-
Je něco špatně v tomto záznamu ?
Contribution of ABCB1 and CYP2D6 genotypes to the outcome of tamoxifen adjuvant treatment in premenopausal women with breast cancer
S. Argalácsová, O. Slanař, P. Vítek, P. Tesařová, H. Bakhouche, M. Dražďáková, O. Bartošová, T. Zima, L. Petruželka
Jazyk angličtina Země Česko
Typ dokumentu časopisecké články, práce podpořená grantem
NLK
Directory of Open Access Journals
od 1991
Free Medical Journals
od 1998
ProQuest Central
od 2005-01-01
Medline Complete (EBSCOhost)
od 2006-01-01
Nursing & Allied Health Database (ProQuest)
od 2005-01-01
Health & Medicine (ProQuest)
od 2005-01-01
ROAD: Directory of Open Access Scholarly Resources
od 1998
- MeSH
- adjuvantní chemoterapie MeSH
- cytochrom P-450 CYP2D6 genetika MeSH
- dospělí MeSH
- genotyp MeSH
- hormonální protinádorové látky aplikace a dávkování MeSH
- lidé středního věku MeSH
- lidé MeSH
- nádory prsu farmakoterapie genetika MeSH
- P-glykoproteiny genetika MeSH
- premenopauza účinky léků genetika MeSH
- tamoxifen aplikace a dávkování MeSH
- výsledek terapie MeSH
- Check Tag
- dospělí MeSH
- lidé středního věku MeSH
- lidé MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
Recent pre-clinical evidence suggests that the active metabolite of tamoxifen, endoxifen, is a substrate for efflux pump P-glycoprotein. The aim of our study was to evaluate, if the polymoprhisms within ABCB1 gene alter tamoxifen adjuvant treatment efficacy in premenopausal women. Totally 71 premenopausal women with estrogen receptor positive breast cancer indicated for tamoxifen adjuvant treatment were followed retrospectively for median period of 56 months. The gentic polymorphisms of CYP2D6 and ABCB1 were analyzed and potential covariates as tumor grading, staging, age at the diagnosis, comedication, quantitative positivity of ER or PR were also evaluated. Cox proportional-hazards regression model indicated that patients carrying at least one variant allele in ABCB1 rs1045642 had significantly longer time to event survival compared to wild type subjects. Non-significant trend was noted for better treatment outcome of patients carrying at least one variant allele in the SNP rs2032582, while for the CYP2D6 polymorphism poor metabolizer phenotype resulted in worse outcome in comparison to extensive metabolizers subjects with HR of 4.04 (95 % CI 0.31-52.19). Similarly, patients using CYP2D6 inhibitors had non-significantly shorter time-to-event as compared to never users resulting in hazard ratio of 2.06 (95 % CI 0.40-10.63). ABCB1 polymorphisms may affect outcome of tamoxifen adjuvant treatment in premenopausal breast cancer patiens. This factor should be taken into account in addition to the CYP2D6 polymorphism or phenotypic inhibition of CYP2D6 activity.
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc16031169
- 003
- CZ-PrNML
- 005
- 20241120093208.0
- 007
- ta
- 008
- 161101s2015 xr d f 000 0|ENG||
- 009
- AR
- 024 7_
- $a 10.33549/physiolres.933234 $2 doi
- 035 __
- $a (PubMed)26681084
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a ENG
- 044 __
- $a xr
- 100 1_
- $a Argalácsová, Soňa $u Department of Oncology, First Faculty of Medicine, Charles University and General Teaching Hospital, Prague, Czech Republic; Institute of Pharmacology, First Faculty of Medicine, Charles University and General Teaching Hospital, Prague, Czech Republic $7 xx0144657
- 245 10
- $a Contribution of ABCB1 and CYP2D6 genotypes to the outcome of tamoxifen adjuvant treatment in premenopausal women with breast cancer / $c S. Argalácsová, O. Slanař, P. Vítek, P. Tesařová, H. Bakhouche, M. Dražďáková, O. Bartošová, T. Zima, L. Petruželka
- 520 9_
- $a Recent pre-clinical evidence suggests that the active metabolite of tamoxifen, endoxifen, is a substrate for efflux pump P-glycoprotein. The aim of our study was to evaluate, if the polymoprhisms within ABCB1 gene alter tamoxifen adjuvant treatment efficacy in premenopausal women. Totally 71 premenopausal women with estrogen receptor positive breast cancer indicated for tamoxifen adjuvant treatment were followed retrospectively for median period of 56 months. The gentic polymorphisms of CYP2D6 and ABCB1 were analyzed and potential covariates as tumor grading, staging, age at the diagnosis, comedication, quantitative positivity of ER or PR were also evaluated. Cox proportional-hazards regression model indicated that patients carrying at least one variant allele in ABCB1 rs1045642 had significantly longer time to event survival compared to wild type subjects. Non-significant trend was noted for better treatment outcome of patients carrying at least one variant allele in the SNP rs2032582, while for the CYP2D6 polymorphism poor metabolizer phenotype resulted in worse outcome in comparison to extensive metabolizers subjects with HR of 4.04 (95 % CI 0.31-52.19). Similarly, patients using CYP2D6 inhibitors had non-significantly shorter time-to-event as compared to never users resulting in hazard ratio of 2.06 (95 % CI 0.40-10.63). ABCB1 polymorphisms may affect outcome of tamoxifen adjuvant treatment in premenopausal breast cancer patiens. This factor should be taken into account in addition to the CYP2D6 polymorphism or phenotypic inhibition of CYP2D6 activity.
