Viewing Study NCT05444712



Ignite Creation Date: 2024-05-06 @ 5:50 PM
Last Modification Date: 2024-10-26 @ 2:36 PM
Study NCT ID: NCT05444712
Status: RECRUITING
Last Update Posted: 2023-09-28
First Post: 2022-06-08

Brief Title: Transplantation After Complete Response In Patients With T-cell Lymphoma
Sponsor: Hospices Civils de Lyon
Organization: Hospices Civils de Lyon

Study Overview

Official Title: Transplantation After Complete Response In Patients With T-cell Lymphoma
Status: RECRUITING
Status Verified Date: 2023-09
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: TRANSCRIPT
Brief Summary: Peripheral T-cell lymphoma PTCL encompasses a broad range of post-thymic ie mature sub-entities as defined by the 2017 WHO classification The most common entities are angioimmunoblastic T-cell lymphoma AITL and other Tfh-phenotype PTCL or PTCL not otherwise specified NOS each representing approximately 20 to 25 of mature T- and NKT-cell lymphomas Compared to their B-cell counterparts most PTCL confer dismal prognosis In fact except for anaplastic lymphoma kinase ALK-positive systemic anaplastic large cell lymphoma sALCL 10-year overall survival for patients with PTCL barely exceeds 30 Given the infrequency and the heterogeneity of these malignancies no real consensus on first-line treatment has been established for most PTCL

The place of autologous stem cell transplantation ASCT as a consolidation procedure for patients with PTCL achieving a complete metabolic response after induction is still highly debated ESMO recommendations and recent guidelines from a committee of the American Society for Blood and Marrow Transplantation currently propose ASCT as first-line therapy for transplant-eligible patients for all patients reaching at least a partial response PR after induction NCCN guidelines version 22017 recommend ASCT or observation in case of metabolic CR but salvage regimen in case of residual disease after induction
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None