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De-escalated Treatment Approach for Adult Ph-negative Acute Lymphoblastic Leukemia (ALL)

Primary Purpose

Precursor Cell Lymphoblastic Leukemia-Lymphoma

Status
Unknown status
Phase
Not Applicable
Locations
Russian Federation
Study Type
Interventional
Intervention
Autologous HSCT
Sponsored by
National Research Center for Hematology, Russia
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Precursor Cell Lymphoblastic Leukemia-Lymphoma

Eligibility Criteria

18 Years - 55 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • age 18-55 yy, newly diagnosed non-treated Ph-negative ALL

Exclusion Criteria:

  • age > 55 yy, Ph-positivity, relapsed|refractory ALL, pretreated ALL

Sites / Locations

  • National Research Center for HematologyRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Experimental

Arm Label

no Auto-HSCT

Auto-HSCT

Arm Description

After completing prolonged consolidation T-cell ALL patients will continue with 2 years maintenance

After completing prolonged consolidation T-cell ALL patients will get autologous HSCT followed by 2 years maintenance

Outcomes

Primary Outcome Measures

Disease-free survival
Impact of autologous HSCT on DFS in T-cell ALL patients

Secondary Outcome Measures

MRD-negativity after consolidation
Minimal Residual Disease clearance on non-intensive but non-interruptive treatment
Overall survival
Impact of de-escalated approach on OS

Full Information

First Posted
March 6, 2018
Last Updated
March 12, 2018
Sponsor
National Research Center for Hematology, Russia
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1. Study Identification

Unique Protocol Identification Number
NCT03462095
Brief Title
De-escalated Treatment Approach for Adult Ph-negative Acute Lymphoblastic Leukemia (ALL)
Official Title
Non-intensive But Non-interruptive Treatment of Adult Ph-negative Acute Lymphoblastic Leukemia With Randomization for Maintenance or Autologous Hematopoietic Stem Cell Transplantation (HSCT) Followed by Maintenance in T-cell ALL Patients
Study Type
Interventional

2. Study Status

Record Verification Date
March 2018
Overall Recruitment Status
Unknown status
Study Start Date
January 2017 (Actual)
Primary Completion Date
December 1, 2019 (Anticipated)
Study Completion Date
December 1, 2022 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
National Research Center for Hematology, Russia

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
No high-dose methotrexate (MTX) and high-dose cytarabine (ARA-C) consolidation blocks, L-asparaginaseis scheduled for 1 year of treatment, 21 intrathecal injections through the whole treament, T-ALL patients in complete remossion (CR) after the informed consent are randomized to: auto-HSCT vs no auto-HSCT, - with the similar further maintenance. Stem cell harvest is performed after the 3rd consolidation by G-SCF disregarding minimal residual disease (MRD) level. Auto-HSCT is planned after the 5th consolidation phase. All primary bone samples are collected and tested for cytogenetics and molecular markers, all included patients are monitored by flow cytometry by aberrant immunophenotype in a centralized lab.
Detailed Description
7 days prednisolone prephase 8 weeks induction with de-escalation of induction chemotherapy: 3 instead of 4 dauno/vncr pulses, instead of 2 Cph injections during induction, instead of 4 ARA-C blocks, distribution of of L-asp injections through all phases After CR achievement T-cell ALL patients are being randomized to auto-HSCT vs no auto-HSCT Non-interruptive 5 consolidation phases with dose modification according to WBC and platelets count after CR achievement. Rotation of consolidation is permitted After the 3rd consolidation stem cells harvesting is carried out for T-cell ALL patients randomized to auto-HSCT Auto-HSCT after the 5th consolidation phase with non-myeloablative CEAM conditioning 2 years maintenance for all patients 21 TIT through the whole treatment with higher intensity during induction|consolidation Centralized MRD monitoring at +70 d, + 133 d, + 190 days; before and after auto-HSCT Allo-HSCT is planned only for very high risk patients (11q23 ALL, MRD positivity at day +190)

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Precursor Cell Lymphoblastic Leukemia-Lymphoma

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Factorial Assignment
Masking
Investigator
Allocation
Randomized
Enrollment
350 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
no Auto-HSCT
Arm Type
No Intervention
Arm Description
After completing prolonged consolidation T-cell ALL patients will continue with 2 years maintenance
Arm Title
Auto-HSCT
Arm Type
Experimental
Arm Description
After completing prolonged consolidation T-cell ALL patients will get autologous HSCT followed by 2 years maintenance
Intervention Type
Procedure
Intervention Name(s)
Autologous HSCT
Intervention Description
After the 3rd consolidation, T-cell ALL patients, randomized to auto-HSCT will be mobilised by G-SCF and harvested disregarding MRD-status. After completing the 5th consolidation T-ALL patients will be transplanted after non-myeloablative CEAM (CCNU, Ethoposide, ARA-C, Melphalan) conditioning, and after reconstitution will continue 2-years maintenance
Primary Outcome Measure Information:
Title
Disease-free survival
Description
Impact of autologous HSCT on DFS in T-cell ALL patients
Time Frame
5-years
Secondary Outcome Measure Information:
Title
MRD-negativity after consolidation
Description
Minimal Residual Disease clearance on non-intensive but non-interruptive treatment
Time Frame
6 months
Title
Overall survival
Description
Impact of de-escalated approach on OS
Time Frame
5-years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
55 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: age 18-55 yy, newly diagnosed non-treated Ph-negative ALL Exclusion Criteria: age > 55 yy, Ph-positivity, relapsed|refractory ALL, pretreated ALL
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Elena N Parovichnikova, MD,PhD
Phone
+79161252623
Email
elenap@blood.ru
First Name & Middle Initial & Last Name or Official Title & Degree
Olga A Gavrilina, M.D.
Email
dr.gavrilina@mail.ru
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Valeriy V Savchenko, Academician
Organizational Affiliation
National Research Center for hematology, Moscow, Russia
Official's Role
Study Director
Facility Information:
Facility Name
National Research Center for Hematology
City
Moscow
ZIP/Postal Code
125167
Country
Russian Federation
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Elena N Parovichnikova, MD PhD
Phone
+7(495)6124313
Email
elenap@blood.ru

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
Each participating site has its on-line access to WEB-data base
IPD Sharing Time Frame
Once a year
IPD Sharing Access Criteria
phone-call to coodinating center

Learn more about this trial

De-escalated Treatment Approach for Adult Ph-negative Acute Lymphoblastic Leukemia (ALL)

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