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Delay in initiation of adjuvant trastuzumab therapy leads to decreased overall survival and relapse-free survival in patients with HER2-positive non-metastatic breast cancer

机译:HER2阳性非转移性乳腺癌患者延迟开始辅助曲妥珠单抗治疗会导致总体生存率降低和无复发生存率

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摘要

Trastuzumab reduces the risk of relapse in women with HER2-positive non-metastatic breast cancer, but little information exists on the timing of trastuzumab initiation. The study investigated the impact of delaying the initiation of adjuvant trastuzumab therapy for >6 months after the breast cancer diagnosis on time to relapse, overall survival (OS), and relapse-free survival (RFS) among patients with non-metastatic breast cancer. Adult women with non-metastatic breast cancer who initiated trastuzumab adjuvant therapy without receiving any neoadjuvant therapy were selected from the US Department of Defense health claims database from 01/2003 to 12/2012. Two study cohorts were defined based on the time from breast cancer diagnosis to trastuzumab initiation: >6 months and ≤6 months. The impact of delaying trastuzumab initiation on time to relapse, OS, and RFS was estimated using Cox regression models adjusted for potential confounders. Of 2749 women in the study sample, 79.9 % initiated adjuvant trastuzumab within ≤6 months of diagnosis and 20.1 % initiated adjuvant trastuzumab >6 months after diagnosis. After adjusting for confounders, patients who initiated trastuzumab >6 months after the breast cancer diagnosis had a higher risk of relapse, death, or relapse/death than those who initiated trastuzumab within ≤6 months of diagnosis (hazard ratios [95 % CIs]: 1.51 [1.22–1.87], 1.54 [1.12–2.12], and 1.43 [1.16–1.75]; respectively). The results of this population-based study suggest that delays of >6 months in the initiation of trastuzumab among HER2-positive non-metastatic breast cancer patients are associated with a higher risk of relapse and shorter OS and RFS.Electronic supplementary materialThe online version of this article (doi:10.1007/s10549-016-3790-3) contains supplementary material, which is available to authorized users.
机译:曲妥珠单抗可降低HER2阳性非转移性乳腺癌女性复发的风险,但关于曲妥珠单抗起始时间的信息很少。这项研究调查了乳腺癌诊断后将曲妥珠单抗辅助治疗的开始推迟超过6个月对非转移性乳腺癌患者的复发时间,总生存期(OS)和无复发生存期(RFS)的影响。从01/2003年至12/2012年从美国国防部健康声明数据库中选择未接受任何新辅助疗法就开始曲妥珠单抗辅助疗法的非转移性乳腺癌成年女性。根据从乳腺癌诊断到曲妥珠单抗开始的时间定义了两个研究队列:> 6个月且≤6个月。使用针对潜在混杂因素调整的Cox回归模型评估了曲妥珠单抗延迟启动对复发时间,OS和RFS的影响。在研究样本中的2749名女性中,诊断后≤6个月内开始使用曲妥珠单抗的辅助率为79.9%,诊断后6个月内开始使用曲妥珠单抗的辅助率为20.1%。调整混杂因素后,在乳腺癌诊断后开始> 6个月开始曲妥珠单抗的患者比在诊断后≤6个月内开始曲妥珠单抗的患者复发,死亡或复发/死亡的风险更高(危险比[95%CIs]:分别为1.51 [1.22-1.87],1.54 [1.12-2.12]和1.43 [1.16-1.75])。这项基于人群的研究结果表明,HER2阳性,非转移性乳腺癌患者中曲妥珠单抗启动延迟超过6个月与复发风险更高,OS和RFS缩短有关。本文(doi:10.1007 / s10549-016-3790-3)包含补充材料,授权用户可以使用。

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