J Natl Cancer Inst Monogr. 2020 Jul 1;2020(56):188-200. doi: 10.1093/jncimonographs/lgaa010.
Ionizing radiation is an established carcinogen, but risks from low-dose exposures are controversial. Since the Biological Effects of Ionizing Radiation VII review of the epidemiological data in 2006, many subsequent publications have reported excess cancer risks from low-dose exposures. Our aim was to systematically review these studies to assess the magnitude of the risk and whether the positive findings could be explained by biases.
Eligible studies had mean cumulative doses of less than 100 mGy, individualized dose estimates, risk estimates, and confidence intervals (CI) for the dose-response and were published in 2006-2017. We summarized the evidence for bias (dose error, confounding, outcome ascertainment) and its likely direction for each study. We tested whether the median excess relative risk (ERR) per unit dose equals zero and assessed the impact of excluding positive studies with potential bias away from the null. We performed a meta-analysis to quantify the ERR and assess consistency across studies for all solid cancers and leukemia.
Of the 26 eligible studies, 8 concerned environmental, 4 medical, and 14 occupational exposure. For solid cancers, 16 of 22 studies reported positive ERRs per unit dose, and we rejected the hypothesis that the median ERR equals zero (P = .03). After exclusion of 4 positive studies with potential positive bias, 12 of 18 studies reported positive ERRs per unit dose (P = .12). For leukemia, 17 of 20 studies were positive, and we rejected the hypothesis that the median ERR per unit dose equals zero (P = .001), also after exclusion of 5 positive studies with potential positive bias (P = .02). For adulthood exposure, the meta-ERR at 100 mGy was 0.029 (95% CI = 0.011 to 0.047) for solid cancers and 0.16 (95% CI = 0.07 to 0.25) for leukemia. For childhood exposure, the meta-ERR at 100 mGy for leukemia was 2.84 (95% CI = 0.37 to 5.32); there were only two eligible studies of all solid cancers.
Our systematic assessments in this monograph showed that these new epidemiological studies are characterized by several limitations, but only a few positive studies were potentially biased away from the null. After exclusion of these studies, the majority of studies still reported positive risk estimates. We therefore conclude that these new epidemiological studies directly support excess cancer risks from low-dose ionizing radiation. Furthermore, the magnitude of the cancer risks from these low-dose radiation exposures was statistically compatible with the radiation dose-related cancer risks of the atomic bomb survivors.
电离辐射是一种已确定的致癌物质,但低剂量暴露的风险仍存在争议。自 2006 年《电离辐射生物学效应》第七次审查流行病学数据以来,许多后续出版物报告了低剂量暴露致癌风险的增加。我们的目的是系统地审查这些研究,以评估风险的大小,以及阳性结果是否可以用偏倚来解释。
合格的研究具有低于 100 mGy 的平均累积剂量、个体化剂量估计、剂量反应的风险估计和置信区间 (CI),并于 2006 年至 2017 年发表。我们总结了每个研究中存在的偏倚 (剂量误差、混杂、结局确定) 的证据及其可能的方向。我们检验了单位剂量的中位超额相对风险 (ERR) 是否等于零,并评估了排除有潜在偏倚的阳性研究对零假设的影响。我们进行了荟萃分析,以量化所有实体癌和白血病的 ERR,并评估研究之间的一致性。
在 26 项合格研究中,8 项涉及环境暴露,4 项涉及医疗暴露,14 项涉及职业暴露。对于实体癌,22 项研究中有 16 项报告了单位剂量的阳性 ERR,我们拒绝了中位 ERR 等于零的假设 (P =.03)。排除 4 项有潜在阳性偏倚的阳性研究后,18 项研究中有 12 项报告了单位剂量的阳性 ERR (P = .12)。对于白血病,20 项研究中有 17 项为阳性,我们拒绝了中位 ERR 等于零的假设 (P =.001),也排除了 5 项有潜在阳性偏倚的阳性研究 (P = .02)。对于成人暴露,100 mGy 时的荟萃 ERR 为 0.029 (95%CI = 0.011 至 0.047),用于实体癌,0.16 (95%CI = 0.07 至 0.25),用于白血病。对于儿童暴露,100 mGy 时白血病的荟萃 ERR 为 2.84 (95%CI = 0.37 至 5.32);仅有两项合格的所有实体癌研究。
本专题的系统评估表明,这些新的流行病学研究具有几个局限性,但只有少数阳性研究可能存在偏离零假设的偏倚。排除这些研究后,大多数研究仍报告阳性风险估计。因此,我们得出结论,这些新的流行病学研究直接支持低剂量电离辐射致癌风险的增加。此外,这些低剂量辐射暴露的癌症风险的大小在统计学上与原子弹幸存者的辐射剂量相关癌症风险相吻合。