CONTRIBUTION OF CADMIUM IN CIGARETTES TO LUNG-CANCER - AN EVALUATION OF RISK ASSESSMENT METHODOLOGIES

This investigation concerned the use of quantitative risk assessment f or estimating cancer mortality at low-level exposures. We empirically tested whether extrapolating by linear no-threshold models predicted i mplausible risks at low-level exposures. Cadmium in cigarette smoke wa s the low-level exposure, and extrapolation was based on potencies est imated from an occupational study and a rodent cancer bioassay. Inhale d cadmium in mainstream and sidestream smoke was estimated from publis hed laboratory experiments. Smoking-specific lung cancer and all-cause mortality rates were estimated from large population-based studies. T he mortality rates, amount of inhaled cadmium, and potency values were used to construct life tables for calculating lifetime lung cancer ri sk with and without a contribution from cadmium in cigarette smoke. Th e epidemiologic data predicted that 1 to 18 lung cancer deaths per 10 000 smokers may be attributable to inhaled cadmium in cigarette smoke, or approximately 0.2% to 1.6% of smoking-induced lung cancer deaths. Upper 95% bounds on these figures are 7 to 95 lung cancer deaths or 1. 6% to 8.8% of smoking-related deaths. The rodent data predicted that 8 0 to 416 lung cancer deaths per 10 000 smokers (95% upper bounds: 136- 707) or 13% to 47% (23-81%) of smoking-induced lung cancer mortality m ay be attributable to cadmium in cigarette smoke. Linear extrapolation from human data appears to provide plausible estimates of risk at low doses. Considering the large number of carcinogens present in cigaret te smoke, the extrapolation from rodents appears to overestimate human risks. Whether this discrepancy resorts from differences in potency f or cadmium chloride aerosol as opposed to cadmium in particulate form, or from humans having greater sensitivity to cadmium's carcinogenic e ffect, or both, remains unclear.