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Published in: Breast Cancer Research and Treatment 3/2018

01-10-2018 | Clinical trial

CYP2D6 genotype and endoxifen plasma concentration do not predict hot flash severity during tamoxifen therapy

Authors: Laura E. Jansen, Wendy A. Teft, Rhiannon V. Rose, Daniel J. Lizotte, Richard B. Kim

Published in: Breast Cancer Research and Treatment | Issue 3/2018

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Abstract

Purpose

Tamoxifen is frequently prescribed to prevent breast cancer recurrence. Tamoxifen is a prodrug and requires bioactivation by CYP2D6. Tamoxifen use is often limited by adverse effects including severe hot flashes. There is paucity of prospectively collected data in terms of CYP2D6 genotype and measured tamoxifen, 4-hydroxytamoxifen and endoxifen concentrations in relation to hot flash severity during tamoxifen therapy.

Methods

We conducted a longitudinal prospective study of breast cancer patients on tamoxifen (n = 410). At each visit, blood samples were collected, and patients completed a standardized hot flash survey (n = 1144) that reflected hot flash severity during the 7 days prior to the visit. Plasma concentrations of tamoxifen, 4-hydroxytamoxifen, and endoxifen were measured using liquid chromatography-tandem mass spectrometry and genotyping was carried out for CYP2D6. A linear mixed-effects regression analysis assessed the association of covariates in relation to the hot flash severity score (HFSS).

Results

Median age at first assessment was 50 years with 61.9% of patients considered peri-menopausal. Most patients (92.2%) experienced hot flash symptoms with 51.0% having low HFSS (0–4) and 7.32% experiencing HFSS > 25. Age was significantly associated with hot flash severity, with patients aged 45–59 more likely to have higher HFSS. Neither duration of tamoxifen therapy nor observed tamoxifen, endoxifen and 4-hydroxy tamoxifen plasma concentration predicted hot flash severity. Genetic variation in CYP2D6 or CYP3A4 was not predictive of hot flash severity.

