End of life and clinical research in pediatric oncology;Fin de vie de l'enfant et recherche clinique en cancérologie pédiatrique

Archives de Pediatrie

Volumn 14, Issue 3, 2007, Pages 274-278

  Davous, D ^a   Doz, F ^a   Heard, M ^a  

^a SAINT LOUIS HOSPITAL   (France)

Author keywords

Clinical research; Clinical trials; Ethics; Medical oncology; Pediatrics; phase I

Indexed keywords

CHILDHOOD CANCER; CLINICAL RESEARCH; CRITERION VARIABLE; DISEASE CONTROL; ETHICAL DECISION MAKING; EXPLORATORY RESEARCH; HEALTH CARE PERSONNEL; HUMAN; PARENTAL NOTIFICATION; PATIENT INFORMATION; PHILOSOPHY; PRACTICE GUIDELINE; QUALITY OF LIFE; SELF CONCEPT; SHORT SURVEY; TERMINAL CARE; TIME MANAGEMENT; CHILD; ETHICS; NEOPLASM; PHASE 1 CLINICAL TRIAL; REVIEW; TERMINALLY ILL PATIENT;

CHILD; CLINICAL TRIALS, PHASE I; HUMANS; NEOPLASMS; TERMINALLY ILL;

EID: 33847413124     PISSN: 0929693X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.arcped.2006.11.020     Document Type: Short Survey

References (15)

1. Mon enfant et la recherche en cancérologie, livret d'information et d'aide à la décision à l'usage des parents. Groupe « Parents et soignants face à l'éthique en pédiatrie ». Juin 2005 : forum.espace-ethique@sls.aphp.fr.
2. Thouvenel C., Geny M.S., Demirdjian S., et al. Autorisation de mise sur le marché et information pédiatrique pour les médicaments de chimiothérapie des cancers : état des lieux et propositions. Arch. Pediatr. 9 (2002) 685-693
3. Smith M., Bernstein M., Bleyer W.A., et al. Conduct of phase I trials in children with cancer. J. Clin. Oncol. 16 (1998) 966-978
4. Oberman M., and Frader J. Dying children and medical research : access to clinical trials as benefit and burden. Am. J. Law Med. 29 (2003) 310-317
5. Horng S., Emanuel E.J., Wilfond B., et al. Descriptions of benefits and risks in consent forms for phase 1 oncology trials. N. Engl. J. Med. 347 (2002) 2134-2140
6. Estlin E.J., and Ablett S. Practicalities and ethics of running clinical trials in paediatric oncology - the UK experience. Eur. J. Cancer 37 (2001) 1394-1398 (discussion 1399-401)
7. Deatrick A., Angst D.B., and Moore C. Parents'views of their children's participation in phase I oncology clinical trials. J. Pediatr. Oncol. Nurs. 19 (2002) 114-121
8. Humbert N, editor. Les soins palliatifs pédiatriques. Montréal, Québec : éditions de l'hôpital Sainte-Justine, collection Intervenir; 2004. (Diffusion en France : Casteilla, Tél. : 01 30 14 19 30 et casteilla@wanadoo.fr).
9. Ulrich C.M., Grady C., and Wendler D. Palliative care: a supportive adjunct to pediatric phase I clinical trials for anticancer agents?. Pediatrics 114 (2004) 852-855
10. Spinetta J.J., Masera G., Jankovic M., et al. Valid informed consent and participative decision-making in children with cancer and their parents: a report of the SIOP Working Committee on psychosocial issues in pediatric oncology. Med. Pediatr. Oncol. 40 (2003) 244-246
11. ° 2004-806 du 9 août 2004, relative à la politique de santé publique. J. Officiel de la République Française 11 (2004) 31-40
12. Chappuy H., Doz F., Blanche S., et al. Parental consent in pediatric clinical research. Arch. Dis. Child. 91 (2006) 112-116
13. Bercovitz A., Limagne M.P., and Sentilhes-Monkam A. Retour au domicile d'un enfant en fin de vie. Arch. Pediatr. 8 (2001) 1175-1177
14. Kreicbergs U., Valdimarsdóttir U., Onelöv E., et al. Talking about death with children who have severe malignant disease. N. Engl. J. Med. 351 (2004) 1175-1186
15. Ernoult A. Le point de vue des parents. In: Humbert N. (Ed). Les soins palliatifs pédiatriques (2004), éditions de l'hôpital Sainte-Justine, collection Intervenir, Montréal, Québec 487