Bibliographic Details
Title: |
Association of CYP2D6 genotype and tamoxifen metabolites with breast cancer recurrence in a low-dose trial |
Authors: |
Andrea DeCensi, Harriet Johansson, Thomas Helland, Matteo Puntoni, Debora Macis, Valentina Aristarco, Silvia Caviglia, Tania Buttiron Webber, Irene Maria Briata, Mauro D’Amico, Davide Serrano, Aliana Guerrieri-Gonzaga, Ersilia Bifulco, Steinar Hustad, Håvard Søiland, Luca Boni, Bernardo Bonanni, Gunnar Mellgren |
Source: |
npj Breast Cancer, Vol 7, Iss 1, Pp 1-5 (2021) |
Publisher Information: |
Nature Portfolio, 2021. |
Publication Year: |
2021 |
Collection: |
LCC:Neoplasms. Tumors. Oncology. Including cancer and carcinogens |
Subject Terms: |
Neoplasms. Tumors. Oncology. Including cancer and carcinogens, RC254-282 |
More Details: |
Abstract Low-dose tamoxifen halves recurrence in non-invasive breast cancer without significant adverse events. Some adjuvant trials with tamoxifen 20 mg/day had shown an association between low endoxifen levels (9–16 nM) and recurrence, but no association with CYP2D6 was shown in the NSABP P1 and P2 prevention trials. We studied the association of CYP2D6 genotype and tamoxifen metabolites with tumor biomarkers and recurrence in a randomized phase III trial of low-dose tamoxifen. Median (IQR) endoxifen levels at year 1 were 8.4 (5.3–11.4) in patients who recurred vs 7.5 (5.1–10.2) in those who did not recur (p = 0.60). Tamoxifen and metabolites significantly decreased C-reactive protein (CRP, p |
Document Type: |
article |
File Description: |
electronic resource |
Language: |
English |
ISSN: |
2374-4677 |
Relation: |
https://doaj.org/toc/2374-4677 |
DOI: |
10.1038/s41523-021-00236-6 |
Access URL: |
https://doaj.org/article/970405befd6e48368a4c4d7033f964aa |
Accession Number: |
edsdoj.970405befd6e48368a4c4d7033f964aa |
Database: |
Directory of Open Access Journals |