Suppr超能文献

乳腺癌患者新辅助化疗病理反应的预测因素

Predictive factors of pathological response to neoadjuvant chemotherapy in patients with breast cancer.

作者信息

Ryspayeva Dinara, Lyashenko Andrey, Dosenko Irina, Kostryba Oleksey, Koshyk Olena, Krotevych Mykhailo, Smolanka Ivan

机构信息

Department of Oncohematology and Adjuvant Treatment Methods, National Cancer Institute, Kyiv, Ukraine.

出版信息

J BUON. 2020 Jan-Feb;25(1):168-175.

Abstract

PURPOSE

To identify predictive factors connected with pathologic response in patients with breast cancer (BC) having received neoadjuvant chemotherapy (NACT).

METHODS

49 patients with BC were investigated before and after treatment in this prospective research. Different chemotherapy regimes were administered. The Miller-Payne scoring system was used to assess the tumour response. The nuclear proliferation markers Ki67 and the expression of topoisomerase IIα (Topo IIα) were evaluated.

RESULTS

Six patients (12.2 %) achieved pathological complete response (pCR). Noticeable decrease of tumor cellularity was detected in all BC subtypes and pCR in the triple-negative BC (TNBC) group (p=0.007) was observed. Poorly differentiated tumors could be considered as predictive factors of pCR (p=0.07). Ki67 appeared to be a predictive marker of achieving pCR (p<0.001) with a threshold of 28% (AUC=0.89, 95% CI 0.75-0.96). The additional factor of reaching pCR was operable BC (p=0.04). The expression level of Topo IIα (p=0.50) and using different regimens of NACT (p=0.97) did not influence pCR achievement.

CONCLUSION

To sum it up, poorly differentiated carcinomas with high cellularity in the primary tumor, TNBC, Ki 67 with a threshold above 28% and operable BC can be considered as early predictors of reaching pCR.

摘要

目的

确定接受新辅助化疗(NACT)的乳腺癌(BC)患者中与病理反应相关的预测因素。

方法

在这项前瞻性研究中,对49例BC患者治疗前后进行了调查。采用了不同的化疗方案。使用米勒-佩恩评分系统评估肿瘤反应。评估了核增殖标志物Ki67和拓扑异构酶IIα(Topo IIα)的表达。

结果

6例患者(12.2%)达到病理完全缓解(pCR)。在所有BC亚型中均检测到肿瘤细胞数量明显减少,且在三阴性乳腺癌(TNBC)组中观察到pCR(p = 0.007)。低分化肿瘤可被视为pCR的预测因素(p = 0.07)。Ki67似乎是实现pCR的预测标志物(p < 0.001),阈值为28%(AUC = 0.89,95% CI 0.75 - 0.96)。达到pCR的另一个因素是可手术的BC(p = 0.04)。Topo IIα的表达水平(p = 0.50)和使用不同的NACT方案(p = 0.97)并不影响pCR的实现。

结论

综上所述,原发性肿瘤中细胞数量多的低分化癌、TNBC、阈值高于28%的Ki 67以及可手术的BC可被视为达到pCR的早期预测因素。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验