Skip Navigation

This Article
Right arrow Full Text Freely available
Right arrow FREE Full Text (PDF) Freely available
Right arrow E-letters: Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when E-letters are posted
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (5)
Right arrowRequest Permissions
Right arrow Disclaimer
Google Scholar
Right arrow Articles by Serin, D.
Right arrow Articles by Flinois, A.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Serin, D.
Right arrow Articles by Flinois, A.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Annals of Oncology 15:1056-1064, 2004
© 2004 European Society for Medical Oncology

‘Parcours de Femme 2001’: a French opinion survey on overall disease and everyday life management in 1870 women presenting with gynecological or breast cancer and their caregivers

Purpose: The aim of the survey ‘Parcours de Femmes 2001’ was to evaluate the overall management and care of women with female cancers and to determine their needs.

Methods: Women with breast or gynecological cancer who had either received at least 3 months of treatment or had completed treatment <1 year before the study were enrolled in this cross-sectional, observational study.

Results: From February to November 2001, 2839 questionnaires were distributed; 1870 were returned (66% response rate), mainly by breast cancer patients (87%). While 92% of women reported having received information at diagnosis, 34% of relapsed patients complained of lack of information concerning their disease and treatment. Only 18% of patients were included in the treatment decision process and 66% of women obtained complementary information from the media, patients and care professionals. Fatigue was the most severe problem quoted (78% of cases) and was poorly managed by caregivers due to diagnostic and treatment difficulties. Problems relating to family and to affective and socio-professional life were poorly identified and remained largely unmanaged.

Conclusions: Information given to female cancer patients must be improved in relapsed patients, particularly regarding the adverse effects of treatment. Psychosocial management requires a more holistic approach through new channels, together with the coordination of existing structures.

D. Serin1,*, J. M. Dilhuydy2, P. Romestaing3, N. Guiochet4, J. Gledhill5, P. Bret6, J. Savary6 and A. Flinois7

1 Institut Sainte-Catherine, Avignon; 2 Institut Bergonié, Bordeaux; 3 Centre Hospitalier Lyon-Sud, Service Radiothérapie, Pierre-Bénite; 4 Centre Hospitalier Princesse Grâce, Service de Radiothérapie, Monaco; 5 Institut Gustave-Roussy, Direction Soins Infirmiers, Villejuif; 6 Bristol-Myers Squibb, Division Oncologie, Rueil-Malmaison; 7 Harris Medical International, Paris, France

*Correspondence to: Dr D. Serin, Institut Sainte-Catherine, Chemin du Lavarin, BP 846, 84086 Avignon cedex 2, France. Tel: +33-4-90-27-62-63; Fax: +33-4-90-89-62-74; Email: danielserin{at}club-internet.fr

Key words: breast cancer, delivery of patient care, gynecological cancer, patient information, supportive care


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?




Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.