CHU de Saint-Etienne
Saint-Etienne, 42055, France
Location status: Recruiting
NCT Number: NCT04517656
Chemotherapy or targeted therapy are usually used to treat hematological pathologies. Despite of medical improvement, some of these pathologies present drug resistances, or high risk of relapse. Hematopoietic stem cell (HSC) transplantation remain the gold standard of consolidation, to maintain a durable response. In this situation, allograft with hematopoietic stem cells donor aims at producing Graft-versus-Tumor effect, by producing a new immune system, reproducing anti-tumoral immunity.
However, all hemopathies do not have the same sensibility. Nowadays, mechanisms underlying this phenomenon remain poorly understood.
Indeed, few data precisely document the expression of immunological checkpoints and other biomarkers in the context of allogeneic HSC transplantation, particularly their impact on post-transplant outcome.
Interested in participating?
Request Info18 year and older
All sexes
Interventional
Not applicable
Saint-Etienne, 42055, France
Location status: Recruiting
Chemotherapy or targeted therapy are usually used to treat hematological pathologies. Despite of medical improvement, some of these pathologies present drug resistances, or high risk of relapse. Hematopoietic stem cell (HSC) transplantation remain the gold standard of consolidation, to maintain a durable response. In this situation, allograft with hematopoietic stem cells donor aims at producing Graft-versus-Tumor effect, by producing a new immune system, reproducing anti-tumoral immunity.
However, all hemopathies do not have the same sensibility. Nowadays, mechanisms underlying this phenomenon remain poorly understood.
Indeed, few data precisely document the expression of immunological checkpoints and other biomarkers in the context of allogeneic HSC transplantation, particularly their impact on post-transplant outcome. Therefore, we want to systematically study the expression profile of different biomarkers during allogeneic transplantation, in order to establish a correlation between these expression patterns and post-transplant outcome. Ultimately, this research will enable to (i) have tools to predict the post-transplant response and (ii) define whether a targeted therapy could be beneficial or be contraindicated for adequate patient management.
Patients will be selected for the study once they meet all the inclusion criteria. The study will be proposed to them during the pre-allogeneic consultation as part of their usual care. This study does not modify the treatment or the usual management of patients according to the current practice of pre- and post-transplant management. Clinically, it consists of building up a relevant biological collection.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
A peripheral blood sample will be taken and will include 2 EDTA tubes of 5 mL, for a total volume of 10 mL:
Time frame: 12 months
Expression level of Programmed death-ligand (PD) plasmatic biomarkers will be quantified
Time frame: 12 months
Expression level of ST2 (suppression of tumourigenicity 2) plasmatic biomarkers will be quantified
Time frame: 12 months
Expression level of Reg3 (regenerating islet-derived 3-alpha) plasmatic biomarkers will be quantified
Time frame: 12 months
Expression level of Elafin plasmatic biomarkers will be quantified
Interested in participating?
Request InfoCentre Hospitalier Universitaire de Saint Etienne
Other
Biomarkers Impact Evaluation on the Post-transplant Immune Response After Allografting of Hematopoietic Stem Cells: MENTALO Study
Acronym: MENTALO
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT04390126
AMD and Macular Edema, Arteritis
Dijon, France
View Trial DetailsNCT03965429
Malignant Hemopathy
Marseille, Bouches-du Rhône, France
View Trial DetailsNCT01574235
Agranulocytosis, Chemotherapy-Induced Febrile Neutropenia
Colmar, Alsace, France
View Trial Details