Raadpleeg ook de literatuurlijsten van niet-toxische middelen en behandelingen bij individuele vormen van kanker en chemo en bestraling en operatie en stamceltransplantaties
4 oktober 2023: dagelijks aspirinegebruik wordt afgeraden op basis van deze meta-analyse uit 2021 want blijkt toch niet echt vormen van kanker te kunnen voorkomen:
Abstract onderaan dit artikel
14 november 2018: Bron: BMC Cancer. 2018; 18: 288. Published online 2018 Mar 13.
Al heel lang wordt onderzocht wat aspirinegebruik doet bij kanker. Werkt het preventief? Voorkomt het een recidief? Wat zijn de bijwerkingen en gevaren van langdurig aspirinegebruik?
Hier hebben we een aantal studiepublicaties bij elkaar gebracht in een overzicht, zie ook bij darmkanker - preventie in gerelateerde artikelen. Of in gerelateerde artikelen bij dit artikel (tekst gaat verder onder beeld)
Maar raadpleeg ook deze reviewstudie / meta analyse:
Associations between aspirin use and the risk of cancers: a meta-analysis of observational studies
De belangrijkste resultaten uit 218 artikelen uit de periode tussen 1985 en 2016 zijn samengevat in grafieken uitgesplitst naar vorm van kanker.
Klik op de grafieken voor de resultaten en studies per vorm van kanker: , , , , , , , , , , , , , , , , , , , en .
Deze studie omvatte in totaal 161 cohortstudies en 148 case-control studies. Onder hen zijn 135 studies uitgevoerd in Noord-Amerika, 12 in Azië, 61 in Europa, 8 in Oceanië en 2 in meerdere landen. Over het algemeen was de samengevatte RR 0.89 (95% CI: 0.87-0.91), wat wijst op een verminderd risico op kanker geassocieerd met het gebruik van aspirine. De gecombineerde RR's waren 0,82 (95% CI: 0,79-0,85) voor de case-control studies en 0,94 (95% CI: 0,92-0,97) voor de cohortstudies.
Samenvattend lijkt langdurig aspirinegebruik dus verschillende vormen van kanker te kunnen voorkomen.
Genoemd worden maagkanker, darmkanker, slokdarmkanker, borstkanker, alvleesklierkanker, eierstokkanker, endometriosekanker (buikvlieskanker), prostaatkanker en neuro endocriene tumoren in de spijsverteringskanalen
maar er wordt ook gewaarschuwd voor de gevaren en bijwerkingen. O.a. is een van de gevaren dat inwendige bloedingen door langdurig aspirinegebruik kunnen ontstaan.
Hier de originele conclusie van deze meta-analyse met onderaan artikel het abstract en referentielijst. .
Evidence from observational studies indicates that utilization of aspirin is associated with reduced risk of gastric, colorectal, esophageal, pancreatic, ovarian, endometrial, breast, and prostate cancers, in addition to small intestine neuroendocrine tumors. A stronger protective effect was observed in the North American populations and patients who used aspirin for at least 5 years. It is important to address immortal time bias not only to ensure the integrity of the meta-analysis, but also to ensure the integrity of pharmacoepidemiological studies. Moreover, given the confidence limits of the evaluated studies, adequately powered mechanistic studies should help elucidate the mechanisms underlying this correlation.
Hier het abstract plus referentielijst:
These findings suggest that aspirin use is associated with a reduced risk of gastric, esophageal, colorectal, pancreatic, ovarian, endometrial, breast, and prostate cancers, and small intestine neuroendocrine tumors.
Associations between aspirin use and the risk of cancers: a meta-analysis of observational studies
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Abstract
Background
Epidemiological studies have clarified the potential associations between regular aspirin use and cancers. However, it remains controversial on whether aspirin use decreases the risk of cancers risks. Therefore, we conducted an updated meta-analysis to assess the associations between aspirin use and cancers.
Methods
The PubMed, Embase, and Web of Science databases were systematically searched up to March 2017 to identify relevant studies. Relative risks (RRs) with 95% confidence intervals (CIs) were used to assess the strength of associations.
