About this trial

This study aims to investigate the occurrence of cancer and adjuvant therapy-related cognitive impairment in patients with both NSCLC and SCLC. The primary endpoint measure will be the presence of cognitive impairment during the first year after enrollment through the administration of a comprehensive neuropsychological assessment.

Eligibility criteria

Qualifiers

Small-cell and non-small-cell lung cancer (stage I, II, III, IV)

Age ≥ 18 years

Patients able to speak and read the local language(s) fluently

Acceptance and signature of informed consent

Disqualifiers

Age ≥ 70

Presence of brain metastases

Patients with concomitant neurological or psychiatric disorders.

Patients undergoing brain radiotherapy

Trial design

Treatments tested in this trial

  • Not listed

Trial groups

200 Participants
are grouped into 1 trial group

Locations

1
Istituto Europeo di Oncologia20141, Milan Italy

Sponsors and collaborators

European Institute of Oncology

Lead sponsor