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Fertility Among Female Survivors of Childhood, Adolescent, and Young Adult Cancer: Protocol for Two Pan-European Studies (PanCareLIFE).
van den Berg, Marleen; van Dijk, Marloes; Byrne, Julianne; Campbell, Helen; Berger, Claire; Borgmann-Staudt, Anja; Calaminus, Gabriele; Dirksen, Uta; Winther, Jeanette F; Fossa, Sophie D; Grabow, Desiree; Grandage, Victoria L; van den Heuvel-Eibrink, Marry M; Kaiser, Melanie; Kepak, Tomas; Kremer, Leontien C; Kruseova, Jarmila; Kuehni, Claudia E; Lambalk, Cornelis B; van Leeuwen, Flora E; Leiper, Alison; Modan-Moses, Dalit; Morsellino, Vera; Spix, Claudia; Kaatsch, Peter; van Dulmen-den Broeder, Eline.
Afiliação
  • van den Berg M; Department of Pediatrics, Amsterdam UMC, Vrije Universiteit, Amsterdam, Netherlands.
  • van Dijk M; Department of Pediatrics, Amsterdam UMC, Vrije Universiteit, Amsterdam, Netherlands.
  • Byrne J; Boyne Research Institute, Drogheda, Ireland.
  • Campbell H; Boyne Research Institute, Drogheda, Ireland.
  • Berger C; Centre Hospitalier Universitaire de Saint-Étienne, Saint-Étienne, France.
  • Borgmann-Staudt A; Division of Oncology and Hematology, Department of Pediatrics, Charité - Universitätsmedizin Berlin, Berlin, Germany.
  • Calaminus G; University Children's Hospital Bonn, University of Bonn Medical School, Bonn, Germany.
  • Dirksen U; Pediatrics III, University Hospital Essen, Essen, Germany.
  • Winther JF; West German Cancer Centre, German Cancer Research Centre, Essen, Germany.
  • Fossa SD; Danish Cancer Society Research Center, Copenhagen, Denmark.
  • Grabow D; Department of Clinical Medicine, Faculty of Health, Aarhus University Hospital, Aarhus, Denmark.
  • Grandage VL; Oslo University Hospital, Oslo, Norway.
  • van den Heuvel-Eibrink MM; German Childhood Cancer Registry, Institute for Medical Biometry, Epidemiology and Informatics, University Medical Center Mainz, Mainz, Germany.
  • Kaiser M; University College London Hospital, London, United Kingdom.
  • Kepak T; Princess Máxima Center for Pediatric Oncology, Utrecht, Netherlands.
  • Kremer LC; Erasmus MC University Medical Center, Rotterdam, Netherlands.
  • Kruseova J; German Childhood Cancer Registry, Institute for Medical Biometry, Epidemiology and Informatics, University Medical Center Mainz, Mainz, Germany.
  • Kuehni CE; International Clinical Research Center of St Anne's University Hospital Brno, Brno, Czech Republic.
  • Lambalk CB; Princess Máxima Center for Pediatric Oncology, Utrecht, Netherlands.
  • van Leeuwen FE; Department of Pediatrics, Amsterdam UMC, University of Amsterdam, Amsterdam, Netherlands.
  • Leiper A; Motol Teaching Hospital, Prague, Czech Republic.
  • Modan-Moses D; Swiss Childhood Cancer Registry, University of Bern, Bern, Switzerland.
  • Morsellino V; Department of Obstetrics and Gynaecology, Amsterdam UMC, Vrije Universiteit, Amsterdam, Netherlands.
  • Spix C; Netherlands Cancer Institute, Amsterdam, Netherlands.
  • Kaatsch P; Great Ormond Street Children's Hospital, London, United Kingdom.
  • van Dulmen-den Broeder E; Edmond and Lily Safra Children's Hospital, Chaim Sheba Medical Center, Tel-Aviv, Israel.
JMIR Res Protoc ; 7(9): e10824, 2018 Sep 14.
Article em En | MEDLINE | ID: mdl-30215599
BACKGROUND: Despite a significant number of studies on female fertility following childhood, adolescent, and young adult (CAYA) cancer, studies establishing precise (dose-related) estimates of treatment-related risks are still scarce. Previous studies have been underpowered, did not include detailed treatment information, or were based on self-report only without any hormonal assessments. More precise assessments of who is at risk for sub- or infertility are needed. OBJECTIVE: The objective of our study is to describe the design and methods of 2 studies on female fertility (a cohort study and a nested case-control study) among female survivors of CAYA cancer performed within the European PanCareLIFE project. METHODS: For the cohort study, which aims to evaluate the overall risk of fertility impairment, as well as the risk for specific subgroups of female CAYA cancer survivors, 13 institutions from 9 countries provide data on fertility impairment. Survivors are defined as being fertility impaired if they meet at least one of 8 different criteria based on self-reported and hormonal data. For the nested case-control study, which aims to identify specific treatment-related risk factors associated with fertility impairment in addition to possible dose-response relationships, cases (fertility impaired survivors) are selected from the cohort study and matched to controls (survivors without fertility impairment) on a 1:2 basis. RESULTS: Of the 10,964 survivors invited for the cohort study, data are available from 6619 survivors, either questionnaire-based only (n=4979), hormonal-based only (n=72), or both (n=1568). For the nested case-control study, a total of 450 cases and 882 controls are identified. CONCLUSIONS: Results of both PanCareLIFE fertility studies will provide detailed insight into the risk of fertility impairment following CAYA cancer and diagnostic- or treatment-related factors associated with an increased risk. This will help clinicians to adequately counsel both girls and young women, who are about to start anticancer treatment, as well as adult female CAYA cancer survivors, concerning future parenthood and to timely refer them for fertility preservation. Ultimately, we aim to empower patients and survivors and improve their quality of life. REGISTERED REPORT IDENTIFIER: RR1-10.2196/10824.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2018 Tipo de documento: Article