breast cancer patients who had received doxorubicin and cyclophosphamide followed by paclitaxel as adjuvant chemotherapy.
复制标题

DOI:
10.1186/1471-2407-7-63
复制
发表时间:
2007-04-12
期刊:
影响因子:
3.8
通讯作者:
Bang YJ
Bang YJ
中科院分区:
医学2区
文献类型:
--
作者:
Lee KH;Im SA;Oh DY;Lee SH;Chie EK;Han W;Kim DW;Kim TY;Park IA;Noh DY;Heo DS;Ha SW;Bang YJ

文献摘要

参考文献

被引文献

相似文献

Bcl-2在乳腺癌中受到激素受体途径的正调控。进行了一项研究,以评估临床病理变量和ER,PR,p53,c-erbB 2,bcl-2,或Ki-67作为乳腺癌患者复发标志物的预后意义,这些患者在同一个机构接受了相同的辅助治疗。对151例根治性切除的III期乳腺癌患者(男:女= 3:148,中位年龄46岁)进行临床病理特征分析,这些患者有4个或更多阳性淋巴结,接受阿霉素和环磷酰胺,随后接受紫杉醇(AC/T)作为辅助化疗,包括无病生存期(DFS)和总生存期(OS)。ER和/或PR表达阳性的患者在AC/T后接受了5年的他莫昔芬治疗。生物标志物的蛋白质表达进行了化学评价。中位随访时间为36个月,37例患者(24.5%)复发。单因素分析显示肿瘤大小(P = 0.038)和淋巴结转移(P < 0.001)对复发有显著影响。然而,手术类型、组织学、组织学分级、内淋巴管栓塞的存在和近切缘并不影响。ER阳性(P = 0.013)、bcl-2阳性(P = 0.002)和p53低表达(P = 0.032)与DFS延长显著相关。多因素分析显示10个或更多淋巴结受累(HR 7.366; P < 0.001)、bcl-2阴性表达(HR 2.895; P = 0.030)和c-erbB 2过表达(HR 3.535; P = 0.001)是DFS较差的独立指标。bcl-2表达与ER、PR表达呈显著相关,与p53、c-erbB 2、Ki-67表达呈负相关。bcl-2阳性表达者DFS明显长于阴性表达者,即使在ER(+)亚组中也是如此。ER、bcl-2和c-erbB 2对OS有显著影响。Bcl-2是根治性切除的III期乳腺癌患者DFS的独立预后因素,与c-erbB 2和受累淋巴结数量联合似乎是一个有用的预后因素。
Bcl-2 is positively regulated by hormonal receptor pathways in breast cancer. A study was conducted to assess the prognostic significances of clinico-pathologic variables and of ER, PR, p53, c-erbB2, bcl-2, or Ki-67 as markers of relapse in breast cancer patients who had received the identical adjuvant therapy at a single institution. A cohort of 151 curatively resected stage III breast cancer patients (M:F = 3:148, median age 46 years) who had 4 or more positive lymph nodes and received doxorubicin and cyclophosphamide followed by paclitaxel (AC/T) as adjuvant chemotherapy was analyzed for clinico-pathologic characteristics including disease-free survival (DFS) and overall survival (OS). Patients with positive ER and/or PR expression received 5 years of tamoxifen following AC/T. The protein expressions of biomarkers were assessed immunohistochemically. The median follow-up duration was 36 months, and 37 patients (24.5%) experienced a recurrence. Univariate analyses indicated that the tumor size (P = 0.038) and the number of involved lymph nodes (P < 0.001) significantly affected the recurrences. However, the type of surgery, the histology, histologic grade, the presence of endolymphatic emboli, and a close resection margin did not. Moreover, ER positivity (P = 0.013), bcl-2 positivity (P = 0.002) and low p53 expression (P = 0.032) were found to be significantly associated with a prolonged DFS. Furthermore, multivariate analysis identified 10 or more involved lymph nodes (HR 7.366; P < 0.001), negative bcl-2 expression (HR 2.895; P = 0.030), and c-erbB2 over-expression (HR 3.535; P = 0.001) as independent indicators of poorer DFS. In addition, bcl-2 expression was found to be significantly correlated with the expressions of ER and PR, and inversely correlated with the expressions of p53, c-erbB2 and Ki-67. Patients with bcl-2 expression had a significantly longer DFS than those without, even in the ER (+) subgroup. Moreover, OS was significantly affected by ER, bcl-2 and c-erbB2. Bcl-2 is an independent prognostic factor of DFS in curatively resected stage III breast cancer patients and appears to be a useful prognostic factor in combination with c-erbB2 and the number of involved lymph nodes.
DOI: 10.1056/nejmoa043681
发表时间: 2005-06-02
影响因子: 158.5
作者:
Martin, M;Pienkowski, T;Vogel, C
通讯作者: Vogel, C
DOI: 10.1038/bjc.1996.319
发表时间: 1996-07-01
影响因子: 8.8
作者:
vanSlooten, HJ;Clahsen, PC;vandeVijver, MJ
通讯作者: vandeVijver, MJ
DOI: 10.1200/jco.2003.02.063
发表时间: 2003-03-15
影响因子: 45.3
作者:
Henderson, IC;Berry, DA;Norton, L
通讯作者: Norton, L
DOI: 10.1124/mol.64.1.51
发表时间: 2003-07-01
影响因子: 3.6
作者:
Ferlini, C;Raspaglio, G;Scambia, G
通讯作者: Scambia, G
DOI: 10.1056/nejmoa021967
发表时间: 2002-12-19
影响因子: 158.5
作者:
van de Vijver, MJ;He, YD;Bernards, R
通讯作者: Bernards, R