Clinical Research Directory

Inclusion Criteria: * Male or female ≥ 18 years at the day of consenting to the study; * Confirmed diagnosis of any type of solid or haematology tumours, with or without Current oncological treatment, such as chemotherapy, immunotherapy, targeted therapy, etc; * Unscheduled admission in a French Regional Comprehensive Anti-Cancer Centre due to an acute, unpredictable, intercurrent event related to cancer, its therapies or a comorbidity; * Patient for whom disease is considered as not curable; * PALLIA-10 Score \> 3/10; * Willingness and ability to comply with the study requirements; * Signed and dated informed consent indicating that the patient has been informed of all the aspects of the trial prior to enrolment; * Patient must be covered by a medical insurance. Exclusion Criteria: * Patient without consciousness, unable to provide a written informed consent (context of emergency); * Patient treated with a curative intent; * Previous randomization in this clinical study; * Patients already followed-up by a palliative care team; * Life expectancy shorter than 1 month, as per the emergency units' staff judgement. * Any medical or psychosocial condition that would compromise the patient's compliance to the study visits or would likely interfere with the completion of Patient-Reported Outcomes. * Patients under tutorship or curatorship.