Conclusions

Hot flash severity during tamoxifen therapy can not be accounted for by CYP2D6 genotype or observed plasma concentration of tamoxifen, 4-hydroxytamoxifen, or endoxifen.
Literature
1.
go back to reference Ahern TP, Hertz DL, Damkier P et al (2017) Cytochrome P-450 2D6 (CYP2D6) Genotype and breast cancer recurrence in tamoxifen-treated patients: evaluating the importance of loss of heterozygosity. Am J Epidemiol 185:75–85CrossRefPubMedPubMedCentral Ahern TP, Hertz DL, Damkier P et al (2017) Cytochrome P-450 2D6 (CYP2D6) Genotype and breast cancer recurrence in tamoxifen-treated patients: evaluating the importance of loss of heterozygosity. Am J Epidemiol 185:75–85CrossRefPubMedPubMedCentral
2.
go back to reference Hawse JR, Subramaniam M, Cicek M et al (2013) Endoxifen’s molecular mechanisms of action are concentration dependent and different than that of other anti-estrogens. PLoS ONE 8:e54613CrossRefPubMedPubMedCentral Hawse JR, Subramaniam M, Cicek M et al (2013) Endoxifen’s molecular mechanisms of action are concentration dependent and different than that of other anti-estrogens. PLoS ONE 8:e54613CrossRefPubMedPubMedCentral
3.
go back to reference Lim YC, Desta Z, Flockhart DA, Skaar TC (2005) Endoxifen (4-hydroxy-N-desmethyl-tamoxifen) has anti-estrogenic effects in breast cancer cells with potency similar to 4-hydroxy-tamoxifen. Cancer Chemother Pharmacol 55:471–478CrossRefPubMed Lim YC, Desta Z, Flockhart DA, Skaar TC (2005) Endoxifen (4-hydroxy-N-desmethyl-tamoxifen) has anti-estrogenic effects in breast cancer cells with potency similar to 4-hydroxy-tamoxifen. Cancer Chemother Pharmacol 55:471–478CrossRefPubMed
4.
go back to reference Murdter TE, Schroth W, Bacchus-Gerybadze L et al (2011) Activity levels of tamoxifen metabolites at the estrogen receptor and the impact of genetic polymorphisms of phase I and II enzymes on their concentration levels in plasma. Clin Pharmacol Ther 89:708–717CrossRefPubMed Murdter TE, Schroth W, Bacchus-Gerybadze L et al (2011) Activity levels of tamoxifen metabolites at the estrogen receptor and the impact of genetic polymorphisms of phase I and II enzymes on their concentration levels in plasma. Clin Pharmacol Ther 89:708–717CrossRefPubMed
5.
go back to reference Baxter SD, Teft WA, Choi YH, Winquist E, Kim RB (2014) Tamoxifen-associated hot flash severity is inversely correlated with endoxifen concentration and CYP3A4*22. Breast Cancer Res Treat 145:419–428CrossRefPubMed Baxter SD, Teft WA, Choi YH, Winquist E, Kim RB (2014) Tamoxifen-associated hot flash severity is inversely correlated with endoxifen concentration and CYP3A4*22. Breast Cancer Res Treat 145:419–428CrossRefPubMed
6.
go back to reference Zembutsu H (2015) Pharmacogenomics toward personalized tamoxifen therapy for breast cancer. Pharmacogenomics 16:287–296CrossRefPubMed Zembutsu H (2015) Pharmacogenomics toward personalized tamoxifen therapy for breast cancer. Pharmacogenomics 16:287–296CrossRefPubMed
8.
go back to reference Binkhorst L, Mathijssen RH, van Herk-Sukel MP et al (2013) Unjustified prescribing of CYP2D6 inhibiting SSRIs in women treated with tamoxifen. Breast Cancer ResTreat 139:923–929CrossRef Binkhorst L, Mathijssen RH, van Herk-Sukel MP et al (2013) Unjustified prescribing of CYP2D6 inhibiting SSRIs in women treated with tamoxifen. Breast Cancer ResTreat 139:923–929CrossRef
9.
go back to reference Kelly CM, Juurlink DN, Gomes T et al (2010) Selective serotonin reuptake inhibitors and breast cancer mortality in women receiving tamoxifen: a population based cohort study. BMJ 340:c693CrossRefPubMedPubMedCentral Kelly CM, Juurlink DN, Gomes T et al (2010) Selective serotonin reuptake inhibitors and breast cancer mortality in women receiving tamoxifen: a population based cohort study. BMJ 340:c693CrossRefPubMedPubMedCentral
10.
go back to reference Madlensky L, Natarajan L, Tchu S et al (2011) Tamoxifen metabolite concentrations, CYP2D6 genotype, and breast cancer outcomes. Clin Pharmacol Ther 89:718–725CrossRefPubMedPubMedCentral Madlensky L, Natarajan L, Tchu S et al (2011) Tamoxifen metabolite concentrations, CYP2D6 genotype, and breast cancer outcomes. Clin Pharmacol Ther 89:718–725CrossRefPubMedPubMedCentral
