Department of Breast Medical Oncology, Division of Cancer Medicine, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Hillman Cancer Center, University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania, USA.
Oncologist. 2020 Feb;25(2):e214-e222. doi: 10.1634/theoncologist.2019-0446. Epub 2019 Oct 14.
BACKGROUND: Limited data exist describing real-world treatment of de novo and recurrent HER2-positive metastatic breast cancer (MBC). MATERIALS AND METHODS: The Systemic Therapies for HER2-Positive Metastatic Breast Cancer Study (SystHERs) was a fully enrolled (2012-2016), observational, prospective registry of patients with HER2-positive MBC. Patients aged ≥18 years and ≤6 months from HER2-positive MBC diagnosis were treated and assessed per their physician's standard practice. The primary endpoint was to characterize treatment patterns by de novo versus recurrent MBC status, compared descriptively. Secondary endpoints included patient characteristics, progression-free and overall survival (PFS and OS, by Kaplan-Meier method; hazard ratio [HR] and 95% confidence interval [CI] by Cox regression), and patient-reported outcomes. RESULTS: Among 977 eligible patients, 49.8% (n = 487) had de novo and 50.2% (n = 490) had recurrent disease. A higher proportion of de novo patients had hormone receptor-negative disease (34.9% vs. 24.9%), bone metastasis (57.1% vs. 45.9%), and/or liver metastasis (41.9% vs. 33.1%), and a lower proportion had central nervous system metastasis (4.3% vs. 13.5%). De novo patients received first-line regimens containing chemotherapy (89.7%), trastuzumab (95.7%), and pertuzumab (77.8%) more commonly than recurrent patients (80.0%, 85.9%, and 68.6%, respectively). De novo patients had longer median PFS (17.7 vs. 11.9 months; HR, 0.69; 95% CI, 0.59-0.80; p < .0001) and OS (not estimable vs. 44.5 months; HR, 0.55; 95% CI, 0.44-0.69; p < .0001). CONCLUSION: Patients with de novo versus recurrent HER2-positive MBC exhibit different disease characteristics and survival durations, suggesting these groups have distinct outcomes. These differences may affect future clinical trial design. Clinical trial identification number. NCT01615068 (clinicaltrials.gov). IMPLICATIONS FOR PRACTICE: SystHERs was an observational registry of patients with HER2-positive metastatic breast cancer (MBC), which is a large, modern, real-world data set for this population and, thereby, provides a unique opportunity to study patients with de novo and recurrent HER2-positive MBC. In SystHERs, patients with de novo disease had different baseline demographics and disease characteristics, had superior clinical outcomes, and more commonly received first-line chemotherapy and/or trastuzumab versus those with recurrent disease. Data from this and other studies suggest that de novo and recurrent MBC have distinct outcomes, which may have implications for disease management strategies and future clinical study design.
背景:目前关于新诊断和复发的人表皮生长因子受体 2 阳性转移性乳腺癌(MBC)的真实世界治疗数据十分有限。
材料与方法:系统治疗 HER2 阳性转移性乳腺癌研究(SystHERs)是一项完全入组(2012-2016 年)、观察性、前瞻性的 HER2 阳性 MBC 患者注册研究。年龄≥18 岁且≤6 个月的 HER2 阳性 MBC 患者按医生的标准治疗进行评估。主要终点是通过描述性比较,按新诊断和复发 MBC 状态描述治疗模式。次要终点包括患者特征、无进展生存期(PFS)和总生存期(OS)[通过 Kaplan-Meier 法评估;风险比(HR)和 95%置信区间(CI)通过 Cox 回归法评估],以及患者报告的结局。
结果:在 977 例符合条件的患者中,49.8%(n=487)为新诊断,50.2%(n=490)为复发。新诊断患者中,激素受体阴性疾病(34.9% vs. 24.9%)、骨转移(57.1% vs. 45.9%)和/或肝转移(41.9% vs. 33.1%)的比例较高,中枢神经系统转移(4.3% vs. 13.5%)的比例较低。新诊断患者更常接受一线含化疗(89.7%)、曲妥珠单抗(95.7%)和帕妥珠单抗(77.8%)的方案,而非复发患者(分别为 80.0%、85.9%和 68.6%)。新诊断患者的中位 PFS(17.7 个月 vs. 11.9 个月;HR,0.69;95%CI,0.59-0.80;p<.0001)和 OS(不可评估 vs. 44.5 个月;HR,0.55;95%CI,0.44-0.69;p<.0001)更长。
结论:新诊断和复发的 HER2 阳性 MBC 患者表现出不同的疾病特征和生存时间,提示这些患者具有不同的结局。这些差异可能会影响未来临床试验的设计。临床试验注册号:NCT01615068(clinicaltrials.gov)。
临床意义:SystHERs 是一项针对 HER2 阳性转移性乳腺癌(MBC)患者的观察性登记研究,这是一项针对该人群的大型、现代、真实世界的数据,因此为研究新诊断和复发的 HER2 阳性 MBC 患者提供了独特的机会。在 SystHERs 中,新发疾病患者的基线特征和疾病特征不同,临床结局更好,且更常接受一线化疗和/或曲妥珠单抗治疗,而非复发患者。来自本研究和其他研究的数据表明,新发和复发的 MBC 具有不同的结局,这可能对疾病管理策略和未来的临床研究设计产生影响。
Breast Cancer Res Treat. 2020-11
Breast Cancer Res Treat. 2014-6
Adv Exp Med Biol. 2025
Med Oncol. 2024-9-25
J Natl Cancer Inst. 2018-6-1
Breast Cancer Res Treat. 2017-10-16
Cancer Epidemiol Biomarkers Prev. 2017-6
N Engl J Med. 2015-2-19
J Natl Cancer Inst. 2014-4-28
Breast Cancer Res Treat. 2014-6