Efficacy and Toxicity of Blinatumomab in the French ATU for Adult BCP-ALL R/R, or With MRD+ (FRENCH-CYTO)

Sponsor
Group for Research in Adult Acute Lymphoblastic Leukemia (Other)
Overall Status
Unknown status
CT.gov ID
NCT03751072
Collaborator
Amgen (Industry)
92
1
6.5
14.1

Study Details

Study Description

Brief Summary

The outcome of young adults (18-60 years) with ALL has been dramatically improved by the use of pediatric-inspired trials. About 60% of these young adult patients will be cured at 5 years. In this context, early evaluation of minimal residual disease (MRD) at complete remission has been shown to be one of the most powerful prognostic factor, but also predictive of the benefit of allogeneic stem cell transplantation (ASCT). Despite this global improvement, about 30% of patients experience a relapse and will be exposed to be refractory to salvage therapy or to early disease escape. In adult ALL, the most important prognostic factors at relapse are : the time from first CR to relapse, the achievement of a second complete remission (CR), and the feasibility of ASCT.

Blinatumomab is a bispecific T-cell engager that recruits T-cell on CD19 positive blast cells and induces anti-leukemic cytotoxicity. In a phase 3 trial in relapse/refractory Philadelphia-negative (Ph-) ALL, 43% of patients achieved a CR or CR with partial hematological recovery (CRh), with the majority of responses occurring within the first cycle. In patients with positive MRD (MRD+) BCP-ALL, blinatumomab resulted in complete MRD response in 78% of patients after one cycle.

Between 2012 and 2016, blinatumomab was available in France for R/R and MRD+ ALL adult patients through the French Compassionate Use Program. About 92 adult ALL were treated at different stages of the disease in 27 centers.

Detailed Description

To evaluate the efficacy of blinatumomab given in the French Compassionate Use Program, in term of overall survival in both R/R (first cohort) and MRD positive (second cohort) patients.

To evaluate the efficacy of blinatumomab given in the French Compassionate Use Program, in term of CR/CRH in R/R patients, To evaluate the efficacy in term of molecular response in both R/R and MRD+ cohorts, To evaluate the efficacy of blinatumomab given in the French Compassionate Use Program, in both Ph+/Ph- ALL patients To evaluate the feasibility and the safety of blinatumomab administration in a multi-center setting.To evaluate the feasibility of allogeneic stem cell transplant after blinatumomab administration in both populations.

Study Design

Study Type:
Observational
Anticipated Enrollment :
92 participants
Observational Model:
Case-Only
Time Perspective:
Retrospective
Official Title:
Efficacy and Toxicity of Blinatumomab in the French Compassionate Use Program (ATU) for Adult Patients With B-cell Precursor Acute Lymphoblastic Leukemia (BCP-ALL) Refractory, in Relapse, or With Positive Minimal Residual Disease.
Actual Study Start Date :
Jul 16, 2018
Anticipated Primary Completion Date :
Nov 30, 2018
Anticipated Study Completion Date :
Jan 30, 2019

Arms and Interventions

Arm Intervention/Treatment
Relapse/Refractory

MRD positive

Outcome Measures

Primary Outcome Measures

  1. Overall Survival in R/R and MRD+ cohorts [6 months]

    Months

Secondary Outcome Measures

  1. Response rates [6 months]

    Percent

  2. Adverse events [6 months]

    Percent

  3. Disease free survival [6 months]

    Months

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:

Patient with Philadelphia-negative or positive (Ph+) ALL in relapse, refractory to salvage therapy, or with MRD positive ALL that received blinatumomab in the French ATU program.,

  • Patient treated in the GRAALL network,

  • Patient who does'nt object to participate in the study

Exclusion Criteria :
  • none

Contacts and Locations

Locations

Site City State Country Postal Code
1 CABANNES-HAMY Aurélie Paris France 75010

Sponsors and Collaborators

  • Group for Research in Adult Acute Lymphoblastic Leukemia
  • Amgen

Investigators

  • Principal Investigator: Nicolas BOISSEL, MD, 142499643

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Group for Research in Adult Acute Lymphoblastic Leukemia
ClinicalTrials.gov Identifier:
NCT03751072
Other Study ID Numbers:
  • FRENCH-CYTO
First Posted:
Nov 23, 2018
Last Update Posted:
Nov 23, 2018
Last Verified:
Nov 1, 2018
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Nov 23, 2018