Impact of systemic adjuvant therapy and CYP2D6 activity on mammographic density in a cohort of tamoxifen-treated breast cancer patients.
Adjuvant treatment
Breast cancer
CYP2D6
Chemotherapy
Mammographic density
Tamoxifen
Journal
Breast cancer research and treatment
ISSN: 1573-7217
Titre abrégé: Breast Cancer Res Treat
Pays: Netherlands
ID NLM: 8111104
Informations de publication
Date de publication:
Dec 2021
Dec 2021
Historique:
received:
20
05
2021
accepted:
06
09
2021
pubmed:
28
9
2021
medline:
3
11
2021
entrez:
27
9
2021
Statut:
ppublish
Résumé
Change in mammographic density has been suggested to be a proxy of tamoxifen response. We investigated the effect of additional adjuvant systemic therapy and CYP2D6 activity on MD change in a cohort of tamoxifen-treated pre- and postmenopausal breast cancer patients. Swedish breast cancer patients (n = 699) operated 2006-2014, genotyped for CYP2D6, having at least three months postoperative tamoxifen treatment, a baseline, and at least one follow-up digital mammogram were included in the study. Other systemic adjuvant treatment included chemotherapy, goserelin, and aromatase inhibitors. Change in MD, dense area, was assessed using the automated STRATUS method. Patients were stratified on baseline characteristics, treatments, and CYP2D6 activity (poor, intermediate, extensive, and ultrarapid). Relative density change was calculated at year 1, 2, and 5 during follow-up in relation to treatments and CYP2D6 activity. Mean relative DA decreased under the follow-up period, with a more pronounced MD reduction in premenopausal patients. No significant effect of chemotherapy, aromatase inhibitors, goserelin, or CYP2D6 activity on DA change was found. DA did not revert to baseline levels after tamoxifen discontinuation. Our results indicate that other systemic adjuvant therapy does not further reduce MD in tamoxifen-treated breast cancer patients. We could not confirm the previously suggested association between CYP2D6 activity and MD reduction in a clinical setting with multimodality adjuvant treatment. No rebound effect on MD decline after tamoxifen discontinuation was evident.
Identifiants
pubmed: 34570302
doi: 10.1007/s10549-021-06386-2
pii: 10.1007/s10549-021-06386-2
pmc: PMC8558195
doi:
Substances chimiques
Antineoplastic Agents, Hormonal
0
Tamoxifen
094ZI81Y45
Cytochrome P-450 CYP2D6
EC 1.14.14.1
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
451-462Subventions
Organisme : Stockholm County Council
ID : ALF20180419
Organisme : Stockholms Läns Landsting
ID : ALF20190536
Organisme : the Swedish Cancer Society
ID : 19 0292 PJ 01 H
Organisme : the Swedish Cancer Society
ID : 19 0189 US01 H
Organisme : The Research Funds at Radiumhemmet
ID : 164003
Organisme : Stockholm County Council
ID : ALF2017-1341
Organisme : FOU
ID : Karolinska University Hospital account number 907515
Informations de copyright
© 2021. The Author(s).
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