Cancer risks attributable to low doses of ionizing radiation: assessing what we really know

David J Brenner, Richard Doll, Dudley T Goodhead, Eric J Hall, Charles E Land, John B Little, Jay H Lubin, Dale L Preston, R Julian Preston, Jerome S Puskin, Elaine Ron, Rainer K Sachs, Jonathan M Samet, Richard B Setlow, Marco Zaider, David J Brenner, Richard Doll, Dudley T Goodhead, Eric J Hall, Charles E Land, John B Little, Jay H Lubin, Dale L Preston, R Julian Preston, Jerome S Puskin, Elaine Ron, Rainer K Sachs, Jonathan M Samet, Richard B Setlow, Marco Zaider

Abstract

High doses of ionizing radiation clearly produce deleterious consequences in humans, including, but not exclusively, cancer induction. At very low radiation doses the situation is much less clear, but the risks of low-dose radiation are of societal importance in relation to issues as varied as screening tests for cancer, the future of nuclear power, occupational radiation exposure, frequent-flyer risks, manned space exploration, and radiological terrorism. We review the difficulties involved in quantifying the risks of low-dose radiation and address two specific questions. First, what is the lowest dose of x- or gamma-radiation for which good evidence exists of increased cancer risks in humans? The epidemiological data suggest that it is approximately 10-50 mSv for an acute exposure and approximately 50-100 mSv for a protracted exposure. Second, what is the most appropriate way to extrapolate such cancer risk estimates to still lower doses? Given that it is supported by experimentally grounded, quantifiable, biophysical arguments, a linear extrapolation of cancer risks from intermediate to very low doses currently appears to be the most appropriate methodology. This linearity assumption is not necessarily the most conservative approach, and it is likely that it will result in an underestimate of some radiation-induced cancer risks and an overestimate of others.

Figures

Fig. 1.
Fig. 1.
Size of a cohort exposed to different radiation doses, which would be required to detect a significant increase in cancer mortality in that cohort, assuming lifetime follow-up (9).
Fig. 2.
Fig. 2.
Estimated excess relative risk (±1 SE) of mortality (1950–1997) from solid cancers among groups of survivors in the LSS cohort of atomic bomb survivors, who were exposed to low doses (P = 0.15 and 0.3, respectively) compared with the comparison population who were exposed to <5 mSv, whereas the remaining four higher-dose points (in red) are statistically significant (P < 0.05). The dashed straight line represents the results of a linear fit (2) to all the data from 5 to 4,000 mSv (higher dose points are not shown).
Fig. 3.
Fig. 3.
Schematic representation of different possible extrapolations of measured radiation risks down to very low doses, all of which could, in principle, be consistent with higher-dose epidemiological data. Curve a, linear extrapolation; curve b, downwardly curving (decreasing slope); curve c, upwardly curving (increasing slope); curve d, threshold; curve e, hormetic.
Fig. 4.
Fig. 4.
Estimated risks (relative to an unexposed individual) of solid cancer in atomic bomb survivors exposed to low radiation doses (12). Data points are placed at the mean of each dose category. The solid curve represents a weighted moving average of the points shown (dotted curves: ±1 SE), and the dashed straight line is a linear risk estimate computed from all the data in the dose range from 0 to 2,000 mSv. Age-specific cancer rates from 1958 to 1994 are used, averaged over follow-up and gender.
Fig. 5.
Fig. 5.
Schematic representation of the potential effect of a small (0.25%) population of women, who are extremely sensitive for radiation-induced breast cancer, compared with the general (normal) population. Schematized is the number of radiation-induced breast cancers as a percentage of the overall population. The dose–risk relations for both the normal and the sensitive populations are assumed to be linear. Because the number of radiation-induced breast cancers in the sensitive population would saturate as the dose increases (because all the exposed women would have developed breast cancer), the dose–response for the whole population would be downwardly curving.

Source: PubMed

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