Neven Patrick, Johnston Stephen R D, Toi Masakazu, Sohn Joohyuk, Inoue Kenichi, Pivot Xavier, Burdaeva Olga, Okera Meena, Masuda Norikazu, Kaufman Peter A, Koh Han, Grischke Eva-Maria, Conte PierFranco, Lu Yi, Haddad Nadine, Hurt Karla C, Llombart-Cussac Antonio, Sledge George W
Universitaire Ziekenhuizen Leuven, Leuven, Belgium.
The Royal Marsden NHS Foundation Trust, London, United Kingdom.
Clin Cancer Res. 2021 Nov 1;27(21):5801-5809. doi: 10.1158/1078-0432.CCR-20-4685. Epub 2021 Aug 10.
In MONARCH 2, abemaciclib plus fulvestrant significantly prolonged progression-free survival (PFS) and overall survival (OS) versus placebo plus fulvestrant in patients with hormone receptor positive (HR), HER2 advanced breast cancer. This exploratory analysis assessed the efficacy of abemaciclib plus fulvestrant across subgroups of patients receiving study therapy as first- or second-line treatment for metastatic disease.
Improvements were estimated using Cox models, and a test of interactions of subgroups with treatment was performed.
The benefit in PFS [first-line, HR, 0.57; 95% confidence interval (CI), 0.45-0.73; second-line, HR, 0.48; 95% CI, 0.36-0.64] and OS (first-line, HR, 0.85; 95% CI, 0.64-1.14; second-line, HR, 0.66; 95% CI, 0.46-0.94) was observed across both subgroups, consistent with the intent-to-treat (ITT) population. In first-line patients (abemaciclib arm, = 265; placebo arm, = 133), the numerically largest effect on PFS and OS was observed in patients with primary resistance to endocrine therapy (ET; PFS, HR, 0.40; 95% CI, 0.26-0.63; OS, HR, 0.58; 95% CI, 0.35-0.97) and visceral disease (PFS, HR, 0.54; 95% CI, 0.39-0.73; OS, HR, 0.82; 95% CI, 0.58-1.20). In second-line patients (abemaciclib arm, = 170; placebo arm, = 86), a numerical benefit in PFS and OS was observed across primary and secondary ET resistance, with numerically more pronounced effects observed in patients with visceral disease (PFS, HR, 0.39; 95% CI, 0.27-0.57; OS, HR, 0.51; 95% CI, 0.33-0.81). Prolongation of time to second disease progression, time to chemotherapy, and chemotherapy-free survival was observed in both subgroups.
Consistent with the ITT population, a benefit in PFS and OS was observed across the first- and second-line subgroups in MONARCH 2.
在MONARCH 2试验中,与安慰剂加氟维司群相比,阿贝西利联合氟维司群显著延长了激素受体阳性(HR)、HER2阴性晚期乳腺癌患者的无进展生存期(PFS)和总生存期(OS)。本探索性分析评估了阿贝西利联合氟维司群在接受研究治疗作为转移性疾病一线或二线治疗的患者亚组中的疗效。
使用Cox模型估计改善情况,并对亚组与治疗的相互作用进行检验。
在两个亚组中均观察到PFS(一线,HR = 0.57;95%置信区间[CI],0.45 - 0.73;二线,HR = 0.48;95% CI,0.36 - 0.64)和OS(一线,HR = 0.85;95% CI,0.64 - 1.14;二线,HR = 0.66;95% CI,0.46 - 0.94)的获益,与意向性治疗(ITT)人群一致。在一线患者中(阿贝西利组,n = 265;安慰剂组,n = 133),在内分泌治疗(ET)原发性耐药患者(PFS,HR = 0.40;95% CI,0.26 - 0.63;OS,HR = 0.58;95% CI,0.35 - 0.97)和内脏疾病患者(PFS,HR = 0.54;95% CI,0.39 - 0.73;OS,HR = 0.82;95% CI,0.58 - 1.20)中观察到对PFS和OS在数值上最大的疗效。在二线患者中(阿贝西利组,n = 170;安慰剂组,n = 86),在原发性和继发性ET耐药患者中均观察到PFS和OS在数值上的获益,在内脏疾病患者中观察到数值上更显著的疗效(PFS,HR = 0.39;95% CI,0.27 - 0.57;OS,HR = 0.51;95% CI,0.33 - 0.81)。在两个亚组中均观察到至第二次疾病进展时间、至化疗时间和无化疗生存期的延长。
与ITT人群一致,在MONARCH 2试验的一线和二线亚组中均观察到PFS和OS的获益。