Abstract

Individuals differ in their susceptibility to radiogenic cancers, and there is evidence that this inter-individual susceptibility extends to HZE ion-induced carcinogenesis. Three components of individual risk: sex, age at exposure, and prior tobacco use, are already incorporated into the NASA cancer risk model used to determine safe days in space for US astronauts. Here, we examine other risk factors that could potentially be included in risk calculations. These include personal and family medical history, the presence of pre-malignant cells that could undergo malignant transformation as a consequence of radiation exposure, the results from phenotypic assays of radiosensitivity, heritable genetic polymorphisms associated with radiosensitivity, and postflight monitoring. Inclusion of these additional risk or risk reduction factors has the potential to personalize risk estimates for individual astronauts and could influence the determination of safe days in space. We consider how this type of assessment could be used and explore how the provisions of the federal Genetic Information Non-discrimination Act could impact the collection, dissemination and use of this information by NASA.

Highlights

  • In spaceflight, astronauts are exposed to a radiation environment consisting of a uniform flux of background galactic cosmic radiation with intermittent pulses of high energy protons from solar particle events

  • This article discusses how potential approaches for the detection of inter-individual differences in susceptibility to radiogenic cancer could impinge on the federal Genetic Information Non-discrimination Act of 2008 (GINA) and explores whether an employer (i.e., NASA) could lawfully use the information in employment or work assignment decisions

  • Synopsis Individual risk of radiation carcinogenesis might be more accurately calculated by including family history of cancer and/ or personal medical history including a history of colon polyps or breast biopsies. An assumption in this approach is that breast or colon cancer risk from space radiation exposure can be predicted, at least partly, from background risk by a transfer model incorporating multiplicative risk

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Summary

Personalized Cancer Risk Assessments for Space Radiation

Individuals differ in their susceptibility to radiogenic cancers, and there is evidence that this inter-individual susceptibility extends to HZE ion-induced carcinogenesis. We examine other risk factors that could potentially be included in risk calculations These include personal and family medical history, the presence of pre-malignant cells that could undergo malignant transformation as a consequence of radiation exposure, the results from phenotypic assays of radiosensitivity, heritable genetic polymorphisms associated with radiosensitivity, and postflight monitoring. Inclusion of these additional risk or risk reduction factors has the potential to personalize risk estimates for individual astronauts and could influence the determination of safe days in space.

INTRODUCTION
Personal and Family Medical History
Detection of Preneoplastic Cells and Dormant Microtumors
Phenotypic Assays of Sensitivity
Genotypic Assays of Sensitivity
PostFlight Monitoring
APPLICABILITY OF GINA TO PERSONALIZED CANCER RISK APPROACHES
Overview of GINA
Genotypic assays of sensitivity
Information for Space Radiation Risk
Findings
PostFlight Monitoring and GINA
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