Abstract

BackgroundPrevious studies have shown that acute external in utero exposure to ionizing radiation can increase cancer risk. It is not known whether chronic exposure at low dose rates, including due to radionuclide intake, influences the lifetime risk of solid cancers in the offspring. The objective of this study was to investigate solid cancer risk after in utero irradiation.MethodsCancer incidence and mortality over a 60-year period (from January 1950 to December 2009) were analyzed in the Urals Prenatally Exposed Cohort (UPEC). The cohort comprised in utero exposed offspring of Mayak Production Association female workers and of female residents of Techa River villages. Some of the offspring also received postnatal exposure, either due to becoming radiation workers themselves or due to continuing to live in the contaminated areas of the Techa River. The mortality analyses comprised 16,821 subjects (601,372 person-years), and the incidence analyses comprised 15,813 subjects (554,411 person-years). Poisson regression was used to quantify the relative risk as a function of the in utero soft tissue dose (with cumulative doses up to 944.9 mGy, mean dose of 14.1 mGy in the pooled cohort) and the postnatal stomach dose for solid cancer incidence and mortality.ResultsWhen a log-linear model was used, relative risk of cancer per 10 mGy of in utero dose was 0.99 (95% confidence interval (CI) = 0.96 to 1.01) based on incidence data and 0.98 (CI = 0.94 to 1.01) based on mortality data. Postnatal exposure to ionizing radiation was positively associated with the solid cancer risk in members of the UPEC, with a relative risk of 1.02 per 10mGy CI = 1.00 to 1.04).ConclusionsNo strong evidence was found that chronic low-dose-rate exposure of the embryo and fetus increased the risk of solid cancers in childhood or in adulthood. For both incidence and mortality, a tendency towards a decreased relative risk was noted with increasing doses to soft tissues of the fetus. Further follow-up will provide more precise radiation risk estimates of solid cancer as cohort members are approaching their 60s and cancer becomes more common.

Highlights

  • The high proliferative and differential potential of embryonic and fetal cells and tissues is suggestive of elevated carcinogenic radiosensitivity of the prenatal organism

  • Poisson regression was used to quantify the relative risk as a function of the in utero soft tissue dose and the postnatal stomach dose for solid cancer incidence and mortality

  • No strong evidence was found that chronic low-dose-rate exposure of the embryo and fetus increased the risk of solid cancers in childhood or in adulthood

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Summary

Introduction

The high proliferative and differential potential of embryonic and fetal cells and tissues is suggestive of elevated carcinogenic radiosensitivity of the prenatal organism. The main limitation of previous studies is inadequate statistical power because of the small sample sizes and the small number of observed cancer cases [4]. It is unknown at present whether chronic exposure at low dose rates, including that caused by the ingress of radionuclides into the bodies of pregnant women, can influence the risk of solid cancers in their offspring. Previous studies have shown that acute external in utero exposure to ionizing radiation can increase cancer risk It is not known whether chronic exposure at low dose rates, including due to radionuclide intake, influences the lifetime risk of solid cancers in the offspring. The objective of this study was to investigate solid cancer risk after in utero irradiation

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