Genetic variants and social benefit receipt in premenopausal women with breast cancer treated with docetaxel: a Danish population-based cohort study
- Julie A Schmidt 1, Cathrine F Hjorth 2, Dóra K Farkas 2, Per Damkier 3,4, Søren Feddersen 4,5, Stephen Hamilton-Dutoit 6, Bent Ejlertsen 7,8, Timothy L Lash 2,9, Thomas P Ahern 10, Deirdre Cronin-Fenton 2
- 1Department of Clinical Epidemiology, Department of Clinical Medicine, Aarhus University and Aarhus University Hospital, Olof Palmes Allé 43-45, 8200, Aarhus N, Denmark. js@clin.au.dk.
- 2Department of Clinical Epidemiology, Department of Clinical Medicine, Aarhus University and Aarhus University Hospital, Olof Palmes Allé 43-45, 8200, Aarhus N, Denmark.
- 3Department of Clinical Pharmacology, Odense University Hospital, Odense, Denmark.
- 4Department of Clinical Research, University of Southern Denmark, Odense, Denmark.
- 5Department of Clinical Biochemistry, Odense University Hospital, Odense, Denmark.
- 6Department of Clinical Medicine and Department of Pathology, Aarhus University Hospital, Aarhus, Denmark.
- 7Danish Breast Cancer Group, Department of Oncology, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.
- 8Department of Clinical Medicine, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
- 9Department of Epidemiology, Rollins School of Public Health, Emory University, Atlanta, GA, USA.
- 10Department of Surgery, The Robert Larner, M.D. College of Medicine, The University of Vermont, Burlington, VT, USA.
- 0Department of Clinical Epidemiology, Department of Clinical Medicine, Aarhus University and Aarhus University Hospital, Olof Palmes Allé 43-45, 8200, Aarhus N, Denmark. js@clin.au.dk.
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View abstract on PubMed
Summary
This summary is machine-generated.This study found no significant link between specific genetic variations (SNPs) and the need for social benefits in breast cancer survivors after taxane chemotherapy. The selected genetic markers did not clinically impact benefit receipt in this patient group.
Area Of Science
- Oncology
- Pharmacogenomics
- Social Sciences
Background
- Taxane-based chemotherapy for breast cancer can lead to long-lasting side effects, potentially increasing patients' need for social benefits.
- Single nucleotide polymorphisms (SNPs) may influence chemotherapy side effects and subsequent social benefit utilization.
Purpose Of The Study
- To investigate the association between specific SNPs (related to taxane metabolism, transport, toxicity, or DNA repair) and the receipt of social benefits in breast cancer patients.
- To determine if genetic variations impact the need for health-related or labor market-related benefits post-chemotherapy.
Main Methods
- Study included 2430 premenopausal women with stage I-III breast cancer treated with docetaxel-based chemotherapy.
- Genotyped 21 SNPs from tumor samples and analyzed nationwide registry data on social benefit payments from 1 year pre-diagnosis to 5 years post-diagnosis.
- Used negative binomial regression to calculate rate ratios (RRs) comparing benefit receipt in variant carriers versus non-carriers.
Main Results
- Approximately 12% of women received health-related benefits pre-diagnosis, 80% at diagnosis, and ~24% 2-5 years post-diagnosis.
- Labor market-related benefits were received by 3-6% of patients.
- All calculated rate ratios (RRs) for the association between SNPs and social benefit receipt were near-null and imprecise.
Conclusions
- The investigated single nucleotide polymorphisms (SNPs) showed no clinically significant impact on social benefit receipt among premenopausal breast cancer survivors undergoing docetaxel treatment.
- These genetic markers do not appear to be reliable predictors of social benefit needs in this population.
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