Palbociclib has no clinically relevant effect on the QTc interval in patients with advanced breast cancer

被引:37
作者
Durairaj, Chandrasekar [1 ]
Ruiz-Garcia, Ana [1 ]
Gauthier, Eric R. [2 ]
Huang, Xin [1 ]
Lu, Dongrui R. [1 ]
Hoffman, Justin T. [1 ]
Finn, Richard S. [4 ]
Joy, Anil A. [5 ]
Ettl, Johannes [6 ]
Rugo, Hope S. [3 ]
Zheng, Jenny [1 ]
Wilner, Keith D. [1 ]
Wang, Diane D. [1 ]
机构
[1] Pfizer Inc, Global Prod Dev, San Diego, CA USA
[2] Pfizer Inc, San Diego, CA USA
[3] Univ Calif San Francisco, Dept Med, Helen Diller Family Comprehens Canc Ctr, San Francisco, CA USA
[4] Univ Calif Los Angeles, Dept Med, Div Hematol Oncol, Geffen Sch Med, Los Angeles, CA 90024 USA
[5] Univ Alberta, Cross Canc Inst, Dept Oncol, Edmonton, AB, Canada
[6] Tech Univ Munich, Right Isar Hosp, Dept Obstet & Gynecol, Munich, Germany
关键词
advanced breast cancer; concentration-QTc modeling; ECG; palbociclib; QT interval; DEPENDENT KINASE 4/6; CARDIAC REPOLARIZATION; PROLONGED QTC; RISK; COMBINATION; INHIBITOR; LETROZOLE; SAFETY; GENDER;
D O I
10.1097/CAD.0000000000000589
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The aim of this study was to assess the potential effects of palbociclib in combination with letrozole on QTc. PALOMA-2, a phase 3, randomized, double-blind, placebo-controlled trial, compared palbociclib plus letrozole with placebo plus letrozole in postmenopausal women with estrogen receptor-positive, human epidermal growth factor receptor 2-negative advanced breast cancer. The study included a QTc evaluation substudy carried out as a definitive QT interval prolongation assessment for palbociclib. Time-matched triplicate ECGs were performed at 0, 2, 4, 6, and 8h at baseline (Day 0) and on Cycle 1 Day 14. Additional ECGs were collected from all patients for safety monitoring. The QT interval was corrected for heart rate using Fridericia's correction (QTcF), Bazett's correction (QTcB), and a study-specific correction factor (QTcS). In total, 666 patients were randomized 2:1 to palbociclib plus letrozole or placebo plus letrozole. Of these, 125 patients were enrolled in the QTc evaluation substudy. No patients in the palbociclib plus letrozole arm of the substudy (N=77) had a maximum postbaseline QTcS or QTcF value of 480ms, or a maximum increase from clock time-matched baseline for QTcS or QTcF values of 60ms. The upper bounds of the one-sided 95% confidence interval for the mean change from time-matched baseline for QTcS, QTcF, and QTcB at all time points and at steady-state C-max following repeated administration of 125mg palbociclib were less than 10ms. Palbociclib, when administered with letrozole at the recommended therapeutic dosing regimen, did not prolong the QT interval to a clinically relevant extent.
引用
收藏
页码:271 / 280
页数:10
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