Reproductive and developmental toxicity assessment of palbociclib, a CDK4/6 inhibitor, in Sprague-Dawley rats and New Zealand White rabbits

被引:16
|
作者
Catlin, N. R. [1 ]
Bowman, C. J. [1 ]
Engel, S. M. [1 ]
Sacaan, A. [3 ]
Thibault, S. [3 ]
Lewis, E. M. [2 ]
Cappon, G. D. [1 ]
机构
[1] Pfizer, Groton, CT USA
[2] Chalk River Labs Inc, Safety Assessment, Horsham, PA USA
[3] Pfizer, La Jolla, CA USA
关键词
Palbociclib; CDK4/6; Embryo-fetal development; Fertility; Rat; Rabbit; CYCLIN D; DEFICIENT; MICE;
D O I
10.1016/j.reprotox.2019.07.016
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Palbociclib is a selective inhibitor of the cyclin-dependent kinase (CDK) 4/6, approved for the treatment of breast cancer. We assessed the potential effects of oral administration of palbociclib on reproduction and development. There were no effects on female or male fertility indices; however, in the male there was seminiferous tubule degeneration in the testes and secondary findings in the epididymides, lower testicular and epididymal weights, sperm density and motility. Palbociclib was not teratogenic in rats or rabbits; however, in the presence of maternal toxicity (lower maternal body weight gain and food consumption), low fetal body weights were observed in rats and small forepaw phalanges were noted in rabbits. There were, however, no adverse effects on the F1 generation in a pre- and post-natal developmental toxicity study in the rat.
引用
收藏
页码:76 / 84
页数:9
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