Division of Hematology/Oncology, Mayo Clinic, Jacksonville, FL 32224, USA.
Cancer. 2013 Aug 1;119(15):2675-82. doi: 10.1002/cncr.28130. Epub 2013 Jun 6.
Increased soluble human epidermal growth factor receptor 2 (sHER2) is an indicator of a poor prognosis in HER2-positive metastatic breast cancer. In this study, the authors evaluated levels of sHER2 during treatment and at the time of disease recurrence in the adjuvant North Central Cancer Treatment Group N9831 clinical trial.
The objectives were to describe sHER2 levels during treatment and at the time of recurrence in patients who were randomized to treatment arms A (standard chemotherapy), B (standard chemotherapy with sequential trastuzumab), and C (standard chemotherapy with concurrent trastuzumab). Baseline samples were available from 2318 patients, serial samples were available from 105 patients, and recurrence samples were available from 124 patients. The cutoff sHER2 value for the assay was 15 ng/mL. Statistical methods included repeated measures linear models, Wilcoxon rank-sum tests, and Cox regression models.
There were differences between groups in terms of age, menopausal status, and hormone receptor status. Within treatment arms A, B, and C, patients who had baseline sHER2 levels ≥15 ng/mL had worse disease-free survival than patients who had baseline sHER2 levels <15 ng/mL (arm A: hazard ratio, 1.81; P = .0014; arm B: hazard ratio, 2.08; P = .0015; arm C: hazard ratio, 1.96; P = .01). Among the 124 patients who experienced disease recurrence, sHER2 levels increased from baseline to the time of recurrence in arms A and B but remained unchanged in arm C. Patients who had recurrence sHER2 levels ≥15 ng/mL had a shorter survival after recurrence with a 3-year overall survival rate of 51% compared with 77% for those who had recurrence sHER2 levels <15 ng/mL (hazard ratio, 2.36; 95% confidence interval, 1.19-4.70; P = .01).
In patients with early stage, HER2-positive breast cancer, a high baseline sHER2 level was identified as a prognostic marker associated with shorter disease-free survival, and a high sHER2 level at recurrence was predictive of shorter survival.
可溶性人表皮生长因子受体 2(sHER2)升高是 HER2 阳性转移性乳腺癌预后不良的指标。在这项研究中,作者评估了辅助性北中央癌症治疗组 N9831 临床试验中接受治疗和疾病复发时 sHER2 的水平。
目的是描述随机分配到 A 治疗组(标准化疗)、B 治疗组(标准化疗序贯曲妥珠单抗)和 C 治疗组(标准化疗联合曲妥珠单抗)的患者在治疗期间和复发时的 sHER2 水平。2318 例患者有基线样本,105 例患者有连续样本,124 例患者有复发样本。检测的 sHER2 截断值为 15ng/mL。统计方法包括重复测量线性模型、Wilcoxon 秩和检验和 Cox 回归模型。
各组之间在年龄、绝经状态和激素受体状态方面存在差异。在 A、B 和 C 治疗组内,基线 sHER2 水平≥15ng/mL 的患者无病生存期比基线 sHER2 水平<15ng/mL 的患者差(A 组:危险比,1.81;P=0.0014;B 组:危险比,2.08;P=0.0015;C 组:危险比,1.96;P=0.01)。在 124 例发生疾病复发的患者中,A 组和 B 组的 sHER2 水平从基线升高到复发时,但 C 组不变。复发时 sHER2 水平≥15ng/mL 的患者复发后的生存率较短,3 年总生存率为 51%,而复发时 sHER2 水平<15ng/mL 的患者为 77%(危险比,2.36;95%置信区间,1.19-4.70;P=0.01)。
在早期 HER2 阳性乳腺癌患者中,高基线 sHER2 水平被确定为与无病生存期较短相关的预后标志物,而复发时 sHER2 水平升高预示着生存率较短。