User profiles for Werner Schroth
Werner SchrothInstitute of Clinical Pharmacology Stuttgart Verified email at ikp-stuttgart.de Cited by 4860 |
A new molecular predictor of distant recurrence in ER-positive, HER2-negative breast cancer adds independent information to conventional clinical risk factors
Purpose: According to current guidelines, molecular tests predicting the outcome of breast
cancer patients can be used to assist in making treatment decisions after consideration of …
cancer patients can be used to assist in making treatment decisions after consideration of …
Association between CYP2D6 polymorphisms and outcomes among women with early stage breast cancer treated with tamoxifen
Context The growth inhibitory effect of tamoxifen, which is used for the treatment of hormone
receptor–positive breast cancer, is mediated by its metabolites, 4-hydroxytamoxifen and …
receptor–positive breast cancer, is mediated by its metabolites, 4-hydroxytamoxifen and …
[PDF][PDF] Breast cancer treatment outcome with adjuvant tamoxifen relative to patient CYP2D6 and CYP2C19 genotypes
W Schroth, L Antoniadou, P Fritz… - Journal of Clinical …, 2007 - researchgate.net
Purpose The clinical outcome of tamoxifen-treated breast cancer patients may be influenced
by the activity of cytochrome P450 enzymes that catalyze the formation of antiestrogenic …
by the activity of cytochrome P450 enzymes that catalyze the formation of antiestrogenic …
[HTML][HTML] Speciation and phylogeography in the cosmopolitan marine moon jelly, Aurelia sp
Background The cosmopolitan moon jelly Aurelia is characterized by high degrees of
morphological and ecological plasticity, and subsequently by an unclear taxonomic status. The …
morphological and ecological plasticity, and subsequently by an unclear taxonomic status. The …
CYP2D6 Genotype and Adjuvant Tamoxifen: Meta‐Analysis of Heterogeneous Study Populations
The International Tamoxifen Pharmacogenomics Consortium was established to address
the controversy regarding cytochrome P450 2D6 (CYP2D6) status and clinical outcomes in …
the controversy regarding cytochrome P450 2D6 (CYP2D6) status and clinical outcomes in …
[HTML][HTML] Tamoxifen use in postmenopausal breast cancer: CYP2D6 matters
The question of whether genetic polymorphisms of CYP2D6 can affect treatment outcome in
patients with early postmenopausal breast cancer has been a matter of debate. With the …
patients with early postmenopausal breast cancer has been a matter of debate. With the …
[HTML][HTML] Increased expression of miR-126 and miR-10a predict prolonged relapse-free time of primary oestrogen receptor-positive breast cancer following tamoxifen …
…, S Winter, P Fritz, WY Lo, W Schroth… - European journal of …, 2013 - Elsevier
Background Adjuvant tamoxifen is a valid treatment option for women with oestrogen receptor
(ER)-positive breast cancer. However, up to 40% of patients experience distant or local …
(ER)-positive breast cancer. However, up to 40% of patients experience distant or local …
CYP2D6 Polymorphisms as Predictors of Outcome in Breast Cancer Patients Treated with Tamoxifen: Expanded Polymorphism Coverage Improves Risk Stratification
W Schroth, U Hamann, PA Fasching, S Dauser… - Clinical Cancer …, 2010 - AACR
Purpose: This study aimed to validate matrix-assisted laser desorption/ionization–time-of-flight
mass spectrometry (MALDI-TOF MS)/Taqman copy number assay (CNA) CYP2D6 …
mass spectrometry (MALDI-TOF MS)/Taqman copy number assay (CNA) CYP2D6 …
[HTML][HTML] Improved prediction of endoxifen metabolism by CYP2D6 genotype in breast cancer patients treated with tamoxifen
Purpose: Prediction of impaired tamoxifen (TAM) to endoxifen metabolism may be relevant
to improve breast cancer treatment, eg, via TAM dose increase. The polymorphic cytochrome …
to improve breast cancer treatment, eg, via TAM dose increase. The polymorphic cytochrome …
[HTML][HTML] Cancer-Associated Intermediate Conductance Ca2+-Activated K+ Channel KCa3.1
…, D Gross, P Ruth, WY Lo, R Hoppe, W Schroth… - Cancers, 2019 - mdpi.com
Several tumor entities have been reported to overexpress K Ca 3.1 potassium channels due
to epigenetic, transcriptional, or post-translational modifications. By modulating membrane …
to epigenetic, transcriptional, or post-translational modifications. By modulating membrane …