Elnemr Gamal M, El-Rashidy Ahmed H, Osman Ahmed H, Issa Lotfi F, Abbas Osama A, Al-Zahrani Abdullah S, El-Seman Sheriff M, Mohammed Amrallah A, Hassan Abdelghani A
Department of Internal Medicine, Faculty of Medicine, Taif University, Taif, Saudi Arabia E-mail :
Asian Pac J Cancer Prev. 2016;17(2):807-13. doi: 10.7314/apjcp.2016.17.2.807.
Triple-negative breast cancers constitute about 15% of all cases, but despite their higher response to neoadjuvant chemotherapy, the tumors are very aggressive and associated with a poor prognosis as well as a higher risk of early recurrence. This study was retrospectively performed on 101 patients with stage II and III invasive breast cancer who received 6-8 cycles of neo-adjuvant chemotherapy. Out of the total, 23 were in the triple negative breast cancer subgroup. Nuclear Ki-67 expression in both the large cohort group (n=101) and triple negative breast cancer subgroup (n=23) and its relation to the pathological response were evaluated. The purpose of the study was to identify the predictive value of nuclear protein Ki-67 expression among patients with invasive breast cancers, involving the triple negative breast cancer subgroup, treated with neoadjuvant chemotherapy in correlation to the rate of pathological complete response. The proliferation marker Ki-67 expression was highest in the triple negative breast cancer subgroup. No appreciable difference in the rate of Ki-67 expression in triple negative breast cancer subgroup using either a cutoff of 14% or 35%. Triple negative breast cancer subgroup showed lower rates of pathological complete response. Achievement of pathological complete response was significantly correlated with smaller tumor size and higher Ki-67 expression. The majority of triple negative breast cancer cases achieved pathological partial response. The study concluded that Ki-67 is a useful tool to predict chemosensitivity in the setting of neoadjuvant chemotherapy for invasive breast cancer but not for the triple negative breast cancer subgroup.
三阴性乳腺癌约占所有病例的15%,尽管它们对新辅助化疗的反应较高,但这些肿瘤极具侵袭性,预后较差,早期复发风险也更高。本研究对101例接受6 - 8周期新辅助化疗的II期和III期浸润性乳腺癌患者进行了回顾性研究。其中,23例属于三阴性乳腺癌亚组。评估了大样本队列组(n = 101)和三阴性乳腺癌亚组(n = 23)中核Ki-67的表达及其与病理反应的关系。本研究的目的是确定在接受新辅助化疗的浸润性乳腺癌患者(包括三阴性乳腺癌亚组)中,核蛋白Ki-67表达与病理完全缓解率相关的预测价值。增殖标志物Ki-67的表达在三阴性乳腺癌亚组中最高。使用14%或35%的临界值时,三阴性乳腺癌亚组中Ki-67的表达率没有明显差异。三阴性乳腺癌亚组的病理完全缓解率较低。病理完全缓解的实现与较小的肿瘤大小和较高的Ki-67表达显著相关。大多数三阴性乳腺癌病例达到了病理部分缓解。该研究得出结论,Ki-67是预测浸润性乳腺癌新辅助化疗中化疗敏感性的有用工具,但不适用于三阴性乳腺癌亚组。