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Verfasst von:Webb, Adam J. [VerfasserIn]   i
 Harper, Emily [VerfasserIn]   i
 Rattay, Tim [VerfasserIn]   i
 Aguado-Barrera, Miguel E. [VerfasserIn]   i
 Azria, David [VerfasserIn]   i
 Bourgier, Celine [VerfasserIn]   i
 Brengues, Muriel [VerfasserIn]   i
 Briers, Erik [VerfasserIn]   i
 Bultijnck, Renée [VerfasserIn]   i
 Chang-Claude, Jenny [VerfasserIn]   i
 Choudhury, Ananya [VerfasserIn]   i
 Cicchetti, Alessandro [VerfasserIn]   i
 De Ruysscher, Dirk [VerfasserIn]   i
 De Santis, Maria Carmen [VerfasserIn]   i
 Dunning, Alison M. [VerfasserIn]   i
 Elliott, Rebecca M. [VerfasserIn]   i
 Fachal, Laura [VerfasserIn]   i
 Gómez-Caamaño, Antonio [VerfasserIn]   i
 Gutiérrez-Enríquez, Sara [VerfasserIn]   i
 Johnson, Kerstie [VerfasserIn]   i
 Lobato-Busto, Ramón [VerfasserIn]   i
 Kerns, Sarah L. [VerfasserIn]   i
 Post, Giselle [VerfasserIn]   i
 Rancati, Tiziana [VerfasserIn]   i
 Reyes, Victoria [VerfasserIn]   i
 Rosenstein, Barry S. [VerfasserIn]   i
 Seibold, Petra Beate [VerfasserIn]   i
 Seoane, Alejandro [VerfasserIn]   i
 Sosa-Fajardo, Paloma [VerfasserIn]   i
 Sperk, Elena [VerfasserIn]   i
 Taboada-Valladares, Begoña [VerfasserIn]   i
 Valdagni, Riccardo [VerfasserIn]   i
 Vega, Ana [VerfasserIn]   i
 Veldeman, Liv [VerfasserIn]   i
 Ward, Tim [VerfasserIn]   i
 West, Catharine M. [VerfasserIn]   i
 Symonds, R. Paul [VerfasserIn]   i
 Talbot, Christopher J. [VerfasserIn]   i
Titel:Treatment time and circadian genotype interact to influence radiotherapy side-effects
Titelzusatz:a prospective European validation study using the REQUITE cohort
Verf.angabe:Adam J. Webb, Emily Harper, Tim Rattay, Miguel E. Aguado-Barrera, David Azria, Celine Bourgier, Muriel Brengues, Erik Briers, Renée Bultijnck, Jenny Chang-Claude, Ananya Choudhury, Alessandro Cicchetti, Dirk De Ruysscher, Maria Carmen De Santis, Alison M. Dunning, Rebecca M. Elliott, Laura Fachal, Antonio Gómez-Caamaño, Sara Gutiérrez-Enríquez, Kerstie Johnson, Ramón Lobato-Busto, Sarah L. Kerns, Giselle Post, Tiziana Rancati, Victoria Reyes, Barry S. Rosenstein, Petra Seibold, Alejandro Seoane, Paloma Sosa-Fajardo, Elena Sperk, Begoña Taboada-Valladares, Riccardo Valdagni, Ana Vega, Liv Veldeman, Tim Ward, Catharine M. West, R. Paul Symonds, Christopher J. Talbot, the Requite Consortium
E-Jahr:2022
Jahr:[October 2022]
Umfang:16 S.
Illustrationen:Diagramme
Fussnoten:Published online 18 September 2022 ; Gesehen am 20.02.2023
Titel Quelle:Enthalten in: EBioMedicine
Ort Quelle:Amsterdam [u.a.] : Elsevier, 2014
Jahr Quelle:2022
Band/Heft Quelle:84(2022) vom: Okt., Artikel-ID 104269, Seite 1-16
ISSN Quelle:2352-3964
Abstract:Background - Circadian rhythm impacts broad biological processes, including response to cancer treatment. Evidence conflicts on whether treatment time affects risk of radiotherapy side-effects, likely because of differing time analyses and target tissues. We previously showed interactive effects of time and genotypes of circadian genes on late toxicity after breast radiotherapy and aimed to validate those results in a multi-centre cohort. - Methods - Clinical and genotype data from 1690 REQUITE breast cancer patients were used with erythema (acute; n=340) and breast atrophy (two years post-radiotherapy; n=514) as primary endpoints. Local datetimes per fraction were converted into solar times as predictors. Genetic chronotype markers were included in logistic regressions to identify primary endpoint predictors. - Findings - Significant predictors for erythema included BMI, radiation dose and PER3 genotype (OR 1.27(95%CI 1.03-1.56); P < 0.03). Effect of treatment time effect on acute toxicity was inconclusive, with no interaction between time and genotype. For late toxicity (breast atrophy), predictors included BMI, radiation dose, surgery type, treatment time and SNPs in CLOCK (OR 0.62 (95%CI 0.4-0.9); P < 0.01), PER3 (OR 0.65 (95%CI 0.44-0.97); P < 0.04) and RASD1 (OR 0.56 (95%CI 0.35-0.89); P < 0.02). There was a statistically significant interaction between time and genotypes of circadian rhythm genes (CLOCK OR 1.13 (95%CI 1.03-1.23), P < 0.01; PER3 OR 1.1 (95%CI 1.01-1.2), P < 0.04; RASD1 OR 1.15 (95%CI 1.04-1.28), P < 0.008), with peak time for toxicity determined by genotype. - Interpretation - Late atrophy can be mitigated by selecting optimal treatment time according to circadian genotypes (e.g. treat PER3 rs2087947C/C genotypes in mornings; T/T in afternoons). We predict triple-homozygous patients (14%) reduce chance of atrophy from 70% to 33% by treating in mornings as opposed to mid-afternoon. Future clinical trials could stratify patients treated at optimal times compared to those scheduled normally. - Funding - EU-FP7.
DOI:doi:10.1016/j.ebiom.2022.104269
URL:Bitte beachten Sie: Dies ist ein Bibliographieeintrag. Ein Volltextzugriff für Mitglieder der Universität besteht hier nur, falls für die entsprechende Zeitschrift/den entsprechenden Sammelband ein Abonnement besteht oder es sich um einen OpenAccess-Titel handelt.

Volltext: https://doi.org/10.1016/j.ebiom.2022.104269
 Volltext: https://www.sciencedirect.com/science/article/pii/S2352396422004510
 DOI: https://doi.org/10.1016/j.ebiom.2022.104269
Datenträger:Online-Ressource
Sprache:eng
Sach-SW:Breast cancer
 Circadian rhythm
 Genetics
 Radiotherapy
K10plus-PPN:1837127654
Verknüpfungen:→ Zeitschrift

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