Goel Shom, Jovanović Bojana, Chu Xiangying, Hughes Melissa, Erick Timothy K, Russo Douglas, DiLullo Molly, Wrabel Eileen, Jeselsohn Rinath, Lin Nancy U, Tayob Nabihah, Mittendorf Elizabeth, Schnitt Stuart, Tolaney Sara M
Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
Breast Oncology Program, Dana-Farber Brigham Cancer Center, Boston, Massachusetts.
Clin Cancer Res. 2025 Apr 14;31(8):1427-1436. doi: 10.1158/1078-0432.CCR-24-2647.
Cyclin-dependent kinase 4/6 inhibitors can significantly extend survival when given in combination with endocrine therapy in patients with hormone receptor-positive metastatic breast cancer. However, their activity has been relatively underexplored in patients with metastatic triple-negative breast cancer (mTNBC).
We conducted a single-arm phase II study of abemaciclib monotherapy in patients with Rb-positive mTNBC. Patients were treated with abemaciclib 200 mg orally twice daily until disease progression, unacceptable toxicity, or withdrawal of consent. The primary endpoint was the objective response rate; secondary endpoints included progression-free survival (PFS), overall survival (OS), clinical benefit rate, disease control rate, and safety and tolerability.
A total of 27 patients were enrolled before the trial was closed early because of slow accrual. Patients had received a median of two lines of systemic therapy in the metastatic setting prior to enrollment. After a median follow-up of 28.5 months, the objective response rate was 0%, the clinical benefit rate was 14.8%, and the disease control rate was 22.2%. The median PFS was 1.94 months (95% confidence interval, 1.84-11.47), and the median OS was 8.44 months (95% confidence interval, 4.57-15.57). Median PFS and OS did not differ significantly based on androgen receptor and PD-L1 status. Pretreatment gene expression profiling of tumor tissue provided some hypothesis-generating insights into biological features associated with clinical benefit in this study. The most common treatment-related adverse events of grade 2 or higher were diarrhea (40.7%), neutropenia (40.7%), anemia (29.6%), and nausea (29.6%).
Abemaciclib monotherapy did not show clinical activity in patients with pretreated Rb-positive mTNBC.
细胞周期蛋白依赖性激酶4/6抑制剂与内分泌治疗联合应用时,可显著延长激素受体阳性转移性乳腺癌患者的生存期。然而,其在转移性三阴性乳腺癌(mTNBC)患者中的活性尚未得到充分研究。
我们开展了一项阿贝西利单药治疗Rb阳性mTNBC患者的单臂II期研究。患者口服阿贝西利200 mg,每日两次,直至疾病进展、出现不可接受的毒性或撤回知情同意。主要终点为客观缓解率;次要终点包括无进展生存期(PFS)、总生存期(OS)、临床获益率、疾病控制率以及安全性和耐受性。
由于入组缓慢,该试验提前结束,共入组27例患者。患者在入组前转移性疾病阶段接受的全身治疗中位数为2线。中位随访28.5个月后,客观缓解率为0%,临床获益率为14.8%,疾病控制率为22.2%。中位PFS为1.94个月(95%置信区间,1.84 - 11.47),中位OS为8.44个月(95%置信区间,4.57 - 15.57)。基于雄激素受体和PD-L1状态,中位PFS和OS无显著差异。肿瘤组织的治疗前基因表达谱分析为该研究中与临床获益相关的生物学特征提供了一些产生假设的见解。最常见的2级或更高等级的治疗相关不良事件为腹泻(40.7%)、中性粒细胞减少(40.7%)、贫血(29.6%)和恶心(29.6%)。
阿贝西利单药治疗在经治的Rb阳性mTNBC患者中未显示出临床活性。