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MRD-associated Non-intensive But Non-interruptive Treatment of Ph-negative Acute Lymphoblastic Leukemia Adult Patients

MRD-associated Non-intensive But Non-interruptive Treatment of Ph-negative Acute Lymphoblastic Leukemia Adult Patients

Recruiting
18-55 years
All
Phase N/A

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Overview

Non-intensive But Non-interruptive Treatment based on previously study RALL-2016 of Adult Ph-negative Acute Lymphoblastic Leukemia: 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 remission (CR) with MRD-positive status after 2nd induction receive consolidation 1-3 with venetoclax (56 days), and B-ALL patients in complete remission (CR) with MRD-positive status after 2nd induction receive 1 consolidation with blinatumomab. After that consolidation bone samples are collected and tested for MRD and patients will continue therapy by protocol without HSCT if MRD-negative (by flow cytometry by aberrant immunophenotype in a centralized lab) status was achieved.

Description

  • 7 days prednisolone prephase
    • 8 weeks induction with de-escalation of induction chemotherapy: 3 instead of 4 dauno/vncr pulses,
      1. instead of 2 Cph injections during induction,
      2. instead of 4 ARA-C blocks, distribution of of L-asp injections through all phases
    • After CR achievement T-cell ALL and B-ALL patients are being study MRD (by FCM) MRD-positive patients with T-ALL will receive 1-3 consolidation with venetoclax (400 mg/d), and B-ALL patients will receive1 additional consolidation by blinatumomab
    • Non-interruptive 5 consolidation phases with dose modification according to WBC and platelets count after CR achievement. Rotation of consolidation is permitted
    • 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 allo-HSCT
    • Allo-HSCT is planned only for very high risk patients (11q23 ALL, MRD positivity after target therapy, ETP T-ALL)

Eligibility

Inclusion Criteria:

• age 18-55 years old of patient,

  • Clinical diagnosis of non-treated Ph-negative ALL

Exclusion Criteria:

• age more than 55 years old,

  • Clinical diagnosis of Ph-positive ALL
  • Clinical diagnosis of relapsed/refractory ALL,

Study details
    Precursor Cell Lymphoblastic Leukemia-Lymphoma

NCT06237192

National Research Center for Hematology, Russia

16 February 2024

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