AstraZeneca Pharmaceuticals, Gaithersburg, MD, USA.
Syapse Holdings, Inc., 1442 Pottstown Pike, Unit #3008, West Chester, PA, 19380, USA.
Int J Clin Oncol. 2024 Jun;29(6):780-789. doi: 10.1007/s10147-024-02492-5. Epub 2024 Mar 25.
Standard-of-care for HER2-positive metastatic breast cancer (HER2 + mBC) patients consists of trastuzumab ± pertuzumab with chemotherapy in first-line (1L), and ado-trastuzumab emtansine (T-DM1) or the more recently approved trastuzumab deruxtecan (T-DXd) in second-line (2L). Contemporary data on treatment sequencing and real-world effectiveness is limited. This study aims to report 2L treatments and outcomes among HER2 + mBC patients in the United States (US).
HER2 + mBC patients initiating 2L treatment (index date) between January 2014 and February 2021 were identified from the Syapse Learning Health Network (LHN) database. Summary statistics for patient characteristics, treatment received, reasons for 2L discontinuation and time to 2L-clinical outcomes are reported.
Of the 312 patients initiating 2L treatment, had a median age of 59 years (interquartile range [IQR], 50-66) at the start of 2L. The majority were white (69%) and had de novo mBC (62%). Top three 2L regimens included T-DM1 ± endocrine therapy (29%), trastuzumab/pertuzumab/taxane (10%) and T-DM1/trastuzumab (8%). Around 88% discontinued 2L and 63% received subsequent treatment. Median time-to-next-treatment was 10.6 months (95% CI, 8.8-13.3) and real-world progression-free-survival was 7.9 months (95% CI, 7.0-9.9). Among 274 patients who discontinued 2L, 47% discontinued due to progression and 17% because of intolerance/toxicity, respectively.
This real-world US study showed that approximately two-thirds of 2L patients received subsequent therapy and disease progression was the most common reason for 2L discontinuation highlighting the need for timely 2L treatment with the most efficacious drug to allow patients to achieve longer treatment duration and delayed progression.
曲妥珠单抗联合化疗(1 线)是人表皮生长因子受体 2(HER2)阳性转移性乳腺癌(HER2+MBC)患者的标准治疗方法,而在二线(2 线)治疗中,可使用 ado-曲妥珠单抗emtansine(T-DM1)或最近获批的曲妥珠单抗deruxtecan(T-DXd)。目前关于治疗顺序和真实世界疗效的数据有限。本研究旨在报告美国(US)HER2+MBC 患者的 2 线治疗和结局。
从 Syapse 学习健康网络(LHN)数据库中确定了 2014 年 1 月至 2021 年 2 月期间开始 2 线治疗(索引日期)的 HER2+MBC 患者。报告患者特征、接受的治疗、2 线治疗终止的原因以及 2 线临床结局的时间的汇总统计数据。
在开始 2 线治疗的 312 名患者中,中位年龄为 59 岁(四分位距[IQR],50-66)。大多数为白人(69%),且患有初发 MBC(62%)。排名前三的 2 线方案包括 T-DM1±内分泌治疗(29%)、曲妥珠单抗/帕妥珠单抗/紫杉烷(10%)和 T-DM1/曲妥珠单抗(8%)。约 88%的患者停止了 2 线治疗,63%的患者接受了后续治疗。中位至下一次治疗的时间为 10.6 个月(95%CI,8.8-13.3),真实世界无进展生存期为 7.9 个月(95%CI,7.0-9.9)。在 274 名停止 2 线治疗的患者中,47%因疾病进展而停止治疗,17%因不耐受/毒性而停止治疗。
这项来自美国的真实世界研究表明,约三分之二的 2 线患者接受了后续治疗,疾病进展是停止 2 线治疗的最常见原因,这突出表明需要及时使用最有效的药物进行 2 线治疗,以使患者获得更长的治疗时间和延缓疾病进展。