The deleterious association between proton pump inhibitors and prostate cancer-specific mortality – a population-based cohort study
Autor: | Miran Kenk, Thenappan Chandrasekar, Christopher J.D. Wallis, Shabbir M.H. Alibhai, Hanan Goldberg, Girish S. Kulkarni, Linda Z. Penn, Olli Saarela, Zachary Klaassen, Alejandro Berlin, Faizan K. Mohsin, Refik Saskin, Neil Fleshner |
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Rok vydání: | 2020 |
Předmět: |
Oncology
Cancer Research medicine.medical_specialty Prostate biopsy medicine.diagnostic_test Proportional hazards model business.industry Urology 030232 urology & nephrology Cancer medicine.disease Comorbidity Androgen deprivation therapy 03 medical and health sciences Prostate cancer 0302 clinical medicine 030220 oncology & carcinogenesis Internal medicine Cohort medicine business Pantoprazole medicine.drug |
Zdroj: | Prostate Cancer and Prostatic Diseases. 23:622-629 |
ISSN: | 1476-5608 1365-7852 |
DOI: | 10.1038/s41391-020-0248-9 |
Popis: | Proton pump inhibitors (PPIs) are commonly prescribed medications that have been shown to have contradicting effects on cancer. We aimed to investigate the effect of pantoprazole and other PPIs on prostate cancer (PCa) specific mortality (PCSM), use of androgen deprivation therapy (ADT), and PCa diagnosis using a large Canadian population-based cohort. We identified 21,512 men aged ≥ 66, with a history of a single negative prostate biopsy and no previous use of any of the analyzed medications between 1994 and 2016. Multivariable Cox regression models with time-dependent covariates were used to assess the associations of PPIs with PCa outcomes. All models included other medications with a putative chemopreventative effect on PCa-outcomes, and were adjusted for age, rurality, comorbidity, and study inclusion year. Over a mean follow-up of 8.06 years (SD 5.44 years), 10,999 patients (51.1%) used a PPI, 5187 patients (24.1%) had PCa, 2043 patients (9.5%) were treated with ADT, and 805 patients (3.7%) died from PCa. For every 6 months of cumulative use, pantoprazole was associated with a 3.0% (95% CI 0.3–6.0%) increased rate of ADT use, while any use of other PPIs was associated with a 39.0% (95% CI 18.0–64.0%) increased risk of PCSM. No association was found with PCa diagnosis. Upon validation of the potentially negative association of PPIs with PCa, PPI use may need to be reassessed in PCa patients. |
Databáze: | OpenAIRE |
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