Mehta Sandhya, Kwong Jackie, Lam Clara, Feinberg Bruce
Daiichi Sankyo, Basking Ridge, NJ, United States.
Johnson & Johnson, New Brunswick, NJ, United States.
Oncologist. 2025 Jun 4;30(6). doi: 10.1093/oncolo/oyaf106.
Hormonal therapy (HT) based regimen is the preferred first-line (1L) treatment for hormone receptor-positive (HR+) metastatic breast cancer (mBC) with human receptor epidermal growth factor 2 (HER2)-low expression. However, HT resistance frequently emerges with many receiving subsequent chemotherapy (CT). This study aimed to examine CT treatment patterns and outcomes among patients with HR+/HER2-low mBC.
Patient characteristics and clinical data of adults receiving CT for HR+/HER2-low mBC were collected via physician-abstracted chart review from 10/1/2021 to 1/31/2022. Data were summarized using descriptive statistics with the Kaplan-Meier method to estimate time-to-event outcomes. Statistical comparisons were conducted between patients who received 1L CT vs CT after HT-based regimens (any line).
Two hundred and twenty three HR+/HER2-low patients were included, and CT utilization was described by line within metastatic setting: 1L = 20.2% (n = 45), 2L 26.4% (n = 59), 3L+ = 53.4% (n = 119). A higher rate of visceral metastases (86.7% vs 65.7%, P = .01) and lower Eastern Cooperative Oncology Group (ECOG) score (88.9% vs 70.2%, P = 0.01) were associated with 1L CT vs CT post-HT-based treatment. The median time-to-treatment discontinuation (TTD) and real-world progression free survival (rwPFS) of CT were similar between the groups (TTD: 6.7 months vs 8.3 months for the 1L CT and CT post-HT-based regimen groups, respectively, P = .13; rwPFS: 9.3 months vs 8.8 months, P = .26).
In this sample of HR+/HER2-low mBC patients, most patients switched to CT after two lines of therapy with a median rwPFS shorter than 10 months. The findings highlight unmet needs for a more effective targeted therapeutic alternative to CT for HR+/HER2-low mBC patients.
基于激素疗法(HT)的方案是激素受体阳性(HR+)、人表皮生长因子受体2(HER2)低表达的转移性乳腺癌(mBC)的首选一线(1L)治疗方法。然而,HT耐药经常出现,许多患者随后接受化疗(CT)。本研究旨在研究HR+/HER2低表达mBC患者的CT治疗模式和结局。
通过医生提取病历回顾,收集了2021年10月1日至2022年1月31日接受CT治疗的HR+/HER2低表达mBC成人患者的特征和临床数据。数据采用描述性统计和Kaplan-Meier方法进行总结,以估计事件发生时间结局。对接受1L CT与基于HT方案后的CT(任何线)的患者进行了统计比较。
纳入了223例HR+/HER2低表达患者,并按转移阶段的线描述了CT的使用情况:1L = 20.2%(n = 45),2L = 26.4%(n = 59),3L及以上 = 53.4%(n = 119)。与基于HT治疗后的CT相比,1L CT与更高的内脏转移率(86.7%对65.7%,P = 0.01)和更低的东部肿瘤协作组(ECOG)评分(88.9%对70.2%,P = 0.01)相关。两组之间CT的中位治疗中断时间(TTD)和真实世界无进展生存期(rwPFS)相似(TTD:1L CT组和基于HT方案后的CT组分别为6.7个月和8.3个月,P = 0.13;rwPFS:9.3个月对8.8个月,P = 0.26)。
在这个HR+/HER2低表达mBC患者样本中,大多数患者在两线治疗后改用CT,中位rwPFS短于10个月。这些发现凸显了HR+/HER2低表达mBC患者对比CT更有效的靶向治疗替代方案的未满足需求。