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Clinical Trial Summary

The co-primary objectives will be to assess the safety and quality of life under treatment.


Clinical Trial Description

The co-primary objectives will be to assess the safety and quality of life under treatment. Secondary objectives will be evaluations of geriatric data modifications under treatment, efficacy (progression-free survival and overall survival), correlation between toxicity and efficacy, and comparison of the safety profiles between various immunotherapy regimens.

Another secondary objective will be the comparison between patients and clinicians symptom reporting. The investigators will also perform a pharmacokinetics analysis on PD1-monoclonal antibodies to improve the understanding of PD-1 inhibitors pharmacokinetics for the elderly population.

Finally, toxicity and efficacy will be compared to immunological parameters such as the description of tumor infiltrating lymphocytes, markers of immunosenescence and inflammation. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03673332
Study type Interventional
Source Institut Paoli-Calmettes
Contact Dominique GENRE, MD
Phone 33 (0)4 91 22 37 78
Email DRCI.UP@ipc.unicancer.fr
Status Recruiting
Phase Phase 4
Start date August 9, 2019
Completion date December 31, 2021

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