| Literature DB >> 29382311 |
Marie Lange1,2,3, Heidi Laviec4, Hélène Castel3,5, Natacha Heutte1,2, Alexandra Leconte2, Isabelle Léger1,3,6,7, Bénédicte Giffard3,8, Aurélie Capel2, Martine Dubois3,5, Bénédicte Clarisse2, Elodie Coquan2,4, Frédéric Di Fiore9,10, Sophie Gouérant9,10, Philippe Bartélémy11, Laure Pierard11, Karim Fizazi12, Florence Joly13,14,15,16.
Abstract
CORRECTION: After publication of the original article [1] the authors found that Table 2 had been formatted incorrectly, meaning that some rows in the Table did not display the correct information. An updated version of Table 2 is included with this Correction. The original article has also been updated.Entities:
Year: 2018 PMID: 29382311 PMCID: PMC5791194 DOI: 10.1186/s12885-017-3764-9
Source DB: PubMed Journal: BMC Cancer ISSN: 1471-2407 Impact factor: 4.430
Used cognitive tests, questionnaires and biological tests
MoCA Montreal Cognitive Assessment, WAIS Wechsler Adult Intelligence Scale, VOSP Visual Object and Space Perception Battery, fNART French National Adult Reading Test, ISI Insomnia Severity Index, VAS Visual Analog Scale, ADL Activities of Daily Living, IADL Instrumental Activities of Daily Living, MNA Mini-Nutritional Assessment
aCognitive assessment will be performed by neuropsychologists
bFor group of interest patients: before the start of the treatment or within 15 days after the start of treatment by abiraterone acetate or enzalutamide
cHad to be ≤3 on the 0–10 pain VAS scale to meet with inclusion pain criteria
dGeriatric assessment will be performed by a study nurse specialized in geriatric
eAdherence evaluation will be performed only in group of interest patients
fAt each time: CBC, platelets, albumin, CRP, prealbumin, iron, ferritin, transferrin, creatinin, sodium, potassium, ALT, AST, GGT, ALP, total bilirubin, TSH, T4, testosterone. At inclusion only: cortisol (at 8 h AM, fasting)
g1 EDTA (5 ml), 1 dry tube with gel (5 ml) and 1 dry tube without gel (5 ml)