The aim of the present study is to evaluate the clinical social work in onc
ology. We present a series of 137 men and 63 women treated for cancer (mean
age: 57 y; 20-90) who were addressed (65%) or came spontaneously (35%) for
a first social consultation; 45 consultations concerned the family at the
day of death of the patient. The collected data (expressed requests, evalua
ted real difficulties, orientations of the social work, necessity of networ
k) are correlated with the medical data and the time between diagnosis and
social consultation. The social intervention is often brief (95%) and focus
ed (66%). A medical and social network is used in 70% of cases. The adminis
tration and psychosocial problems predominate with an important discordance
between the requests and the evaluated difficulties. The metastatic status
increase psychosocial, legal difficulties and problems of the organisation
of home-care. The delay of the social consultation has great influence upo
n the legal difficulties. The family's difficulties, after the patient's de
ath are administrative (93.3%), psychosocial (84.4%) and legal (68.9%). Cli
nical social work is part of the global management of patients and their fa
milies; its quality has direct implication on their daily life during and a
fter treatment.