11.
go back to reference Saladores P, Murdter T, Eccles D et al (2015) Tamoxifen metabolism predicts drug concentrations and outcome in premenopausal patients with early breast cancer. Pharmacogenomics J 15:84–94CrossRefPubMed Saladores P, Murdter T, Eccles D et al (2015) Tamoxifen metabolism predicts drug concentrations and outcome in premenopausal patients with early breast cancer. Pharmacogenomics J 15:84–94CrossRefPubMed
12.
13.
go back to reference Rossmanith WG, Ruebberdt W (2009) What causes hot flushes? The neuroendocrine origin of vasomotor symptoms in the menopause. Gynecol Endocrinol 25:303–314CrossRefPubMed Rossmanith WG, Ruebberdt W (2009) What causes hot flushes? The neuroendocrine origin of vasomotor symptoms in the menopause. Gynecol Endocrinol 25:303–314CrossRefPubMed
14.
go back to reference Del RM, Citi V, Crucitta S et al (2016) Pharmacogenetics of CYP2D6 and tamoxifen therapy: light at the end of the tunnel? Pharmacol Res 107:398–406CrossRef Del RM, Citi V, Crucitta S et al (2016) Pharmacogenetics of CYP2D6 and tamoxifen therapy: light at the end of the tunnel? Pharmacol Res 107:398–406CrossRef
15.
go back to reference Deecher DC, Dorries K (2007) Understanding the pathophysiology of vasomotor symptoms (hot flushes and night sweats) that occur in perimenopause, menopause, and postmenopause life stages. Arch Womens Ment Health 10:247–257CrossRefPubMed Deecher DC, Dorries K (2007) Understanding the pathophysiology of vasomotor symptoms (hot flushes and night sweats) that occur in perimenopause, menopause, and postmenopause life stages. Arch Womens Ment Health 10:247–257CrossRefPubMed
16.
go back to reference Kronenberg F (2010) Menopausal hot flashes: a review of physiology and biosociocultural perspective on methods of assessment. J Nutr 140:1380S–1385SCrossRefPubMed Kronenberg F (2010) Menopausal hot flashes: a review of physiology and biosociocultural perspective on methods of assessment. J Nutr 140:1380S–1385SCrossRefPubMed
17.
go back to reference Lorizio W, Wu AH, Beattie MS et al (2012) Clinical and biomarker predictors of side effects from tamoxifen. Breast Cancer ResTreat 132:1107–1118CrossRef Lorizio W, Wu AH, Beattie MS et al (2012) Clinical and biomarker predictors of side effects from tamoxifen. Breast Cancer ResTreat 132:1107–1118CrossRef
18.
go back to reference Mortimer JE, Flatt SW, Parker BA et al (2008) Tamoxifen, hot flashes and recurrence in breast cancer. Breast Cancer Res Treat 108:421–426CrossRefPubMed Mortimer JE, Flatt SW, Parker BA et al (2008) Tamoxifen, hot flashes and recurrence in breast cancer. Breast Cancer Res Treat 108:421–426CrossRefPubMed
19.
go back to reference Goetz MP, Rae JM, Suman VJ et al (2005) Pharmacogenetics of tamoxifen biotransformation is associated with clinical outcomes of efficacy and hot flashes. J Clin Oncol 23:9312–9318CrossRefPubMed Goetz MP, Rae JM, Suman VJ et al (2005) Pharmacogenetics of tamoxifen biotransformation is associated with clinical outcomes of efficacy and hot flashes. J Clin Oncol 23:9312–9318CrossRefPubMed
20.
go back to reference Henry NL, Rae JM, Li L et al (2009) Association between CYP2D6 genotype and tamoxifen-induced hot flashes in a prospective cohort. Breast Cancer ResTreat 117:571–575CrossRef Henry NL, Rae JM, Li L et al (2009) Association between CYP2D6 genotype and tamoxifen-induced hot flashes in a prospective cohort. Breast Cancer ResTreat 117:571–575CrossRef
21.
go back to reference Sestak I, Kealy R, Nikoloff M et al (2012) Relationships between CYP2D6 phenotype, breast cancer and hot flushes in women at high risk of breast cancer receiving prophylactic tamoxifen: results from the IBIS-I trial. Br J Cancer 107:230–233CrossRefPubMedPubMedCentral Sestak I, Kealy R, Nikoloff M et al (2012) Relationships between CYP2D6 phenotype, breast cancer and hot flushes in women at high risk of breast cancer receiving prophylactic tamoxifen: results from the IBIS-I trial. Br J Cancer 107:230–233CrossRefPubMedPubMedCentral
