曲妥珠单抗
曲妥珠单抗
乳腺癌
医学
肿瘤科
内科学
残余物
癌症
计算机科学
算法
作者
Charles E. Geyer,M. Untch,Chiun‐Sheng Huang,Max S. Mano,Eleftherios P. Mamounas,Norman Wolmark,Priya Rastogi,Andreas Schneeweiß,Andrés Redondo,Hans Holger Fischer,Véronique D’Hondt,Alison Conlin,Valentina Guarneri,Irene Wapnir,Christian Jackisch,Claudia Arce-Salinas,Peter A. Fasching,Michael P. DiGiovanna,John Crown,Pia Wuelfing
标识
DOI:10.1056/nejmoa2406070
摘要
BackgroundPatients with human epidermal growth factor receptor 2 (HER2)–positive early breast cancer with residual invasive disease after neoadjuvant systemic therapy have a high risk of recurrence and death. The primary analysis of KATHERINE, a phase 3, open-label trial, showed that the risk of invasive breast cancer or death was 50% lower with adjuvant trastuzumab emtansine (T-DM1) than with trastuzumab alone.MethodsWe randomly assigned patients with HER2-positive early breast cancer with residual invasive disease in the breast or axilla after neoadjuvant systemic treatment with taxane-based chemotherapy and trastuzumab to receive T-DM1 or trastuzumab for 14 cycles. Here, we report the prespecified final analysis of invasive disease–free survival and the second interim analysis of overall survival.Download a PDF of the Plain Language Summary.ResultsWith a median follow-up of 8.4 years, T-DM1 sustained the improvement in invasive disease–free survival over trastuzumab (unstratified hazard ratio for invasive disease or death, 0.54; 95% confidence interval [CI], 0.44 to 0.66). Seven-year invasive disease–free survival was 80.8% with T-DM1 and 67.1% with trastuzumab (difference, 13.7 percentage points). T-DM1 also led to a significantly lower risk of death than trastuzumab (unstratified hazard ratio, 0.66; 95% CI, 0.51 to 0.87; P=0.003). Seven-year overall survival was 89.1% with T-DM1 and 84.4% with trastuzumab (difference, 4.7 percentage points). Adverse events of grade 3 or higher were noted in 26.1% of the patients in the T-DM1 group and 15.7% of those in the trastuzumab group.ConclusionsAs compared with trastuzumab, T-DM1 improved overall survival with sustained improvement in invasive disease–free survival among patients with HER2-positive early breast cancer with residual invasive disease after neoadjuvant therapy. (Funded by F. Hoffmann–La Roche/Genentech; KATHERINE ClinicalTrials.gov number, NCT01772472.) Quick Take Trastuzumab Emtansine in Residual HER2-Positive Breast Cancer 2m 35s
科研通智能强力驱动
Strongly Powered by AbleSci AI