Paula Peleteiro

ORCID: 0000-0002-8900-2541
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About
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Research Areas
  • Prostate Cancer Treatment and Research
  • Advanced Radiotherapy Techniques
  • Prostate Cancer Diagnosis and Treatment
  • Effects of Radiation Exposure
  • Radiopharmaceutical Chemistry and Applications
  • Advances in Oncology and Radiotherapy
  • Gastric Cancer Management and Outcomes
  • Lung Cancer Diagnosis and Treatment
  • Genetic factors in colorectal cancer
  • BRCA gene mutations in cancer
  • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
  • Cancer-related molecular mechanisms research
  • Genetic Associations and Epidemiology
  • Medical Imaging Techniques and Applications
  • Colorectal Cancer Treatments and Studies
  • Colorectal Cancer Surgical Treatments
  • Cancer, Lipids, and Metabolism
  • Global Cancer Incidence and Screening
  • Hepatocellular Carcinoma Treatment and Prognosis
  • Molecular Biology Techniques and Applications
  • Radiation Therapy and Dosimetry
  • Colorectal and Anal Carcinomas
  • Korean Peninsula Historical and Political Studies
  • Inflammatory Bowel Disease
  • Intraperitoneal and Appendiceal Malignancies

Complejo Hospitalario Universitario de Santiago
2013-2025

Servicio Gallego de Salud
2011-2025

Universidade de Santiago de Compostela
2025

Instituto de Investigación Sanitaria de Santiago
2023-2025

Complexo Hospitalario Universitario A Coruña
2011-2023

Abstract Background A total of 10%–20% patients develop long-term toxicity following radiotherapy for prostate cancer. Identification common genetic variants associated with susceptibility to radiotoxicity might improve risk prediction and inform functional mechanistic studies. Methods We conducted an individual patient data meta-analysis six genome-wide association studies (n = 3871) in men European ancestry who underwent Radiotoxicities (increased urinary frequency, decreased stream,...

10.1093/jnci/djz075 article EN cc-by JNCI Journal of the National Cancer Institute 2019-05-07
Petra Seibold Adam Webb Miguel E. Aguado‐Barrera D. Azria C. Bourgier and 95 more Muriel Brengues Erik Briers Renée Bultijnck Patricia Calvo Ana Carballo Ananya Choudhury A. Cicchetti Johannes Claßen E. Delmastro Alison M. Dunning Rebecca M. Elliott Laura Fachal Marie‐Pierre Farcy‐Jacquet P. Gabriele E. Garibaldi Antonio Gómez‐Caamaño Sara Gutiérrez‐Enríquez Daniel S. Higginson Kerstie Johnson Ramón Lobato-Busto Meritxell Mollà Anusha Müller Debbie Payne Paula Peleteiro Giselle Post T. Rancati Tim Rattay Victoria Reyes Barry S. Rosenstein Dirk De Ruysscher Maria Carmen De Santis Jörg Schäfer Thomas Schnabel Elena Sperk R.P. Symonds Hilary Stobart Begoña Taboada‐Valladares Chris J. Talbot R. Valdagni Ana Vega Liv Veldeman Tim Ward Christian Weißenberger Catharine West Jenny Chang‐Claude Yolande Lievens M. Van Eijkeren Katrien Vandecasteele Elhaseen Elhamin Piet Ost Valérie Fonteyne Martijn Swimberghe Pieter Deseyne Wilfried De Neve Fréderic Duprez Marcus Mareel Chris Monten Annick Van Greveling Tom Vercauteren Leen Paelinck Gilles Defraene Rita Aerts Soumia Arredouani Maarten Lambrecht Ben Vanneste Roxana Draghici Frank A. Giordano Carsten Herskind Marlon R. Veldwijk Irmgard Helmbold Ulrich Giesche Petra Stegmaier Christian Weiß Thomas Blaschke Burkhard Neu Laura Lozza B. Avuzzi S. Morlino Claudia Sangalli Marzia Franceschini Belina Rodriguez-Lage Juan Fernández‐Tajes Olivia Fuentes-Ríos Isabel Domínguez-Rios Irene Fajardo-Paneque Paloma Sosa‐Fajardo Laura Torrado-Moya Mónica Ramos-Albiac Alexandra Giraldo M. Altabas Bibiana Piqué-Leiva David García-Relancio Alejandro Seoane-Ramallo Samuel Lavers Simon K. Wright

REQUITE aimed to establish a resource for multi-national validation of models and biomarkers that predict risk late toxicity following radiotherapy. The purpose this article is provide summary descriptive data.

10.1016/j.radonc.2019.04.034 article EN cc-by-nc-nd Radiotherapy and Oncology 2019-05-27

Abstract Background: Late bladder toxicity is a concern for patients receiving prostate cancer radiotherapy and negatively impacts survivors. Few risk factors are known beyond the radiation dose volume of exposed. A polygenic score (PRS) could identify susceptible patients. Methods: PRS was built using genome-wide association results from Radiogenomics Consortium (N=3,988), then tested in prospective REQUITE URWCI studies (N=2,034). The primary outcome time-to-patient-reported gross (≥ grade...

10.1158/1055-9965.epi-24-1228 article EN Cancer Epidemiology Biomarkers & Prevention 2025-03-03

Prostate cancer is the second most common globally, with radiation therapy (RT) being a key treatment for clinically localized and locally advanced cases. Given high survival rates, addressing long-term side effects of RT crucial preserving quality-of-life. Radiogenomics, study genetic variations affecting response to radiation, has primarily focussed on genomic biomarkers, while DNA methylation studies offer insights into responses. Although research centred tumours, no epigenome-wide...

10.1186/s13148-025-01846-8 article EN cc-by-nc-nd Clinical Epigenetics 2025-03-06

10.1016/j.rpor.2013.03.681 article EN publisher-specific-oa Reports of Practical Oncology & Radiotherapy 2013-06-01

e16530 Background: Changes in PSA are widely used as a biomarker for the monitoring of treatment outcome Metastatic Castration-Resistant Prostate Cancer (mCRPC) clinical real-world setting. Early changes (before 12 weeks) not considered definition Progression (PSAProg) due to potential spurious “flare” reactions. We aimed evaluate significance an early increase Abiraterone/Enzalutamide (Abi/Enz)-treated mCRPC patients (pts). Methods: retrospectively evaluated Abi/Enz-treated pts from 11...

10.1200/jco.2019.37.15_suppl.e16530 article EN Journal of Clinical Oncology 2019-05-20
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