The study will evaluate the detection of tumor-antigen specific immune cells in cancer patients in whom the role of the immune system is suspected.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
OTHER
Masking
NONE
Enrollment
300
lymphapheresis before and during treatment, blood sample in CellSave® tubes (15mL) will be taken at baseline and three weeks, and EDTA tubes (15mL) will be taken at baseline, 3 weeks after treatment start and at progression
lymphapheresis will be performed between 8 weeks and 18 months after the start of treatment
Institut Curie
Paris, France
RECRUITINGInstitut Curie
Saint-Cloud, France
RECRUITINGEvaluation of the presence of tumor-antigen specific T cells for Cohorts A
Presence of tumor-antigen specific T cells using multiplex tetramers and ELISPOTs.
Time frame: before treatment
Evaluation of the presence of tumor-antigen specific T cells for Cohorts A
Presence of tumor-antigen specific T cells using multiplex tetramers and ELISPOTs.
Time frame: During treatment
Evaluation of the presence of tumor-antigen specific T cells for Cohorts A
Presence of tumor-antigen specific T cells using multiplex tetramers and ELISPOTs.
Time frame: at baseline
Evaluation of the presence of tumor-antigen specific T cells for Cohorts A
Presence of tumor-antigen specific T cells using multiplex tetramers and ELISPOTs.
Time frame: 3 weeks after treatment start
Evaluation of the presence of tumor-antigen specific T cells for Cohorts A
Presence of tumor-antigen specific T cells using multiplex tetramers and ELISPOTs.
Time frame: at progression (up to 100 weeks)
Evaluation of the presence of tumor-antigen specific T cells for Cohorts B
Presence of tumor-antigen specific T cells using multiplex tetramers and ELISPOTs.
Time frame: between 8 weeks and 18 months after the start of treatment
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