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Research article:

Exposure to sodium channel-inhibiting drugs and cancer survival: protocol for a cohort study using the QResearch primary care database

Reference:

Caroline Fairhurst, Ian Watt, Fabiola Martin, Martin Bland, and William J. Brackenbury(2014) Exposure to sodium channel-inhibiting drugs and cancer survival: protocol for a cohort study using the QResearch primary care database. BMJ Open, doi:

Link to fulltext article
Abstract
Introduction: Metastasis from solid tumours is associated with significant morbidity and mortality, and is the leading cause of cancer-related deaths. Voltage-gated sodium channels (VGSCs) are drug targets for the treatment of epilepsy. VGSCs are also present in cancer cells, where they regulate metastatic cell behaviours, including cellular movement and invasion. Treating cancer cells with the VGSC-inhibiting anticonvulsant phenytoin reduces cellular invasion and migration. Together, these suggest that VGSCs may be useful targets for inhibiting metastasis. The purpose of this study is to test the hypothesis that use of VGSC-inhibiting drugs will reduce metastasis, and therefore increase survival time in cancer patients. Methods and analysis: A cohort study based on primary care data from the QResearch database will include patients with one of three common tumours: breast, bowel, and prostate. The primary outcome will be overall survival from date of cancer diagnosis. Cox proportional hazards regression will be used to compare the survival of cancer patients taking VGSC-inhibiting drugs (including anticonvulsants and Class I antiarrhythmic agents) with cancer patients not exposed to these drugs, adjusting for age and sex. Exposure to VGSC-inhibiting drugs will be defined as having at least one prescription for these drugs prior to cancer diagnosis. High and low exposure groups will be identified based on length of use. A number of sensitivity and secondary analyses will be conducted. Ethics and dissemination: The protocol has been independently peer-reviewed and approved by the QResearch Scientific Board. The project has also been approved by the University of York Ethical Review Process. The results will be presented at international conferences and published in an open access peer-reviewed journal, in accordance with the STROBE criteria.
Author for correspondence
William J. Brackenbury
Email for correspondence
william.brackenbury@york.ac.uk

Code list: res17: Prostate cancer

18 codes in list

Code Coding system Description Entity type List name
14270 Read H/O: prostate cancer diagnostic res17: Prostate cancer
1J08 Read Suspected prostate cancer diagnostic res17: Prostate cancer
4M0 Read Gleason grading of prostate cancer diagnostic res17: Prostate cancer
4M00 Read Gleason prostate grade 2-4 (low) diagnostic res17: Prostate cancer
4M01 Read Gleason prostate grade 5-7 (medium) diagnostic res17: Prostate cancer
4M02 Read Gleason prostate grade 8-10 (high) diagnostic res17: Prostate cancer
B46 Read Malignant neoplasm of prostate diagnostic res17: Prostate cancer
B58y5 Read Secondary malignant neoplasm of prostate diagnostic res17: Prostate cancer
B7C20 Read Adenoma of prostate diagnostic res17: Prostate cancer
B834 Read Carcinoma in situ of prostate diagnostic res17: Prostate cancer
B8340 Read High grade prostatic intraepithelial neoplasia diagnostic res17: Prostate cancer
B8341 Read Prostatic intraepithelial neoplasia diagnostic res17: Prostate cancer
B915 Read Neoplasm of uncertain behaviour of prostate diagnostic res17: Prostate cancer
EMISNQPR140 Read Prostatic intraepithelial neoplasia diagnostic res17: Prostate cancer
HNG0200 Read [RFC] Cancer of the prostate diagnostic res17: Prostate cancer
K223 Read Dysplasia of prostate diagnostic res17: Prostate cancer
PCSDT1PR16 Read Prostate carcinoma diagnostic res17: Prostate cancer
ZV104-5 Read [V]Personal history of malignant neoplasm of prostate diagnostic res17: Prostate cancer

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