Literature DB >> 19454801

Mammography-oncogenecity at low doses.

G J Heyes1, A J Mill, M W Charles.   

Abstract

Controversy exists regarding the biological effectiveness of low energy x-rays used for mammography breast screening. Recent radiobiology studies have provided compelling evidence that these low energy x-rays may be 4.42 +/- 2.02 times more effective in causing mutational damage than higher energy x-rays. These data include a study involving in vitro irradiation of a human cell line using a mammography x-ray source and a high energy source which matches the spectrum of radiation observed in survivors from the Hiroshima atomic bomb. Current radiation risk estimates rely heavily on data from the atomic bomb survivors, and a direct comparison between the diagnostic energies used in the UK breast screening programme and those used for risk estimates can now be made. Evidence highlighting the increase in relative biological effectiveness (RBE) of mammography x-rays to a range of x-ray energies implies that the risks of radiation-induced breast cancers for mammography x-rays are potentially underestimated by a factor of four. A pooled analysis of three measurements gives a maximal RBE (for malignant transformation of human cells in vitro) of 4.02 +/- 0.72 for 29 kVp (peak accelerating voltage) x-rays compared to high energy electrons and higher energy x-rays. For the majority of women in the UK NHS breast screening programme, it is shown that the benefit safely exceeds the risk of possible cancer induction even when this higher biological effectiveness factor is applied. The risk/benefit analysis, however, implies the need for caution for women screened under the age of 50, and particularly for those with a family history (and therefore a likely genetic susceptibility) of breast cancer. In vitro radiobiological data are generally acquired at high doses, and there are different extrapolation mechanisms to the low doses seen clinically. Recent low dose in vitro data have indicated a potential suppressive effect at very low dose rates and doses. Whilst mammography is a low dose exposure, it is not a low dose rate examination, and protraction of dose should not be confused with fractionation. Although there is potential for a suppressive effect at low doses, recent epidemiological data, and several international radiation risk assessments, continue to promote the linear no-threshold (LNT) model. Finally, recent studies have shown that magnetic resonance imaging (MRI) is more sensitive than mammography in detecting invasive breast cancer in women with a genetic sensitivity. Since an increase in the risk associated with mammographic screening would blur the justification of exposure for this high risk subgroup, the use of other (non-ionising) screening modalities is preferable.

Entities:  

Mesh:

Year:  2009        PMID: 19454801     DOI: 10.1088/0952-4746/29/2A/S08

Source DB:  PubMed          Journal:  J Radiol Prot        ISSN: 0952-4746            Impact factor:   1.394


  10 in total

1.  DNA double strand breaks induced by low dose mammography X-rays in breast tissue: A pilot study.

Authors:  Julie Depuydt; Tanguy Viaene; Phillip Blondeel; Nathalie Roche; Rudy Van den Broecke; Hubert Thierens; Anne Vral
Journal:  Oncol Lett       Date:  2018-06-26       Impact factor: 2.967

2.  Impact of the digitalisation of mammography on performance parameters and breast dose in the Flemish Breast Cancer Screening Programme.

Authors:  Lore Timmermans; An De Hauwere; Klaus Bacher; Hilde Bosmans; Kim Lemmens; Luc Bleyen; Erik Van Limbergen; Patrick Martens; Andre Van Steen; Griet Mortier; Koen Van Herck; Hubert Thierens
Journal:  Eur Radiol       Date:  2014-05-10       Impact factor: 5.315

3.  Radiation risk of breast screening in England with digital mammography.

Authors:  Lucy M Warren; David R Dance; Kenneth C Young
Journal:  Br J Radiol       Date:  2016-09-21       Impact factor: 3.039

Review 4.  State of the evidence 2017: an update on the connection between breast cancer and the environment.

Authors:  Janet M Gray; Sharima Rasanayagam; Connie Engel; Jeanne Rizzo
Journal:  Environ Health       Date:  2017-09-02       Impact factor: 5.984

5.  Integrating mammographic breast density in glandular dose calculation.

Authors:  Moayyad E Suleiman; Patrick C Brennan; Ernest Ekpo; Peter Kench; Mark F McEntee
Journal:  Br J Radiol       Date:  2018-02-13       Impact factor: 3.039

Review 6.  Novel drugs that target the estrogen-related receptor alpha: their therapeutic potential in breast cancer.

Authors:  Felicity Eb May
Journal:  Cancer Manag Res       Date:  2014-05-23       Impact factor: 3.989

7.  Breast cancer detection among young survivors of pediatric Hodgkin lymphoma with screening magnetic resonance imaging.

Authors:  Minh Thi Tieu; Candemir Cigsar; Sameera Ahmed; Andrea Ng; Lisa Diller; B-A Millar; Pavel Crystal; David C Hodgson
Journal:  Cancer       Date:  2014-05-28       Impact factor: 6.860

8.  Increased chromosomal radiosensitivity in asymptomatic carriers of a heterozygous BRCA1 mutation.

Authors:  Annelot Baert; Julie Depuydt; Tom Van Maerken; Bruce Poppe; Fransiska Malfait; Katrien Storm; Jenneke van den Ende; Tim Van Damme; Sylvia De Nobele; Gianpaolo Perletti; Kim De Leeneer; Kathleen B M Claes; Anne Vral
Journal:  Breast Cancer Res       Date:  2016-05-17       Impact factor: 6.466

9.  Counselees' Expressed Level of Understanding of the Risk Estimate and Surveillance Recommendation are Not Associated with Breast Cancer Surveillance Adherence.

Authors:  Akke Albada; Sandra van Dulmen; Henrietta Dijkstra; Ivette Wieffer; Arjen Witkamp; Margreet G E M Ausems
Journal:  J Genet Couns       Date:  2015-09-01       Impact factor: 2.537

10.  Effective dose in medicine.

Authors:  C J Martin
Journal:  Ann ICRP       Date:  2020-11-04
  10 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.