Evidence map›Paper›PMID 24974847›Full record

Trial reportNature genetics2014

A three-stage genome-wide association study identifies a susceptibility locus for late radiotherapy toxicity at 2q24.1.

Laura Fachal, Antonio Gómez-Caamaño, Gillian C Barnett, Paula Peleteiro, Ana M Carballo, Patricia Calvo-Crespo, Sarah L Kerns, Manuel Sánchez-García, Ramón Lobato-Busto, Leila Dorling and 10 more

Open access · greenAbstract readClinical TrialMulticenter StudyRandomized Controlled Trial
PubMed Publisher
In one paragraph

Trial report in Nature genetics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 77 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
77citing papers in PubMed, 5 pooled it
12.0field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

77 citing papers in PubMed, 5 syntheses or guidelines pooled it, 147 citations in OpenAlex.

  1. Pooled it
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  6. Trial
  7. Article
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  9. Review
  10. Novel molecular biomarkers associated with Taxane-induced toxicities in women with breast cancer from the Brazilian Amazon.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
    Article
  11. Remote blood collection among cancer patients and age- and sex-matched controls for biomarker and genetic analyses using the PROFILES registry.Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer · 2026
    Review
  12. Article
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  15. Review
  16. Article
  17. A Polygenic Risk Score for Late Bladder Toxicity Following Radiotherapy for Non-Metastatic Prostate Cancer.Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology · 2025
    Article
  18. Article
  19. Article
  20. Article

17 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

20 authors at 10 institutions in 4 countries.

Laura Fachal1] Fundación Pública Galega de Medicina Xenómica, Servizo Galego de Saúde (SERGAS), Santiago de Compostela, Spain. [2] Grupo de Medicina Xenómica, Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), Universidade de Santiago de Compostela (USC), Santiago de Compostela, Spain.ORCID 0000000272569752
Antonio Gómez-CaamañoDepartment of Radiation Oncology, USC University Hospital Complex, SERGAS, Santiago de Compostela, Spain.
Gillian C BarnettCentre for Cancer Genetic Epidemiology, University of Cambridge, Strangeways Research Laboratory, Cambridge, UK.
Paula PeleteiroDepartment of Radiation Oncology, USC University Hospital Complex, SERGAS, Santiago de Compostela, Spain.
Ana M CarballoDepartment of Radiation Oncology, USC University Hospital Complex, SERGAS, Santiago de Compostela, Spain.
Patricia Calvo-CrespoDepartment of Radiation Oncology, USC University Hospital Complex, SERGAS, Santiago de Compostela, Spain.
Sarah L KernsDepartment of Radiation Oncology, Icahn School of Medicine at Mount Sinai, New York, New York, USA.
Manuel Sánchez-GarcíaDepartment of Medical Physics, USC University Hospital Complex, SERGAS, Santiago de Compostela, Spain.
Ramón Lobato-BustoDepartment of Medical Physics, USC University Hospital Complex, SERGAS, Santiago de Compostela, Spain.
Leila DorlingCentre for Cancer Genetic Epidemiology, University of Cambridge, Strangeways Research Laboratory, Cambridge, UK.
Rebecca M ElliottInstitute of Cancer Sciences, University of Manchester, Manchester Academic Health Science Centre, Christie Hospital, Manchester, UK.
David P DearnaleyInstitute of Cancer Research and Royal Marsden National Health Service (NHS) Foundation Trust, Sutton, UK.
Matthew R SydesCancer and Other Non-Infectious Diseases, Medical Research Council (MRC) Clinical Trials Unit, London, UK.ORCID 0000000293231371
Emma HallClinical Trials and Statistics Unit, Institute of Cancer Research, London, UK.
Neil G BurnetDepartment of Oncology, University of Cambridge, Oncology Centre, Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK.
Ángel Carracedo1] Fundación Pública Galega de Medicina Xenómica, Servizo Galego de Saúde (SERGAS), Santiago de Compostela, Spain. [2] Grupo de Medicina Xenómica, Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), Universidade de Santiago de Compostela (USC), Santiago de Compostela, Spain. [3] Center of Excellence in Genomic Medicine Research (CEGMR), King Abdulaziz University, Jeddah, Saudi Arabia.
Barry S RosensteinDepartment of Radiation Oncology, Icahn School of Medicine at Mount Sinai, New York, New York, USA.
Catharine M L WestInstitute of Cancer Sciences, University of Manchester, Manchester Academic Health Science Centre, Christie Hospital, Manchester, UK.
Alison M DunningCentre for Cancer Genetic Epidemiology, University of Cambridge, Strangeways Research Laboratory, Cambridge, UK.
Ana Vega1] Fundación Pública Galega de Medicina Xenómica, Servizo Galego de Saúde (SERGAS), Santiago de Compostela, Spain. [2] Grupo de Medicina Xenómica, Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), Universidade de Santiago de Compostela (USC), Santiago de Compostela, Spain.
Complejo Hospitalario Universitario de Santiago · ESUniversity of Cambridge · GBIcahn School of Medicine at Mount Sinai · USManchester Academic Health Science Centre · GBFundación Pública Galega de Medicina Xenómica · ESInstitute of Cancer Research · GBKing Abdulaziz University · SAMRC Clinical Trials Unit at UCL · GBNational Health Service · GBUniversidade de Santiago de Compostela · ES

Funding

Genome-Wide Study to Identify SNPs and CNPs Associated with Radiation InjuryR01CA134444 · NCI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI OSTRER, HARRY, ROSENSTEIN, BARRY S · 2009 to 2012
$2.3M
Arthritis Research UK C8262/A7253Cancer Research UK 10588Cancer Research UK 16565Cancer Research UK 18504Cancer Research UK 7253Cancer Research UK SP2312/021Department of HealthMedical Research Council MC_U122861330Medical Research Council MC_UU_12023/6NCI NIH HHS 1R01CA134444NCI NIH HHS R01 CA134444
6 · The paper itself

Abstract

There is increasing evidence supporting the role of genetic variants in the development of radiation-induced toxicity. However, previous candidate gene association studies failed to elucidate the common genetic variation underlying this phenotype, which could emerge years after the completion of treatment. We performed a genome-wide association study on a Spanish cohort of 741 individuals with prostate cancer treated with external beam radiotherapy (EBRT). The replication cohorts consisted of 633 cases from the UK and 368 cases from North America. One locus comprising TANC1 (lowest unadjusted P value for overall late toxicity=6.85×10(-9), odds ratio (OR)=6.61, 95% confidence interval (CI)=2.23-19.63) was replicated in the second stage (lowest unadjusted P value for overall late toxicity=2.08×10(-4), OR=6.17, 95% CI=2.25-16.95; Pcombined=4.16×10(-10)). The inclusion of the third cohort gave unadjusted Pcombined=4.64×10(-11). These results, together with the role of TANC1 in regenerating damaged muscle, suggest that the TANC1 locus influences the development of late radiation-induced damage.

Indexed as

Chromosomes, Human, Pair 2Genetic LociGenetic Predisposition to DiseaseGenome-Wide Association StudyHumansMalePolymorphism, Single NucleotideProstatic NeoplasmsRadiation InjuriesRadiotherapySpain

Identifiers

PMID24974847
OpenAlexW2006988918

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.