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PROspective Master-protocol for Evaluation of Systemic THErapeutics in Elderly
The objective of the study is to prospectively generate real-life data in patients aged ≥70 years treated in first line for a thoracic tumor (Non-Small-Cell Lung Carcinoma) according to best standard of care as defined by the European Society for Medical Oncology (ESMO). This cohort will aim to: * characterize participants in terms of geriatrics, biology and carcinology * describe the treatment modalities by stage, as well as the results in terms of efficacy, safety and impact on quality of life. At the same time, exploratory sub-cohorts will be identified including participants treated uniformly with the same molecule, and/or the same innovative strategy. Participants will be followed in accordance with investigator's usual clinical practice at the corresponding site. They will be asked to: * visit the clinic as per physician's request for checkups and tests for assessing general condition and clinical efficacy and tolerance of current treatment. * perform the necessary regular para-clinical examinations (lab testing, imaging, re-biopsy). * provide blood samples for bio-bank repository * perform assessments specific to older adults * answer three quality of life questionnaires
Age
70 - No limit years
Sex
ALL
Healthy Volunteers
No
CH du Pays d Aix
Aix-en-Provence, France
Hôpital Henri Duffaut
Avignon, France
Institut du Cancer d'Avignon
Avignon, France
CH Bastia
Bastia, France
Oncologie Thoracique Hôpital Morvan
Brest, France
Pneumologie Centre François Baclesse
Caen, France
CH Métropole-Savoie
Chambéry, France
Centre Hospitalier du Cotentin
Cherbourg, France
CHU Hôpital Montpied
Clermont-Ferrand, France
Pneumologie Hospices Civils de Colmar
Colmar, France
Start Date
September 26, 2024
Primary Completion Date
August 31, 2026
Completion Date
August 31, 2028
Last Updated
December 16, 2025
500
ESTIMATED participants
Bio-bank repository
GENETIC
Quality of Life (QoL)
OTHER
G-Code
PROCEDURE
Lead Sponsor
GFPC Investigation
NCT06066138
NCT07190248
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT07336732