Statin therapy is associated with improved survival in patients with non-serous-papillary epithelial ovarian cancer: a retrospective cohort analysis
Autor: | S. Diane Yamada, Lacey M. Litchfield, Mohammed Habis, Michael J. Bradaric, Nadia Ismail, Ernst Lengyel, Kristen Wroblewski, Iris L. Romero |
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Jazyk: | angličtina |
Rok vydání: | 2014 |
Předmět: |
Oncology
endocrine system diseases Epidemiology Cancer Treatment lcsh:Medicine Pathology and Laboratory Medicine Cohort Studies Hyperlipidemia Basic Cancer Research Drug Discovery Medicine and Health Sciences lcsh:Science Ovarian Neoplasms Likelihood Functions Multidisciplinary Cancer Drug Discovery Pharmaceutics Cancer Risk Factors Confounding Endocrine Therapy 3. Good health Ovarian Cancer Nutritional Correlates of Cancer Cohort Cancer Therapy Female Lovastatin Cancer Epidemiology medicine.drug Cohort study Research Article medicine.medical_specialty Drug Research and Development Hyperlipidemias Disease-Free Survival Signs and Symptoms Drug Therapy Diabetes mellitus Internal medicine medicine Humans cardiovascular diseases Cell Proliferation Retrospective Studies Pharmacology business.industry lcsh:R Cancers and Neoplasms nutritional and metabolic diseases Retrospective cohort study medicine.disease Surgery lcsh:Q Hydroxymethylglutaryl-CoA Reductase Inhibitors business Ovarian cancer Gynecological Tumors |
Zdroj: | PLoS ONE, Vol 9, Iss 8, p e104521 (2014) PLoS ONE |
ISSN: | 1932-6203 |
Popis: | Aim To determine whether statin use is associated with improved epithelial ovarian cancer (OvCa) survival. Methods This is a single-institution retrospective cohort review of patients treated for OvCa between 1992 and 2013. Inclusion criteria were International Federation of Gynecology and Obstetrics (FIGO) stage I–IV OvCa. The primary exposures analyzed were hyperlipidemia and statin use. The primary outcomes were progression-free survival (PFS) and disease-specific survival (DSS). Results 442 patients met inclusion criteria. The cohort was divided into three groups: patients with hyperlipidemia who used statins (n = 68), patients with hyperlipidemia who did not use statins (n = 28), and patients without hyperlipidemia (n = 346). OvCa outcomes were evaluated. When we analyzed the entire cohort, we found no significant differences in PFS or DSS among the groups. The median PFS for hyperlipidemics using statins, hyperlipidemics not using statins, and non-hyperlipidemics was 21.7, 13.6, and 14.7 months, respectively (p = 0.69). Median DSS for hyperlipidemics using statins, hyperlipidemics not using statins, and non-hyperlipidemics was 44.2, 75.7, and 41.5 months, respectively (p = 0.43). These findings did not change after controlling for confounders. However, a secondary analysis revealed that, among patients with non-serous-papillary subtypes of OvCa, statin use was associated with a decrease in hazards of both disease recurrence (adjusted HR = 0.23, p = 0.02) and disease-specific death (adjusted HR = 0.23, p = 0.04). To augment the findings in the retrospective cohort, the histology-specific effects of statins were also evaluated in vitro using proliferation assays. Here, statin treatment of cell lines resulted in a variable level of cytotoxicity. Conclusion Statin use among patients with non-serous-papillary OvCa was associated with improvement in both PFS and DSS. |
Databáze: | OpenAIRE |
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