预测乳腺癌病理反应和对无病生存的影响的临床病理因素:来自印度南部三级癌症中心的分析

Vishnu Asokan, MeghaP Paramban, M. Tintu, T. Ajayakumar
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摘要

目的:乳腺癌的新辅助化疗导致肿瘤分期降低,并提供了根据反应调整治疗的机会。病理完全缓解(pCR)被认为是预测良好的长期预后。目的是确定与乳腺癌和无病生存(DFS)的pCR相关的临床病理因素。对象与方法:回顾性分析106例接受新辅助治疗的乳腺癌患者的临床病理资料。统计学分析采用SPSS软件(18.0版)的卡方检验。当p值<0.05时认为有统计学意义。结果:患者中位年龄53岁。总pCR率为23.6%。单因素分析显示,Ki-67评分高或分级高的肿瘤中pCR的检出率显著(P = 0.001, P = 0.019)。复发29例,远处转移21例。Kaplan-Meier方法分析显示,与DFS降低相关的统计学显著因素是高Ki 67和淋巴血管侵袭阳性。有pCR的4例发生远处转移,无pCR的19例发生远处转移。pCR和非pCR患者的5年DFS率分别为84%和69%。结论:高分级或Ki-67的肿瘤采用新辅助治疗可获得较高的pCR率。通过获得理想的新辅助选择的pCR,可以获得更长的DFS。
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Clinicopathological factors predictive of pathological response and impact on disease-free survival in breast cancer: Analysis from a tertiary cancer centre in South India
Aim: Neoadjuvant chemotherapy in carcinoma breast results in tumour downstaging and provides the opportunity to modify treatment based on response. Pathological complete response (pCR) is considered predictive of favourable long-term outcomes. The objective was to identify clinicopathological factors associated with pCR in breast cancer and disease-free survival (DFS). Subjects and Methods: Clinicopathological details of 106 breast cancer patients receiving neoadjuvant therapy were retrospectively analyzed. The statistical analyses were performed using the Chi-square test by SPSS software (version 18.0). Pvalues were considered statistically significant when <0.05. Results: The median age of the patients was 53 years. The overall pCR rate was 23.6%. From univariate analysis, a significant rate of pCR was detected in tumours with high grade or high Ki-67 scores (P = 0.001, P = 0.019), respectively. 29 patients relapsed of which 21 were distant metastasis. On Kaplan–Meier method analysis, statistically significant factors associated with decreased DFS were high Ki 67 and lymphovascular invasion positivity. Distant metastasis occurred in 4 patients with pCR and 19 patients without pCR. The 5-year DFS rate was 84% versus 69% in patients with pCR and without pCR, respectively. Conclusion: A higher rate of pCR was obtained with neoadjuvant therapy in tumours with high grade or Ki-67. Longer DFS is achieved by obtaining pCR with ideal neoadjuvant selection.
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