Department of Medical Oncology, State Key Laboratory of Oncology in South China, Guangdong Provincial Clinical Research Center for Cancer, Sun Yat-sen University Cancer Center, No. 651, Dongfeng Road East, Yuexiu District, Guangzhou, 510060, China.
Affiliated Cancer Hospital of Guangxi Medical University, Nanning, 530021, China.
BMC Cancer. 2024 Sep 30;24(1):1214. doi: 10.1186/s12885-024-12953-9.
Pre-clinical data suggests a potential synergistic effect of eribulin and platinum. However, clinical data on the combination for metastatic breast cancer (mBC) is lacking. We evaluated the efficacy and safety of eribulin plus carboplatin (ErCb) in patients with mBC.
This multicenter, real-world cohort study included patients with pre-treated metastatic triple negative breast cancer (TNBC) or endocrine-refractory hormone receptor (HR) positive, HER2-negative mBC who received ErCb. Eribulin (1.4 mg/m2) and carboplatin (target AUC = 2) were administered intravenously on day 1 and 8 of 21-day cycle. Objective response rate (ORR), disease control rate (DCR), progression-free survival (PFS), overall survival (OS), and adverse events (AEs) were evaluated.
From March 2022 to December 2023, a cohort of 37 patients were recruited to the study. Among them, 22 patients have TNBC and 15 have HR + HER2 - mBC. Of the 22 patients with TNBC, 8 had an initial diagnosis of the HR + HER2 - subtype. The median treatment was 6 cycles (range, 2 - 8 cycles). In the full cohort, TNBC, and HR + HER2 - subgroup, the ORR were 51.4%, 54.5% and 46.7%, the DCR were 81.1%, 81.8% and 80%, and the median PFS were 5 months, 5 months, and 5.2 months, respectively. The median OS was 12.7 months in the entire cohort and 12.8 months in TNBC subgroup. The most common grade 3/4 hematological AEs were neutropenia (37.8%), leukopenia (35.1%), febrile neutropenia (10.8%), thrombocytopenia (5.4%), and anemia (2.7%). No grade 3/4 non-hematological AEs were observed.
ErCb demonstrated favorable efficacy and tolerability in patients with heavily pre-treated mBC, especially TNBC. The findings of the current study warrant further investigation of the application of this combination in earlier lines of mBC treatment.
临床前数据表明,表柔比星与顺铂联合具有潜在的协同作用。然而,转移性乳腺癌(mBC)中联合应用这两种药物的临床数据尚缺乏。我们评估了表柔比星联合卡铂(ErCb)治疗 mBC 患者的疗效和安全性。
这是一项多中心、真实世界的队列研究,纳入了接受过治疗的转移性三阴性乳腺癌(TNBC)或内分泌难治性激素受体(HR)阳性、HER2 阴性 mBC 患者,这些患者接受了 ErCb 治疗。表柔比星(1.4mg/m2)和顺铂(目标 AUC=2)于 21 天周期的第 1 天和第 8 天静脉输注。评估客观缓解率(ORR)、疾病控制率(DCR)、无进展生存期(PFS)、总生存期(OS)和不良反应(AE)。
从 2022 年 3 月至 2023 年 12 月,该研究共纳入 37 例患者。其中,22 例患者为 TNBC,15 例为 HR+HER2- mBC。在 22 例 TNBC 患者中,有 8 例最初诊断为 HR+HER2-亚型。中位治疗周期数为 6 个(范围:2-8 个)。在全队列、TNBC 和 HR+HER2-亚组中,ORR 分别为 51.4%、54.5%和 46.7%,DCR 分别为 81.1%、81.8%和 80%,中位 PFS 分别为 5 个月、5 个月和 5.2 个月,中位 OS 分别为 12.7 个月和 12.8 个月。最常见的 3/4 级血液学不良反应为中性粒细胞减少症(37.8%)、白细胞减少症(35.1%)、发热性中性粒细胞减少症(10.8%)、血小板减少症(5.4%)和贫血(2.7%)。未观察到 3/4 级非血液学不良反应。
ErCb 对治疗既往治疗后转移性乳腺癌(mBC),特别是 TNBC 患者具有良好的疗效和耐受性。本研究结果支持进一步研究该联合方案在 mBC 治疗早期线中的应用。