- 650 _2
- $a dospělí $7 D000328
- 650 _2
- $a hormonální protinádorové látky $x aplikace a dávkování $7 D018931
- 650 _2
- $a nádory prsu $x farmakoterapie $x genetika $7 D001943
- 650 _2
- $a adjuvantní chemoterapie $7 D017024
- 650 _2
- $a cytochrom P-450 CYP2D6 $x genetika $7 D019389
- 650 _2
- $a ženské pohlaví $7 D005260
- 650 _2
- $a genotyp $7 D005838
- 650 _2
- $a lidé $7 D006801
- 650 _2
- $a lidé středního věku $7 D008875
- 650 _2
- $a P-glykoproteiny $x genetika $7 D018435
- 650 _2
- $a premenopauza $x účinky léků $x genetika $7 D017697
- 650 _2
- $a tamoxifen $x aplikace a dávkování $7 D013629
- 650 _2
- $a výsledek terapie $7 D016896
- 655 _2
- $a časopisecké články $7 D016428
- 655 _2
- $a práce podpořená grantem $7 D013485
- 700 1_
- $a Slanař, Ondřej $7 xx0058262 $u Institute of Pharmacology, First Faculty of Medicine, Charles University and General Teaching Hospital, Prague, Czech Republic; Institute of Clinical Biochemistry and Laboratory Diagnostics, First Faculty of Medicine, Charles University and General Teaching Hospital, Prague, Czech Republic
- 700 1_
- $a Vítek, Pavel, $d 1960- $7 mzk2006322806 $u Institute of Radiotherapy, First Faculty of Medicine, Charles University and Hospital Na Bulovce, Prague, Czech Republic
- 700 1_
- $a Tesařová, Petra, $d 1961- $7 xx0102804 $u Department of Oncology, First Faculty of Medicine, Charles University and General Teaching Hospital, Prague, Czech Republic
- 700 1_
- $a Bakhouche, Hana $7 xx0324719 $u Institute of Pharmacology, First Faculty of Medicine, Charles University and General Teaching Hospital, Prague, Czech Republic
- 700 1_
- $a Dražďáková, Marcela $7 xx0075797 $u Institute of Clinical Biochemistry and Laboratory Diagnostics, First Faculty of Medicine, Charles University and General Teaching Hospital, Prague, Czech Republic
- 700 1_
- $a Bartošová, Olga $7 mzk2016928814 $u Institute of Pharmacology, First Faculty of Medicine, Charles University and General Teaching Hospital, Prague, Czech Republic
- 700 1_
- $a Zima, Tomáš, $d 1966- $7 jn20000620440 $u Institute of Clinical Biochemistry and Laboratory Diagnostics, First Faculty of Medicine, Charles University and General Teaching Hospital, Prague, Czech Republic
- 700 1_
- $a Petruželka, Luboš, $d 1952- $7 jn19990209650 $u Department of Oncology, First Faculty of Medicine, Charles University and General Teaching Hospital, Prague, Czech Republic
- 773 0_
- $w MED00003824 $t Physiological research $x 1802-9973 $g Roč. 64, Suppl 4 (2015), s. S539-S547
- 773 0_
- $t Prof. Jaroslav Květina celebrates his 85th birthday $g (2015), s. S539-S547 $w MED00191412
- 856 41
- $u http://www.biomed.cas.cz/physiolres/ $y domovská stránka časopisu
- 910 __
- $a ABA008 $b A 4120 $c 266 $y 4 $z 0
- 990 __
- $a 20161101 $b ABA008
- 991 __
- $a 20241120093203 $b ABA008
- 999 __
- $a ok $b bmc $g 1173609 $s 955827
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2015 $b 64 $c Suppl 4 $d S539-S547 $i 1802-9973 $m Physiological research $n Physiol. Res. (Print) $x MED00003824
- BMC ##
- $a 2015 $d S539-S547 $m Prof. Jaroslav Květina celebrates his 85th birthday $x MED00191412
- LZP __
- $b NLK118 $a Pubmed-20161101