Prevalence of the co-prescription of tamoxifen and CYP2D6 inhibitors in Saudi population: A cross sectional study

被引:4
作者
Arafah, Azher [1 ]
Yakout, Khalid [1 ,2 ]
Rehman, Muneeb U. [1 ]
Alsharif, Ammar Mohammed [1 ,3 ]
AlJawadi, Mohammad H. [1 ]
Al-Omar, Hussain Abdulrahman [1 ]
机构
[1] King Saud Univ, Coll Pharm, Dept Clin Pharm, POB 2457, Riyadh 11451, Saudi Arabia
[2] AlMaarefa Univ, Coll Pharm, POB 71666, Riyadh 11597, Saudi Arabia
[3] SERVIER Saudi Arabia, POB 112744, Jeddah 21371, Saudi Arabia
关键词
Adherence; Breast cancer; CYP2D6; inhibitor; Tamoxifen; BREAST-CANCER; ENDOCRINE THERAPY; HOT FLUSHES; ADHERENCE; WOMEN; MORTALITY;
D O I
10.1016/j.jsps.2020.02.004
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Consumption of Cytochrome P450 2D6 (CYP2D6) inhibiting drugs along with tamoxifen treatment results in decrease in plasma concentration of endoxifen, the major active tamoxifen metabolite. Simultaneous use of CYP2D6 inhibitors, such as selective serotonin reuptake inhibitors (SSIs), as well as lesser tamoxifen adherence may negatively impact tamoxifen efficacy in patients with breast cancer. The objective of our study was to assess the co-prescription of CYP2D6 inhibitors and tamoxifen use and also to relate concomitant CYP2D6 inhibitor use and tamoxifen adherence to breast cancer in Riyadh, Saudi Arabia. All patients treated for breast cancer who had at least one tamoxifen prescription in their electronic medical records (EMRs) from June 2015 to June 2017 were included. Patients who had other adjuvant hormonal therapy were excluded from the study. In total, 499 patients (25 males and 474 females) with breast cancer using tamoxifen were included. Our study was purely observational study revealed that prescription of weak inhibitors with tamoxifen increased in the second year as opposed to decrease in the prescription of strong inhibitors. Also, a substantial percentage of patient population were found to be non-adherent to the tamoxifen therapy in this study. (C) 2020 The Author(s). Published by Elsevier B.V. on behalf of King Saud University.
引用
收藏
页码:440 / 444
页数:5
相关论文
共 33 条
[1]   Protein expression profile and prevalence pattern of the molecular classes of breast cancer - a Saudi population based study [J].
Al Tamimi, Dalal M. ;
Shawarby, Mohamed A. ;
Ahmed, Ayesha ;
Hassan, Ammar K. ;
AlOdaini, Amal A. .
BMC CANCER, 2010, 10
[2]  
ALOTAIBI RHR, 2018, PLOSONE, V22
[3]   Determinants of breast cancer in Saudi women from Makkah region: a case-control study (breast cancer risk factors among Saudi women) [J].
Alsolami, Fatmah J. ;
Azzeh, Firas S. ;
Ghafouri, Khloud J. ;
Ghaith, Mazen M. ;
Almaimani, Riyad A. ;
Almasmoum, Hussain A. ;
Abdulal, Rwaa H. ;
Abdulaal, Wesam H. ;
Jazar, Abdelelah S. ;
Tashtoush, Sufyan H. .
BMC PUBLIC HEALTH, 2019, 19 (01)
[4]   Estrogen receptor breast cancer phenotypes in the surveillance, epidemiology, and end results database [J].
Anderson, WF ;
Chatterjee, N ;
Ershler, WB ;
Brawley, OW .
BREAST CANCER RESEARCH AND TREATMENT, 2002, 76 (01) :27-36
[5]   Incidence of Breast Cancer in the United States: Current and Future Trends [J].
Anderson, William F. ;
Katki, Hormuzd A. ;
Rosenberg, Philip S. .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2011, 103 (18) :1397-1402
[6]  
Anghel Laura Alexandra, 2019, Med Pharm Rep, V92, P117, DOI 10.15386/mpr-1201
[7]  
[Anonymous], MEDICAL GENETICS SUM
[8]   Unjustified prescribing of CYP2D6 inhibiting SSRIs in women treated with tamoxifen [J].
Binkhorst, Lisette ;
Mathijssen, Ron H. J. ;
van Herk-Sukel, Myrthe P. P. ;
Bannink, Marjolein ;
Jager, Agnes ;
Wiemer, Erik A. C. ;
van Gelder, Teun .
BREAST CANCER RESEARCH AND TREATMENT, 2013, 139 (03) :923-929
[9]   Tamoxifen ('Nolvadex'): a review [J].
Clemons, M ;
Danson, S ;
Howell, A .
CANCER TREATMENT REVIEWS, 2002, 28 (04) :165-180
[10]   Managing menopausal symptoms and depression in tamoxifen users Implications of drug and medicinal interactions [J].
Desmarais, Julie Eve ;
Looper, Karl J. .
MATURITAS, 2010, 67 (04) :296-308