117892The First Affiliated Hospital of Xiamen University, School of Medicine, Xiamen University, Xiamen, Fujian, China.
Technol Cancer Res Treat. 2022 Jan-Dec;21:15330338221132926. doi: 10.1177/15330338221132926.
Palbociclib is the most widely used cyclin-dependent kinase 4/6 inhibitor in China, but its early application efficacy on Chinese metastatic breast cancer (MBC) patients was reported deficiently. Between February 2019 to December 2021, 95 female hormone receptor-positive (HR+)/human epidermal growth factor receptor-2 negative (HER2-) patients with MBC received palbociclib combined with AI or fulvestrant were retrospectively analyzed in our center. The primary outcome was progression-free survival (PFS). The objective response rate and clinical benefit rate (CBR) were evaluated. The median follow-up period was 15 months (range from 2 to 37). Palbociclib performed superiorly when applicated in first-and-second line therapy than in later lines ( = .002). Palbociclib combined with AI or fulvestrant had a median PFS of 34 months (95% confidence interval [CI] = 6.87-61.13) and 12 months (95%CI = 7.76-16.24), respectively. Univariate subgroup analysis showed that the previous history of salvage chemotherapy ( = .015) and the presence of liver metastases ( < .001) significantly affected the efficacy of palbociclib. Despite the existence of liver metastases and primary endocrine resistance, which are two independent predictors of poor prognosis, early application of palbociclib in advanced stage can bring further benefits to these two groups of patients, rather than choosing salvage chemotherapy in the first place. Palbociclib combined with endocrine therapy has a favorable efficacy and acceptable toxicity in HR+/HER2- Chinese MBC patients. Better performance can be seen when palbociclib was applicated in the early stage.
帕博西尼是中国应用最广泛的细胞周期蛋白依赖性激酶 4/6 抑制剂,但在中国转移性乳腺癌(MBC)患者中的早期应用效果报道不足。2019 年 2 月至 2021 年 12 月,我们中心回顾性分析了 95 例激素受体阳性(HR+)/人表皮生长因子受体 2 阴性(HER2-)MBC 女性患者,接受帕博西尼联合 AI 或氟维司群治疗。主要结局是无进展生存期(PFS)。评估客观缓解率和临床获益率(CBR)。中位随访时间为 15 个月(范围 2-37 个月)。帕博西尼在一线和二线治疗中优于后线治疗( = .002)。帕博西尼联合 AI 或氟维司群的中位 PFS 分别为 34 个月(95%置信区间 [CI] = 6.87-61.13)和 12 个月(95%CI = 7.76-16.24)。单因素亚组分析显示,既往挽救性化疗史( = .015)和肝转移( < .001)显著影响帕博西尼的疗效。尽管存在肝转移和原发性内分泌耐药,这是预后不良的两个独立预测因素,但在晚期阶段早期应用帕博西尼可以为这两组患者带来进一步的获益,而不是首先选择挽救性化疗。帕博西尼联合内分泌治疗在 HR+/HER2-中国 MBC 患者中具有良好的疗效和可接受的毒性。在早期阶段应用帕博西尼时效果更好。