Department of Cancer Biology, Mayo Clinic, Jacksonville, FL, 32224, USA.
Department of Pathology, Medicine and Dermatology, Columbia University Medical Center, New York, NY, 10032, USA.
Breast Cancer Res. 2018 Jun 14;20(1):52. doi: 10.1186/s13058-018-0989-8.
Resected HER2 breast cancer patients treated with adjuvant trastuzumab and chemotherapy have superior survival compared to patients treated with chemotherapy alone. We previously showed that trastuzumab and chemotherapy induce HER2-specific antibodies which correlate with improved survival in HER2 metastatic breast cancer patients. It remains unclear whether the generation of immunity required trastuzumab and whether endogenous antibody immunity is associated with improved disease-free survival in the adjuvant setting. In this study, we addressed this question by analyzing serum anti-HER2 antibodies from a subset of patients enrolled in the NCCTG trial N9831, which includes an arm (Arm A) in which trastuzumab was not used. Arms B and C received trastuzumab sequentially or concurrently to chemotherapy, respectively.
Pre-and post-treatment initiation sera were obtained from 50 women enrolled in N9831. Lambda IgG antibodies (to avoid detection of trastuzumab) to HER2 were measured and compared between arms and with disease-free survival.
Prior to therapy, across all three arms, N9831 patients had similar mean anti-HER2 IgG levels. Following treatment, the mean levels of antibodies increased in the trastuzumab arms but not the chemotherapy-only arm. The proportion of patients who demonstrated antibodies increased by 4% in Arm A and by 43% in the Arms B and C combined (p = 0.003). Cox modeling demonstrated that larger increases in antibodies were associated with improved disease-free survival in all patients (HR = 0.23; p = 0.04).
These results show that the increased endogenous antibody immunity observed in adjuvant patients treated with combination trastuzumab and chemotherapy is clinically significant, in view of its correlation with improved disease-free survival. The findings may have important implications for predicting treatment outcomes in patients treated with trastuzumab in the adjuvant setting.
ClinicalTrials.gov, NCT00005970 . Registered on July 5, 2000.
接受曲妥珠单抗和化疗辅助治疗的可切除 HER2 乳腺癌患者的生存优于单独接受化疗的患者。我们之前表明,曲妥珠单抗和化疗诱导了与 HER2 转移性乳腺癌患者生存改善相关的 HER2 特异性抗体。目前尚不清楚是否需要曲妥珠单抗产生免疫,以及内源性抗体免疫是否与辅助治疗中的无病生存改善相关。在这项研究中,我们通过分析 NCCTG 试验 N9831 中入组的一部分患者的血清抗 HER2 抗体来解决这个问题,该试验包括一个未使用曲妥珠单抗的臂(臂 A)。臂 B 和 C 分别顺序或同时接受曲妥珠单抗联合化疗。
从 N9831 入组的 50 名女性中获得治疗前和治疗开始时的血清。测量并比较了三个臂之间以及与无病生存的抗 HER2 免疫球蛋白 G (IgG)抗体和疾病无进展生存。
在所有三个臂中,N9831 患者在治疗前具有相似的平均抗 HER2 IgG 水平。治疗后,曲妥珠单抗组的抗体平均水平升高,但化疗组无升高。抗体增加 4%的患者比例在臂 A 中增加,在臂 B 和 C 联合组中增加 43%(p=0.003)。Cox 模型显示,所有患者中抗体增加越大与无病生存改善相关(HR=0.23;p=0.04)。
这些结果表明,在接受曲妥珠单抗联合化疗辅助治疗的患者中观察到的内源性抗体免疫增加是具有临床意义的,因为它与无病生存改善相关。这些发现可能对预测接受曲妥珠单抗辅助治疗的患者的治疗结果具有重要意义。
ClinicalTrials.gov,NCT00005970。于 2000 年 7 月 5 日注册。