Efficacy and safety of palbociclib plus endocrine therapy in North American women with hormone receptor-positive/human epidermal growth factor receptor 2-negative metastatic breast cancer

被引:16
作者
Gelmon, Karen A. [1 ]
Cristofanilli, Massimo [2 ]
Rugo, Hope S. [3 ]
DeMichele, Angela M. [4 ]
Joy, Anil A. [5 ]
Castrellon, Aurelio [6 ]
Sleckman, Bethany [7 ]
Mori, Ave [8 ]
Theall, Kathy Puyana [9 ]
Lu, Dongrui R. [10 ]
Huang, Xin [11 ]
Bananis, Eustratios [11 ]
Finn, Richard S. [12 ]
Slamon, Dennis J. [12 ]
机构
[1] BC Canc, 600 West 10th Ave, Vancouver, BC V5Z 4E6, Canada
[2] Northwestern Univ, Robert H Lurie Canc Ctr, Feinberg Sch Med, Chicago, IL 60611 USA
[3] Univ Calif San Francisco Helen, Diller Family Comprehens Canc Ctr, San Francisco, CA USA
[4] Univ Penn, Abramson Canc Ctr, Philadelphia, PA 19104 USA
[5] Univ Alberta, Cross Canc Inst, Edmonton, AB, Canada
[6] Mem Healthcare Syst, Breast Canc Ctr, Hollywood, FL USA
[7] Mercy Hosp St Louis, St Louis, MO USA
[8] Pfizer Oncol, Milan, Italy
[9] Pfizer Oncol, Cambridge, MA USA
[10] Pfizer Inc, La Jolla, CA USA
[11] Pfizer Oncol, New York, NY USA
[12] Univ Calif Los Angeles, David Geffen Sch Med, Santa Monica, CA USA
关键词
CDK4; 6; inhibitor; metastatic breast cancer; North America; palbociclib; LETROZOLE;
D O I
10.1111/tbj.13516
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Palbociclib is a cyclin-dependent kinase 4/6 inhibitor indicated for treatment of hormone receptor-positive/human epidermal growth factor receptor 2-negative advanced breast cancer in combination with endocrine therapy. We investigated the efficacy and safety of palbociclib in patients enrolled in North America during two-phase 3 trials: PALOMA-2 (n = 267, data cutoff: May 31, 2017) and PALOMA-3 (n = 240, data cutoffs: April 13, 2018, for overall survival, October 23, 2015, for all other outcomes). In PALOMA-2, treatment-naive postmenopausal patients with advanced breast cancer were randomized 2:1 to palbociclib (125 mg/d; 3 weeks on/1 week off [3/1]) plus letrozole (2.5 mg/d, continuous) or placebo plus letrozole. In PALOMA-3, patients who progressed on prior endocrine therapy were randomized 2:1 to palbociclib (125 mg/d; 3/1) plus fulvestrant (500 mg, per standard of care) or placebo plus fulvestrant; pre/perimenopausal patients received ovarian suppression with goserelin. Palbociclib plus endocrine therapy prolonged median progression-free survival vs placebo plus endocrine therapy in North American patients (PALOMA-2: 25.4 vs 13.7 months, hazard ratio, 0.54 [95% CI, 0.40-0.74], P PALOMA-3: 9.9 vs 3.5 months, hazard ratio, 0.52 [95% CI, 0.38-0.72], P < .0001). Objective response and clinical benefit response rates were greater with palbociclib vs placebo in North American patients in both trials. While overall survival data are not yet mature for PALOMA-2, median overall survival was increased in PALOMA-3 (32.0 vs 24.7 months, hazard ratio, 0.75 [95% CI, 0.53-1.04]), though this did not reach statistical significance (P = .0869). Safety profiles in North American patients were similar to those of the overall populations; neutropenia was the most common treatment-emergent adverse event. No new safety signals were observed. In summary, palbociclib plus endocrine therapy is an effective treatment option for North American women with hormone receptor-positive/human epidermal growth factor receptor 2-negative advanced breast cancer.
引用
收藏
页码:368 / 375
页数:8
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