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Frontline and Relapsed Rhabdomyosarcoma (FAR-RMS) Clinical Trial: A Report from the European Paediatric Soft Tissue Sarcoma Study Group (EpSSG).
Chisholm, Julia; Mandeville, Henry; Adams, Madeleine; Minard-Collin, Veronique; Rogers, Timothy; Kelsey, Anna; Shipley, Janet; van Rijn, Rick R; de Vries, Isabelle; van Ewijk, Roelof; de Keizer, Bart; Gatz, Susanne A; Casanova, Michela; Hjalgrim, Lisa Lyngsie; Firth, Charlotte; Wheatley, Keith; Kearns, Pamela; Liu, Wenyu; Kirkham, Amanda; Rees, Helen; Bisogno, Gianni; Wasti, Ajla; Wakeling, Sara; Heenen, Delphine; Tweddle, Deborah A; Merks, Johannes H M; Jenney, Meriel.
Afiliación
  • Chisholm J; Children and Young People's Unit, Royal Marsden Hospital and Institute of Cancer Research, Sutton SM2 5PT, UK.
  • Mandeville H; Children and Young People's Unit, Royal Marsden Hospital and Institute of Cancer Research, Sutton SM2 5PT, UK.
  • Adams M; Children's Hospital for Wales, Cardiff CF14 4XW, UK.
  • Minard-Collin V; Department of Paediatric Oncology, Gustave Roussy, 75015 Paris, France.
  • Rogers T; Department of Paediatric Surgery, University Hospitals Bristol and Weston NHS Foundation Trust, Bristol BS1 3NU, UK.
  • Kelsey A; Department of Paediatric Histopathology, Royal Manchester Children's Hospital, Manchester University NHS Foundation Trust, Manchester M13 9WL, UK.
  • Shipley J; The Institute of Cancer Research, London SW7 3RP, UK.
  • van Rijn RR; Department of Radiology and Nuclear Medicine, University of Amsterdam, Amsterdam UMC, 1081 HV Amsterdam, The Netherlands.
  • de Vries I; Princess Máxima Center for Pediatric Oncology, 3584 CS Utrecht, The Netherlands.
  • van Ewijk R; Princess Máxima Center for Pediatric Oncology, 3584 CS Utrecht, The Netherlands.
  • de Keizer B; Princess Máxima Center for Pediatric Oncology, 3584 CS Utrecht, The Netherlands.
  • Gatz SA; Birmingham Women's and Children's NHS Foundation Trust, Birmingham B15 2TG, UK.
  • Casanova M; Cancer Research UK Clinical Trials Unit, Institute of Cancer and Genomic Sciences, University of Birmingham, Birmingham B15 2TT, UK.
  • Hjalgrim LL; Fondazione IRCCS Istituto Nazionale Tumori, 20133 Milan, Italy.
  • Firth C; University Hospital Copenhagen, DK-2200 Copenhagen, Denmark.
  • Wheatley K; Cancer Research UK Clinical Trials Unit, Institute of Cancer and Genomic Sciences, University of Birmingham, Birmingham B15 2TT, UK.
  • Kearns P; Cancer Research UK Clinical Trials Unit, Institute of Cancer and Genomic Sciences, University of Birmingham, Birmingham B15 2TT, UK.
  • Liu W; Cancer Research UK Clinical Trials Unit, Institute of Cancer and Genomic Sciences, University of Birmingham, Birmingham B15 2TT, UK.
  • Kirkham A; Cancer Research UK Clinical Trials Unit, Institute of Cancer and Genomic Sciences, University of Birmingham, Birmingham B15 2TT, UK.
  • Rees H; Cancer Research UK Clinical Trials Unit, Institute of Cancer and Genomic Sciences, University of Birmingham, Birmingham B15 2TT, UK.
  • Bisogno G; Department of Paediatric Oncology, University Hospitals Bristol and Weston NHS Foundation Trust, Bristol BS1 3NU, UK.
  • Wasti A; Department of Women and Children's Health, University of Padova, 35122 Padua, Italy.
  • Wakeling S; The Institute of Cancer Research, London SW7 3RP, UK.
  • Heenen D; Alice's Arc Charity, London EC1V 1AW, UK.
  • Tweddle DA; KickCancer Foundation, 1000 Brussels, Belgium.
  • Merks JHM; Vivo Biobank, Translational & Clinical Research Institute, Newcastle University Centre for Cancer, Newcastle University, Newcastle upon Tyne NE1 7RU, UK.
  • Jenney M; Princess Máxima Center for Pediatric Oncology, 3584 CS Utrecht, The Netherlands.
Cancers (Basel) ; 16(5)2024 Feb 29.
Article en En | MEDLINE | ID: mdl-38473359
ABSTRACT
The Frontline and Relapsed Rhabdomyosarcoma (FaR-RMS) clinical trial is an overarching, multinational study for children and adults with rhabdomyosarcoma (RMS). The trial, developed by the European Soft Tissue Sarcoma Study Group (EpSSG), incorporates multiple different research questions within a multistage design with a focus on (i) novel regimens for poor prognostic subgroups, (ii) optimal duration of maintenance chemotherapy, and (iii) optimal use of radiotherapy for local control and widespread metastatic disease. Additional sub-studies focusing on biological risk stratification, use of imaging modalities, including [18F]FDG PET-CT and diffusion-weighted MRI imaging (DWI) as prognostic markers, and impact of therapy on quality of life are described. This paper forms part of a Special Issue on rhabdomyosarcoma and outlines the study background, rationale for randomisations and sub-studies, design, and plans for utilisation and dissemination of results.
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