Cancer Risk
Study register · detail Bevölkerungsbasierte Fall-Kontroll-Studie · Cancer Risk · 2004

Cannabis use and risk of oral squamous cell carcinoma.

No benefit demonstrated GRADE Low 130 citations
Samplen = 1.022 Pat.
Duration1985 to 1995
ControlPopulation-based controls without OSCC…
EndpointOSCC risk
Blindingn.a.
DesignBevölkerungsbasierte Fall-Kontroll-Studie
Key finding

Cannabis use was not associated with an increased risk of oral squamous cell carcinoma in this population-based study.

Summary

Population-based case-control study (n=407 OSCC cases + n=615 controls), cannabis use and risk of oral squamous cell carcinoma: adjusted OR=0,9 (95% CI 0,6–1,3), no increased risk. No trend with increasing duration of use, frequency, or time since first use. No subgroup effect (age, smoking, alcohol, genetic polymorphisms).

P
PopulationAdults (18–65 years) with newly diagnosed oral squamous cell carcinoma (OSCC) and population-based controls, n=1022 (407 cases, 615 controls)
I
InterventionLifetime cannabis use history (ever vs. never, duration, frequency, timing)
C
ControlPopulation-based controls without OSCC diagnosis
O
OutcomeNo increased OSCC risk in cannabis users (adjusted OR 0,9; 95% CI 0,6–1,3); no dose-response trends for duration, frequency or timing of use
Confidence in the evidence
Low

The second of four GRADE levels, the effect estimate is of limited reliability.

Quality profile
Sample size
Blinding
Effect size No benefit
Citations / year
Authors
Rosenblatt KA, Daling JR, Chen C, Sherman KJ, Schwartz SM.
DOI 10.1158/0008-5472.can-03-3425
Design: Bevölkerungsbasierte Fall-Kontroll-Studie
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Abstract
Previous laboratory investigations, case reports, and a hospital-based case-control study have suggested that Cannabis use may be a risk factor for squamous cell head and neck cancer. We conducted a population-based case-control study to determine whether Cannabis use is associated with the development of oral squamous cell carcinoma (OSCC). Case subjects (n = 407) were 18-65-year-old residents of three counties in western Washington State who were newly diagnosed with OSCC from 1985 through 1995. Control subjects (n = 615), who were similar to the cases with respect to age and sex, were selected from the general population using random-digit telephone dialing. Lifetime histories of Cannabis use and exposure to known OSCC risk factors were ascertained using a structured questionnaire. Information on genetic polymorphisms in glutathione S-transferase enzymes was obtained from assays on participant DNA. Odds ratios for associations with features of Cannabis use were adjusted for sex, education, birth year, alcohol consumption, and cigarette smoking. A similar proportion of case subjects (25.6%) and control subjects (24.4%) reported ever use of Cannabis (adjusted odds ratio, 0.9; 95% confidence interval, 0.6-1.3). There were no trends in risk observed with increasing duration or average frequency of use or time since first or last use. No subgroup defined by known or suspected OSCC risk factors (age, cigarette smoking, alcohol consumption, and genetic polymorphisms) showed an increased risk. Cannabis use was not associated with OSCC risk in this large, population-based study.

The impediment to action advances action. — Marcus Aurelius