Literature DB >> 30456916

Statin use and survival in patients with gastric cancer in two independent population-based cohorts.

Andrew D Spence1, John Busby1, Carmel M Hughes2, Brian T Johnston3, Helen G Coleman1,4, Chris R Cardwell1.   

Abstract

PURPOSE: Preclinical studies show statins inhibit pathways involved in gastric cancer progression, with observational studies demonstrating reduced gastric cancer risk in statin users. However, few studies have investigated statin use and survival in gastric cancer. We investigated statin use and survival in two large population-based gastric cancer cohorts.
METHODS: Patients diagnosed with gastric cancer from 1998 to 2012 were identified from English and Scottish cancer registries. Statin prescriptions were identified from linkages to the UK Clinical Practice Research Datalink in England and the Prescribing Information System in Scotland, and deaths identified from national mortality records. Time-dependent Cox regression models were used to calculate hazard ratios (HR) and 95% confidence intervals (CIs) for cancer-specific mortality by statin use in multivariate analysis. Meta-analysis techniques pooled results across the cohorts.
RESULTS: The combined cohorts contained 3833 patients with gastric cancer and 2392 cancer-specific deaths. Statin use after diagnosis was associated with reduced cancer-specific mortality (adjusted HR 0.83; 95% CI, 0.74-0.92). HRs for less than 1 year and over 1 year of statin use were similar (adjusted HR 0.83; 95% CI, 0.73-0.94 and adjusted HR 0.83; 95% CI, 0.64-1.01, respectively). Statin use prior to diagnosis was also associated with reduced cancer-specific mortality (adjusted HR 0.91; 95% CI, 0.84-0.98).
CONCLUSIONS: In two independent UK cohorts, there was some evidence that statin use was associated with reduced cancer-specific mortality. However, these associations were weak in magnitude and did not follow a clear dose response, and we cannot rule out confounding by stage.
© 2018 John Wiley & Sons, Ltd.

Entities:  

Keywords:  cancer biology; epidemiology; gastric cancer; pharmacoepidemiology; statins; stomach; survival

Mesh:

Substances:

Year:  2018        PMID: 30456916     DOI: 10.1002/pds.4688

Source DB:  PubMed          Journal:  Pharmacoepidemiol Drug Saf        ISSN: 1053-8569            Impact factor:   2.890


  6 in total

Review 1.  Statins Are Associated with Improved Survival of Patients with Gastric Cancer: A Systematic Review and Meta-Analysis.

Authors:  Mingjie Yuan; Shuyi Han; Yanfei Jia; Jiankai Feng; Duanrui Liu; Zhenguo Su; Xiangdong Liu
Journal:  Int J Clin Pract       Date:  2022-05-17       Impact factor: 3.149

Review 2.  Improving prescribing through big data approaches-Ten years of the Scottish Prescribing Information System.

Authors:  Marion Bennie; William Malcolm; Stuart McTaggart; Tanja Mueller
Journal:  Br J Clin Pharmacol       Date:  2020-01-17       Impact factor: 3.716

3.  Aspirin use in relation to long-term survival after gastrectomy for gastric adenocarcinoma.

Authors:  Dag Holmberg; Joonas H Kauppila; Fredrik Mattsson; Johannes Asplund; Wilhelm Leijonmarck; Shao-Hua Xie; Jesper Lagergren
Journal:  Gastric Cancer       Date:  2022-02-15       Impact factor: 7.701

4.  Statin Use Improves Overall Survival of Patients with Gastric Cancer after Surgery and Adjuvant Chemotherapy in Taiwan: A Nationwide Matched Cohort Study.

Authors:  Pei-Rung Yang; Ying-Ying Tsai; Ko-Jung Chen; Yao-Hsu Yang; Wei-Tai Shih
Journal:  Cancers (Basel)       Date:  2020-07-25       Impact factor: 6.639

5.  Association between Statin Use and Gastric Cancer: A Nested Case-Control Study Using a National Health Screening Cohort in Korea.

Authors:  Mi Jung Kwon; Ho Suk Kang; Joo-Hee Kim; Ji Hee Kim; Se Hoon Kim; Nan Young Kim; Eun Sook Nam; Kyueng-Whan Min; Hyo Geun Choi
Journal:  Pharmaceuticals (Basel)       Date:  2021-12-08

Review 6.  Statin as a therapeutic agent in gastroenterological cancer.

Authors:  Norio Uemura; Hiromitsu Hayashi; Hideo Baba
Journal:  World J Gastrointest Oncol       Date:  2022-01-15
  6 in total

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