Clinical Trials Logo

Clinical Trial Summary

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.


Clinical Trial Description

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. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04517656
Study type Interventional
Source Centre Hospitalier Universitaire de Saint Etienne
Contact Jérôme Cornillon, MD
Phone 477917089
Email elisabeth.daguenet@chu-st-etienne.fr
Status Recruiting
Phase N/A
Start date May 25, 2022
Completion date September 30, 2025

See also
  Status Clinical Trial Phase
Completed NCT01574235 - Nivestim® (Filgrastim) Tolerance in Patients Treated by Toxic Chemotherapeutic Agents N/A
Recruiting NCT03965429 - Immunological Follow-up After Allogeneic Hematopoietic Stem Cell Transplantation
Terminated NCT02999152 - Validation of Radio-induced Damage Biomarkers N/A
Terminated NCT00190463 - Comparison of 2 Antifungal Treatment (Empirical Versus Pre-Empirical) Strategies in Prolonged Neutropenia Phase 4
Active, not recruiting NCT04390126 - COVID-19 Related Lockdown Effects On Chronic Diseases