机构地区:[1]江西省肿瘤医院乳腺外科,南昌市330029 [2]江西省肿瘤医院病理科,南昌市330029
出 处:《中国肿瘤临床》2009年第3期126-130,共5页Chinese Journal of Clinical Oncology
摘 要:目的:本文分析三阴乳腺癌(缺乏ER、PR、HER-2表达)对含蒽环类方案新辅助化疗的反应、远期疗效和探讨可能的机制。方法:对2000年1月至2003年12月间用含蒽环类方案新辅助化疗的有长期随访资料(中位随访期5.4年)的326例乳腺癌患者进行分析,用免疫组化检测ER、PR、HER-2、p53、Ki67、E钙粘素的表达,采用Cox风险回归模型分析影响无复发生存率(relapse—freesurvival rate,RFS)和总生存率(overallsurvival rate,0S)的预后因素,比较三阴乳腺癌和非三阴乳腺癌对含蒽环类方案新辅助化疗的反应,RFS和OS,分析三阴表型与肿瘤分级、p53、Ki67、E钙粘素表达的关系。结果:三阴表型、肿瘤分期、组织学分级、对新辅助化疗的临床反应及pCR是影响乳腺癌预后的独立因素;三阴乳腺癌占全组病例的21.5%,与非三阴乳腺癌比较,三阴乳腺癌组有较高的pCR率(P=0.046)和临床反应率(P=0.037),但RFS及OS低于非三阴组(P=0.001,P=O.004);新辅助化疗后达到临床缓解的三阴乳腺癌RFS和OS并未得到改善;三阴乳腺癌与p53和Ki67的表达呈正相关(P=0.007,P=0.028),与E钙粘素的表达呈负相关(P=0.034)。结论:三阴乳腺癌对含蒽环类药物方案新辅助化疗的临床反应率和pCR率均较高,但远期疗效却较差。其机制可能与三阴乳腺癌具有较高的增殖、侵袭转移能力和缺乏有效的治疗靶点有关。Objective: Triple-negative breast cancer (TNBC) is defined by the lack of estrogen receptor (ER), progesterone receptor (PR), and human epidermal growth factor receptor 2 (HER-2) expression. This study was to compare response to neoadjuvant chemotherapy with anthracycline-based regimen and prospective efficacy between patients with TNBC and those without TNBC, and to investigate the mechanisms of the effect of TNBC on patient survival. Methods: A total of 326 patients who received neoadjuvant chemotherapy with anthracycline-based regimen between 2000 and 2003 and had complete data about long-term clinical follow-up (5.4 years on average) were reviewed. Expressions of ER, PR, HER-2, P53, Ki67 and E-cadherin were detected by immunohistochemical staining. A multivariate Cox regression analysis was carried out to evaluate independent predictive factors for relapse-free survival rate (RFS) and overall survival rate (OS). Clinical response rate, pathologic complete response (pCR) rate, and expression of P53, Ki67, and E-cadherin were compared between TNBC patients and non-TNBC patients. Results: TNBC, stage, histologic grade, clinical response and pCR were independent prognostic factors associated with survival rates. Seventy (21.5%) of the 326 patients had TNBC. Compared with non-TNBC patients, TNBC patients had significantly higher pCR rate (P=0.046) and clinical response rate (P=0.037) and lower 5-year RFS rate (P=0.001) and 5-year OS (P=0.004). RFS and OS were not improved in TNBC patients after neoadjuvant chemotherapy. Levels of P53 and Ki67 were positively correlated with triple-negative phenotype (P=0.007 and P=0.028, respectively). E-cadherin level was inversely associated with triple-negative phenotype (P=0.034). Conclusion: Neoadjuvant anthracycline-based regimen chemotherapy has poorer efficacy in TNBC patients than in non-TNBC patientsl The poor prognosis of TNBC may be attributed to its growth potential, aggressive biological behavior and
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