Results
A total of 218 studies with 309 reports were eligible for this meta-analysis. Aspirin use was associated with a significant decrease in the risk of overall cancer (RR = 0.89, 95% CI: 0.87–0.91), and gastric (RR = 0.75, 95% CI: 0.65–0.86), esophageal (RR = 0.75, 95% CI: 0.62–0.89), colorectal (RR = 0.79, 95% CI: 0.74–0.85), pancreatic (RR = 0.80, 95% CI: 0.68–0.93), ovarian (RR = 0.89, 95% CI: 0.83–0.95), endometrial (RR = 0.92, 95% CI: 0.85–0.99), breast (RR = 0.92, 95% CI: 0.88–0.96), and prostate (RR = 0.94, 95% CI: 0.90–0.99) cancers, as well as small intestine neuroendocrine tumors (RR = 0.17, 95% CI: 0.05–0.58).
Conclusions
These findings suggest that aspirin use is associated with a reduced risk of gastric, esophageal, colorectal, pancreatic, ovarian, endometrial, breast, and prostate cancers, and small intestine neuroendocrine tumors.
Electronic supplementary material
The online version of this article (10.1186/s12885-018-4156-5) contains supplementary material, which is available to authorized users.
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Articles from BMC Cancer are provided here courtesy of BioMed Central
High frequency or high dose use of aspirin should be prescribed with caution because of their associations with increased lung and prostate cancer risk, respectively.
, 1 , † , 1 , † , 1 , 1 , 1 , 1 , 1 , * , ‡ and 1 , 2 , * , ‡
Abstract
Background
Whether aspirin use can decrease or increase cancer risk remains controversial. In this study, a meta-analysis of cohort studies and randomized controlled trials (RCTs) were conducted to evaluate the effect of aspirin use on common cancer risk.
Method
Medline and Embase databases were searched to identify relevant studies. Meta-analyses of cohort studies and RCTs were performed to assess the effect of aspirin use on the risk of colorectal, gastric, breast, prostate and lung cancer. Cochran Q test and the I square metric were calculated to detect potential heterogeneity among studies. Subgroup meta-analyses according to exposure categories (frequency and duration) and timing of aspirin use (whether aspirin was used before and after cancer diagnosis) were also performed. A dose-response analysis was carried out to evaluate and quantify the association between aspirin dose and cancer risk.
Results
A total of 88 cohort studies and seven RCTs were included in the final analysis. Meta-analyses of cohort studies revealed that regular aspirin use reduced the risk of colorectal cancer (CRC) (RR=0.85, 95%CI: 0.78-0.92), gastric cancer (RR=0.67, 95%CI: 0.52-0.87), breast cancer (RR=0.93, 95%CI: 0.87-0.99) and prostate cancer (RR=0.92, 95%CI: 0.86-0.98), but showed no association with lung cancer risk. Additionally, meta-analyses of RCTs showed that aspirin use had a protective effect on CRC risk (OR=0.74, 95%CI: 0.56-0.97). When combining evidence from meta-analyses of cohorts and RCTs, consistent evidence was found for the protective effect of aspirin use on CRC risk. Subgroup analysis showed that high frequency aspirin use was associated with increased lung cancer risk (RR=1.05, 95%CI: 1.01-1.09). Dose-response analysis revealed that high-dose aspirin use may increase prostate cancer risk.
Conclusions
This study provides evidence for low-dose aspirin use for the prevention of CRC, but not other common cancers. High frequency or high dose use of aspirin should be prescribed with caution because of their associations with increased lung and prostate cancer risk, respectively. Further studies are warranted to validate these findings and to find the minimum effective dose required for cancer prevention.
Data Availability Statement
The original contributions presented in the study are included in the article/ Supplementary Material . Further inquiries can be directed to the corresponding authors.
Author Contributions
LW and RZ: literature review. LW, LY, and RZ: data extraction. LW, JX, XZ, and XiL: statistical analysis. LW: manuscript preparation. XuL and PS: study conception, design, manuscript review and edit. All authors contributed to the article and approved the submitted version.
Conflict of Interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Acknowledgments
We are very grateful to all teachers and students involved in this study for their contributions and helpful comment.
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