22.
go back to reference Dezentje VO, Gelderblom H, van Schaik RH et al (2014) CYP2D6 genotype in relation to hot flashes as tamoxifen side effect in a Dutch cohort of the tamoxifen exemestane adjuvant multinational (TEAM) trial. Breast Cancer Res Treat 143:171–179CrossRefPubMed Dezentje VO, Gelderblom H, van Schaik RH et al (2014) CYP2D6 genotype in relation to hot flashes as tamoxifen side effect in a Dutch cohort of the tamoxifen exemestane adjuvant multinational (TEAM) trial. Breast Cancer Res Treat 143:171–179CrossRefPubMed
23.
go back to reference Fox P, Balleine RL, Lee C et al (2016) Dose escalation of tamoxifen in patients with low endoxifen level: evidence for therapeutic drug monitoring-the TADE study. Clin Cancer Res 22:3164–3171CrossRefPubMed Fox P, Balleine RL, Lee C et al (2016) Dose escalation of tamoxifen in patients with low endoxifen level: evidence for therapeutic drug monitoring-the TADE study. Clin Cancer Res 22:3164–3171CrossRefPubMed
24.
go back to reference Jager NG, Koornstra RH, Vincent AD et al (2013) Hot flashes are not predictive for serum concentrations of tamoxifen and its metabolites. BMC Cancer 13:612CrossRefPubMedPubMedCentral Jager NG, Koornstra RH, Vincent AD et al (2013) Hot flashes are not predictive for serum concentrations of tamoxifen and its metabolites. BMC Cancer 13:612CrossRefPubMedPubMedCentral
25.
go back to reference Sloan JA, Loprinzi CL, Novotny PJ, Barton DL, Lavasseur BI, Windschitl H (2001) Methodologic lessons learned from hot flash studies. J Clin Oncol 19:4280–4290CrossRefPubMed Sloan JA, Loprinzi CL, Novotny PJ, Barton DL, Lavasseur BI, Windschitl H (2001) Methodologic lessons learned from hot flash studies. J Clin Oncol 19:4280–4290CrossRefPubMed
26.
go back to reference R Core Team (2016) R. A language and environment for statistical computing, in R Foundation for Statistical Computing. Vienna, Austria. (online source) R Core Team (2016) R. A language and environment for statistical computing, in R Foundation for Statistical Computing. Vienna, Austria. (online source)
27.
go back to reference Gupta P, Sturdee DW, Palin SL et al (2006) Menopausal symptoms in women treated for breast cancer: the prevalence and severity of symptoms and their perceived effects on quality of life. Climacteric 9:49–58CrossRefPubMed Gupta P, Sturdee DW, Palin SL et al (2006) Menopausal symptoms in women treated for breast cancer: the prevalence and severity of symptoms and their perceived effects on quality of life. Climacteric 9:49–58CrossRefPubMed
28.
go back to reference Irvin WJ Jr, Walko CM, Weck KE et al (2011) Genotype-guided tamoxifen dosing increases active metabolite exposure in women with reduced CYP2D6 metabolism: a multicenter study. J Clin Oncol 29:3232–3239CrossRefPubMedPubMedCentral Irvin WJ Jr, Walko CM, Weck KE et al (2011) Genotype-guided tamoxifen dosing increases active metabolite exposure in women with reduced CYP2D6 metabolism: a multicenter study. J Clin Oncol 29:3232–3239CrossRefPubMedPubMedCentral
29.
go back to reference Mortimer J, Behrendt CE (2013) Severe menopausal symptoms are widespread among survivors of breast cancer treatment regardless of time since diagnosis. J Palliat Med 16:1130–1134CrossRefPubMed Mortimer J, Behrendt CE (2013) Severe menopausal symptoms are widespread among survivors of breast cancer treatment regardless of time since diagnosis. J Palliat Med 16:1130–1134CrossRefPubMed
Metadata
Title
CYP2D6 genotype and endoxifen plasma concentration do not predict hot flash severity during tamoxifen therapy
Authors
Laura E. Jansen
Wendy A. Teft
Rhiannon V. Rose
Daniel J. Lizotte
Richard B. Kim
Publication date
01-10-2018
Publisher
Springer US
Published in
Breast Cancer Research and Treatment / Issue 3/2018
Print ISSN: 0167-6806
Electronic ISSN: 1573-7217
DOI
https://doi.org/10.1007/s10549-018-4876-x

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