Ryspayeva Dinara, Lyashenko Andrey, Dosenko Irina, Kostryba Oleksey, Koshyk Olena, Krotevych Mykhailo, Smolanka Ivan
Department of Oncohematology and Adjuvant Treatment Methods, National Cancer Institute, Kyiv, Ukraine.
J BUON. 2020 Jan-Feb;25(1):168-175.
To identify predictive factors connected with pathologic response in patients with breast cancer (BC) having received neoadjuvant chemotherapy (NACT).
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.
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.
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.
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。
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。
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。
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。