Calcitriol in Combination Therapy for Prostate Cancer: Pharmacokinetic and Pharmacodynamic Interactions

被引:31
作者
Ben-Eltriki, Mohamed [1 ,2 ]
Deb, Subrata [4 ]
Guns, Emma S. Tomlinson [1 ,3 ]
机构
[1] Vancouver Gen Hosp, Vancouver Prostate Ctr, 2660 Oak St, Vancouver, BC V6H 3Z6, Canada
[2] Univ British Columbia, Dept Expt Med, Vancouver, BC V5Z 1M9, Canada
[3] Univ British Columbia, Dept Urol Sci, Vancouver, BC V5Z 1M9, Canada
[4] Roosevelt Univ, Coll Pharm, Dept Biopharmaceut Sci, Schaumburg, IL USA
关键词
Calcitriol; prostate cancer; pharmacokinetics; CYP enzymes; metabolism; pharmacodynamics; vitamin D receptor; VITAMIN-D-RECEPTOR; HIGH-DOSE CALCITRIOL; PHASE-II TRIAL; CELL-LINE LNCAP; 1-ALPHA; 25-DIHYDROXYVITAMIN D-3; ANTITUMOR-ACTIVITY; GROWTH-INHIBITION; 1,25-DIHYDROXYVITAMIN D-3; IN-VITRO; ANTICANCER ACTIVITY;
D O I
10.7150/jca.13470
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Epidemiological studies indicate that vitamin D insufficiency could have an etiological role in prostate cancer. In addition, calcitriol, used in combination with currently available drugs, has the potential to potentiate their anticancer effects or act synergistically by inhibiting distinct mechanisms involved in prostate cancer growth. Clinical data have not yet provided sufficient evidence to demonstrate benefit of vitamin D due to the limited and underpowered studies that have been published to date. Here, we review the preclinical and clinical studies that describe the activity of calcitriol, applied either alone or in combination and assessed the mechanistic basis of pharmacodynamic and pharmacokinetic interactions with calcitriol. Important considerations for calcitriol use in combination therapy with respect to safety and clinical outcomes have been discussed. Many of these combinations have therapeutic potential for the treatment of several cancer types and it is anticipated that future clinical research will put emphasis on well-designed clinical trials to establish efficacy.
引用
收藏
页码:391 / 407
页数:17
相关论文
共 134 条
[1]   Calcitriol (1,25-dihydroxycholecalciferol) potentiates activity of mitoxantrone/dexamethasone in an androgen independent prostate cancer model [J].
Ahmed, S ;
Johnson, CS ;
Rueger, RM ;
Trump, DL .
JOURNAL OF UROLOGY, 2002, 168 (02) :756-761
[2]   Expression of VDR and CYP24A1 mRNA in human tumors [J].
Anderson, MG ;
Nakane, M ;
Ruan, XA ;
Kroeger, PE ;
Wu-Wong, JR .
CANCER CHEMOTHERAPY AND PHARMACOLOGY, 2006, 57 (02) :234-240
[3]  
[Anonymous], CLIN GENITOURIN CANC
[4]   Recommended intakes of vitamin D to optimise health, associated circulating 25-hydroxyvitamin D concentrations, and dosing regimens to treat deficiency: workshop report and overview of current literature [J].
Balvers, Michiel G. J. ;
Brouwer-Brolsma, Elske M. ;
Endenburg, Silvia ;
de Groot, Lisette C. P. G. M. ;
Kok, Frans J. ;
Gunnewiek, Jacqueline Klein .
JOURNAL OF NUTRITIONAL SCIENCE, 2015, 4
[5]   Growth inhibition and differentiation in human prostate carcinoma cells induced by the vitamin D analog 1α,24-dihydroxyvitamin D2 [J].
Bauer, JA ;
Thompson, TA ;
Church, DR ;
Ariazi, EA ;
Wilding, G .
PROSTATE, 2003, 55 (03) :159-167
[7]   High-dose calcitriol and carboplatin in metastatic androgen-independent prostate cancer [J].
Beer, TM ;
Garzotto, M ;
Katovic, NM .
AMERICAN JOURNAL OF CLINICAL ONCOLOGY-CANCER CLINICAL TRIALS, 2004, 27 (05) :535-541
[8]   Weekly high-dose calcitriol and docetaxel in metastatic androgen-independent prostate cancer [J].
Beer, TM ;
Eilers, KM ;
Garzotto, M ;
Egorin, MJ ;
Lowe, BA ;
Henner, WD .
JOURNAL OF CLINICAL ONCOLOGY, 2003, 21 (01) :123-128
[9]  
Beer TM, 2001, SEMIN ONCOL, V28, P49, DOI 10.1016/S0093-7754(01)90155-1
[10]   Intermittent chemotherapy in patients with metastatic androgen-independent prostate cancer - Results from ASCENT, a double-blinded, randomized comparison of high-dose calcitriol plus docetaxel with placebo plus docetaxel [J].
Beer, Tomasz M. ;
Ryan, Christopher W. ;
Venner, Peter M. ;
Petrylak, Daniel R. ;
Chatta, Gurkamal S. ;
Ruether, J. Dean ;
Chi, Kim N. ;
Young, James ;
Henner, W. David .
CANCER, 2008, 112 (02) :326-330