Chinese Journal of Practical Surgery ›› 2024, Vol. 44 ›› Issue (11): 1259-1262.DOI: 10.19538/j.cjps.issn1005-2208.2024.11.14
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周思成1,辛 灵1,江泽飞2,刘荫华1,中国临床肿瘤学会乳腺癌专业委员会,中华医学会外科学分会乳腺外科学组
Abstract: To investigate the status of adjuvant therapy in patients with early-stage human epidermal growth factor receptor 2 (HER2) positive breast cancer in China after dual HER2-targeted neoadjuvant therapy, trastuzumab plus pertuzumab, combined with cytotoxic drugs. Methods The cases of stage Ⅰ-Ⅲ breast cancer treated at 104 hospitals in China between January 1, 2023 and December 31, 2023 were inquired by a questionnaire survey. The investigation included the number of cases, the proportion of HER2-positive breast cancer, the number of cases of HER2-positive breast cancer receiving dual HER2-targeted neoadjuvant therapy, the evaluation method and results of pathological response after neoadjuvant therapy, and adjuvant therapeutic regimen after neoadjuvant therapy. Results A total of 104 hospitals participated in the questionnaire and provided clinicopathological data of 75 530 patients with early-stage breast cancer, and 7063 patients (40.4%) with HER2-positive breast cancer received neoadjuvant therapy with a dual HER2-targeted regimen. 4217 patients (59.7%) achieved pathologic complete response (pCR). The other 2846 patients did not achieved pCR (non-pCR). After dual HER2-targeted neoadjuvant therapy, 5658 patients (80.1%) continued dual HER2-targeted adjuvant therapy, 360 patients (5.1%) received trastuzumab adjuvant therapy, and 1045 patients (14.8%) received other drugs. There was significant difference between adjuvant targeted therapy in different ypTNM group (χ2=1730.058, P<0.001). Conclusion ypTNM stage can provide a basis for formulating follow-up adjuvant therapy regimen for HER2-positive breast cancer patients with non-pCR after dual HER2-targeted neoadjuvant therapy.
Key words: breast cancer, human epidermal growth factor receptor 2 positive, neoadjuvant therapy, dual-targeted therapy, adjuvant therapy
摘要: 目的 调查中国早期HER2阳性乳腺癌病人接受曲妥珠单抗+帕妥珠单抗联合细胞毒药物(简称“双靶”)方案新辅助治疗后辅助治疗现状。方法 采用问卷调查方式登记了2023-01-01—2023-12-31中国104家医院经治的Ⅰ~Ⅲ期乳腺癌病例,调查内容包括收治例数、HER2阳性乳腺癌占比、HER2阳性乳腺癌接受双靶方案新辅助治疗例数、新辅助治疗病理疗效评价方法及结果、双靶新辅助治疗后辅助治疗方案选择情况。结果 全国104家医院提供了75 530例早期乳腺癌病人的临床病理资料。其中,7063例HER2阳性乳腺癌病人接受双靶方案新辅助治疗,4217例(59.7%)病人获得病理完全缓解(pCR),2846例未获得pCR(non-pCR)。双靶新辅助治疗后,5658例(80.1%)沿用双靶辅助治疗,360例(5.1%)仅接受曲妥珠单抗辅助治疗,1045例(14.8%)病人接受其他药物。辅助靶向治疗方案选择与ypTNM分期间差异有统计学意义(χ2=1730.058,P<0.001)。结论 ypTNM分期可能是HER2阳性乳腺癌双靶新辅助治疗后non-pCR病人制定后续辅助治疗方案的依据。
关键词: 乳腺癌, 人类表皮生长因子受体2阳性, 新辅助治疗, 双靶治疗, 辅助治疗
周思成, 辛 灵, 江泽飞, 刘荫华, 中国临床肿瘤学会乳腺癌专业委员会, 中华医学会外科学分会乳腺外科学组. 中国104家医院早期HER2阳性乳腺癌双靶新辅助治疗后辅助治疗现状调查报告(CSBrS-030)[J]. 中国实用外科杂志, 2024, 44(11): 1259-1262.
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https://www.zgsyz.com/zgsywk/EN/Y2024/V44/I11/1259