Prognostic value of receptor status conversion following neoadjuvant chemotherapy in breast cancer patients: a systematic review and meta-analysis

被引:0
作者
Chao Li
Hongwei Fan
Qian Xiang
Ling Xu
Zhuo Zhang
Qianxin Liu
Tongtong Zhang
Jinjie Ling
Ying Zhou
Xia Zhao
Yimin Cui
机构
[1] Peking University First Hospital,Department of Pharmacy
[2] Chinese Academy of Medical Sciences and Peking Union Medical College,National Cancer Center/Cancer Hospital & Shenzhen Hospital
[3] Peking University First Hospital,Breast Disease Center
[4] Duke University,Department of Biology
来源
Breast Cancer Research and Treatment | 2019年 / 178卷
关键词
Breast cancer; Neoadjuvant chemotherapy; Receptor; Prognosis;
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学科分类号
摘要
Biomarkers of breast cancer such as hormone receptors (HR) and human epidermal growth factor 2 (HER2) can be altered after neoadjuvant chemotherapy (NAC). However, whether the conversion of these receptors affects the prognosis of patients remains to be determined. We sought to evaluate the prognostic value of HR and HER2 receptors before and after NAC and to analyze their clinical implications. Relevant studies were used to calculate the pooled hazard ratios, 95% confidence interval (95% CI). This meta-analysis included eight studies with 2847 patients. Compared to patients with HR+ → +, patients with HR+ → − have shorter disease free survival (DFS) (hazard ratio = 2.64, 95% CI 1.86–3.75) and overall survival (OS) (hazard ratio = 2.99, 95% CI 1.97–4.54). Furthermore, patients with HR− → + tend to achieve better DFS (hazard ratio = 0.83, 95% CI 0.60–1.17) compared to patients with HR− → −. Patients with HR− → + gain better OS (hazard ratio = 0.67, 95% CI 0.46–0.99) compared to patients exhibiting HR− → −. When comparing patients with HER2+ → − to patients with HER2+ → +, patients with HER2+ → − tended to achieve better DFS (hazard ratio = 1.65, 95% CI 1.08–2.53) though results for OS (hazard ratio = 1.16, 95% CI 0.54–2.49) were not statistically significant. Our data strongly support the need for redetection of HR and HER2 receptor status of surgical sample following neoadjuvant therapy. Changes in HR status induced by NAC can be used as a prognostic factor in breast cancer patients for predicting both OS and DFS. HER2 change may also be valuable for predicting prognosis. Further research should explore therapeutic strategies for those presenting receptor status conversion.
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页码:497 / 504
页数:7
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共 90 条
[1]  
Fisher B(1998)Effect of preoperative chemotherapy on the outcome of women with operable breast cancer J Clin Oncol Off J Am Soc Clin Oncol 16 2672-2685
[2]  
Bryant J(2005)Neoadjuvant versus adjuvant systemic treatment in breast cancer: a meta-analysis Breast Dis A Year Book Q 97 188-194
[3]  
Wolmark N(2012)Definition and impact of pathologic complete response on prognosis after neoadjuvant chemotherapy in various intrinsic breast cancer subtypes J Clin Oncol Off J Am Soc Clin Oncol 30 1796-1804
[4]  
Mauri D(2011)Meta-analysis confirms achieving pathological complete response after neoadjuvant chemotherapy predicts favourable prognosis for breast cancer patients Eur J Cancer 47 2084-2090
[5]  
Pavlidis N(2012)Meta-analysis of the association of breast cancer subtype and pathologic complete response to neoadjuvant chemotherapy Eur J Cancer 48 3342-3354
[6]  
Ioannidis JPA(1991)Hormonal receptors in locally advanced breast cancer: change with response to neoadjuvant chemotherapy? J Surg Oncol 46 156-158
[7]  
Von MG(2009)Change in the hormone receptor status following administration of neoadjuvant chemotherapy and its impact on the long-term outcome in patients with primary breast cancer Br J Cancer 101 1529-1536
[8]  
Untch M(2008)Changes in tumour biological markers during primary systemic chemotherapy (PST) Anticancer Res 28 1797-430
[9]  
Blohmer JU(2011)Discordances in ER, PR and HER2 receptors after neoadjuvant chemotherapy in breast cancer Cancer Treat Rev 37 422-599
[10]  
Kong X(2011)The hormonal receptor status in breast cancer can be altered by neoadjuvant chemotherapy: a meta-analysis Cancer Invest 29 594-9611