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TOPOⅡ和P53与乳腺癌新辅助化疗疗效的关系研究 被引量:1

Levels of TOPO Ⅱ and P53 predict the efficacy of neoadjuvant chemotherapy in breast cancer
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摘要 目的本研究旨在检测化疗前乳腺癌组织中TOPOⅡ和P53的表达情况,探讨二者与新辅助化疗疗效之间的关系。方法本研究回顾性分析了我院乳腺肿瘤医学部自2011年10月至2015年8月接受以蒽环类为基础新辅助化疗的Ⅱ~Ⅲ期浸润性导管癌患者185例,化疗前用空心针穿刺活检,按常规免疫组化的方法检测TOPOⅡ、P53的表达情况。统计学分析TOPOⅡ、P53的表达水平与患者临床病理特征及与新辅助化疗效果的关系。结果TOPOⅡ阳性的患者中达到客观缓解的较表达阴性比例更大(P=0.002),P53阳性的患者中达到临床完全缓解的比例比阴性患者更大(P=0.015),TOPOII及P53均为阳性的患者达到临床完全缓解及客观缓解的比例均较高(P=0.010及P=0.027)。结论新辅助化疗前乳腺癌组织中TOPOⅡ和P53的表达水平对新辅助化疗有良好的预测效果。 Objective To investigate whether the expression of TOPO Ⅱ and P53 expression in breast cancer could predict the efficacy of neoadjuvant chemotherapy. Methods This research retrospectively analyzed 185 patients, who were diagnosed as invasive ductal carcinomas in stage Ⅱ-Ⅲ, admitted in the Breast Cancer Center in our hospital and accepted NAC from October 2011 to August 2015. Immunohistochemical assay was used to detect the TOPO Ⅱ and P53 protein levels of185 breast cancer tissues obtained by core needle biopsy before neoadjuvant chemotherapy. The relationship of TOPO Ⅱ and P53 expression with clinicopathological characteristics as well as prognosis of neoadjuvant chemotherapy was statistically analyzed. Results The objective response rate(ORR)of patients with positive TOPO Ⅱ expression was significantly higher than that of patients with negative TOPO Ⅱ expression. The clinical complete response(c CR) proportion of patients with positive P53 expression was larger than that of patients with negative P53 expression. The patients with both positive TOPO Ⅱ and P53 expression not only achieved a higher rate of ORR but had a larger proportion of c CR than the case in patients not with both positive TOPO Ⅱ and P53 expression.Conclusion The protein levels of TOPO Ⅱ and P53 showed predictive value of the efficacy of neoadjuvant chemotherapy based on anthracyclines.
出处 《岭南现代临床外科》 2016年第2期127-131,共5页 Lingnan Modern Clinics in Surgery
基金 国家自然科学基金(81272893) 国家自然科学基金(81472466) 教育部新世纪优秀人才(NCET-12-0565) 广东省杰出青年科学基金(2014A03036003) 中山大学孙逸仙纪念医院优秀青年科学基金(Y201401)
关键词 乳腺癌 拓扑异构酶Ⅱ P53 新辅助化疗 Breast cancer TOPOⅡ P53 Neoadjuvant chemotherapy
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  • 1Kravchenko J, Akushevich I, Seewaldt VL, et al. Breast heterogeneous disease : contributing factors and carcinogenesis mechanisms [J]. Breast Cancer Res Treat, 2011, 128(2): 483-493.
  • 2Van Minckwitz, G Untch M, Blohmer JU, et al. Definition and impact of pathologic complete response on prognosis after neoadjuvant chemotherapy in various intrinsic breast cancer subtypes[J]. J Clin Oneol, 2012, 30(15): 1796-1804.
  • 3Berger JM, Gamblin SJ, Harrison SC, et al. Strueture and mechanism of DNA topoisomerase II [J]. Nature, 1996, 379 (6562) : 225-232.
  • 4Muller PA, Vousden KH. p53 mutations in cancer [J]. Nat Cell Biol, 2013, 15(1): 2-8.
  • 5Reinholz MM, Bruzek AK, Visscher DW, et al. Breast cancer and ancusomy 17: implications for carcinogenesis and therapeutic response[J]. Lancet Oneol, 2009, 10(3): 267- 277.
  • 6Chen S, Huang L, Liu Y, et al. The predictive and prognostic significance of pre- and post-treatment topoisomerase Ilalpha in anthraeyeline-based neoadjuvant chemotherapy for local advanced breast cancer [J]. Eur J Surg Oncol, 2013, 39 (6) : 619-626.
  • 7Kobayashi T, Iwaya K, Moriya T, ct al. A simple immunohist- ochemieal panel comprising 2 conventional markers, Ki67 and p53,is a powerful tool for predicting patient outcome in luminal-type breast cancer[J]. BMC Clin Pathol, 2013, 13: 5.
  • 8Millar EK, Graham PH, McNeil CM, et al. Predietion of outcome of early ER + breast cancer is improved using a biomarker panel, which includes Ki-67 and p53 [J]. Br JCancer, 2011, 105(2): 272-280.
  • 9Nguyen SM, Thamm DH, Vail DM, et al. Response evaluation criteria for solid tumours in dogs (vl.0):a Veterinary Cooperative Oncology Group (VCOG) consensus document [J]. Vet Comp Oncol, 2015, 13(3): 176-183.
  • 10Fumagalli D, Bedard PL, Nahleh Z, et al. A common language in neoadjuvant breast cancer clinical trials: proposals for standard definitions and endpoints[J]. Lancet Oncol, 2012, 13(6) : e240-248.

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