International Study for Treatment of High Risk Childhood Relapsed ALL 2010

Last updated: February 8, 2024
Sponsor: Charite University, Berlin, Germany
Overall Status: Active - Recruiting

Phase

2

Condition

Leukemia (Pediatric)

Treatment

Bortezomib

Clinical Study ID

NCT03590171
IntReALL HR 2010
  • Ages < 17
  • All Genders

Study Summary

The main goal of this study is to improve the outcome of children and adolescents with acute lymphoblastic leukemia with high risk first relapse by optimization of treatment strategies within a large international trial and the integration of new agents.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Morphologically confirmed diagnosis of 1st relapsed precursor B-cell or T-cell ALL
  • Children less than 18 years of age at date of inclusion into the study
  • Meeting HR criteria any BM relapse, early/very early isolated BM relapse, very earlyisolated/combined extramedullary relapse)
  • Patient enrolled in a participating centre
  • Written informed consent
  • Start of treatment falling into the study period
  • No participation in other clinical trials 30 day prior to study enrolment thatinterfere with this protocol, except trials for primary ALL

Exclusion

Exclusion Criteria:

  • Breakpoint cluster region-Abelson (BCR-ABL)/ t(9;22) positive ALL
  • Pregnancy or positive pregnancy test (urine sample positive for β-humanechoriongonadotropin (HCG) > 10 U/l)
  • Sexually active adolescents not willing to use highly effective contraceptive method (pearl index <1) until 12 months after end of anti-leukemic therapy
  • Breast feeding
  • Relapse post allogeneic stem-cell transplantation
  • Neuropathy > II°
  • The whole protocol or essential parts are declined either by patient himself/herselfor the respective legal guardian
  • Objection to the study participation by a minor patient, able to object
  • Any patient being dependent on the investigator
  • No consent is given for saving and propagation of pseudonymized medical data for studyreasons
  • Severe concomitant disease that does not allow treatment according to the protocol atthe investigator's discretion (e.g. malformation syndromes, cardiac malformations,metabolic disorders)
  • Subjects unwilling or unable to comply with the study procedures
  • Subjects who are legally detained in an official institute

Study Design

Total Participants: 250
Treatment Group(s): 1
Primary Treatment: Bortezomib
Phase: 2
Study Start date:
September 01, 2017
Estimated Completion Date:
December 31, 2027

Study Description

Though survival of children with acute lymphoblastic leukemia (ALL) has considerably improved over the past few decades, relapsed ALL remains a leading cause of mortality in children with cancer. Risk has been defined by the International (I) Berlin, Frankfurt, Münster (BFM) Study Group (SG) based on duration of first remission, immunophenotype of malignant clone, and site of relapse. Patients classified as high risk (HR) by these criteria have poor response rates to standard induction therapy, high rates of subsequent relapse and require an allogeneic hematopoetic stem cell transplantation (allo-HSCT) for consolidation of 2nd remission. Over the last decade members of the I-BFM-SG have investigated the use of different combinations of conventional cytotoxic agents. Even with allo-HSCT, none of these approaches have improved outcome above 40%. Therefore, for HR patients there is a need to investigate the curative potential of new agents combined with systemic therapy. The proteasome inhibitor bortezomib has shown synergistic activity with acceptable toxicity when combined with corticosteroids, anthracyclines and alkylating agents in adult patients with cancer as well as with dexamethasone, doxorubicin, vincristine and polyethylene glycol (PEG) asparaginase in children with refractory or relapsed ALL. In the I-BFM-SG International Study for Treatment of High Risk Childhood Relapsed ALL (IntReALL) HR 2010 study, the potential of Bortezomib combined with a modified ALL relapse protocol 3 (R3) backbone as induction regimen for HR patients to improve complete 2nd remission (CR2) rates will be investigated in a randomized phase II design. Induction is followed by conventional intensive consolidation. After termination of the trial patients may be subjected to an investigational window, before all of them receive allo-HSCT.

Connect with a study center

  • Australian & New Zealand Childhood Hematology & Oncology Group

    Clayton, Victoria 3168
    Australia

    Active - Recruiting

  • St. Anna Kinderkrebsforschung, CCRI

    Vienna, 1090
    Austria

    Active - Recruiting

  • Hòpital Universitaire des Enfants Reine Fabiola

    Bruxelles, 1020
    Belgium

    Active - Recruiting

  • University Hospital Motol

    Prague,
    Czechia

    Active - Recruiting

  • Copenhagen University Hospital (Rigshospitalet)

    Copenhagen, 2100
    Denmark

    Site Not Available

  • Turku University Central Hospital

    Turku, SF-20520
    Finland

    Active - Recruiting

  • CHU Nice

    Nice,
    France

    Active - Recruiting

  • Tel Aviv Sourasky Medical Centre

    Tel Aviv, 64239
    Israel

    Active - Recruiting

  • Ospedale Pediatrico Bambino Gesù

    Roma, 00165
    Italy

    Active - Recruiting

  • St.Lukes International Hospital

    Tokyo,
    Japan

    Site Not Available

  • Prinses Máxima Centrum, Lundlaan

    Utrecht,
    Netherlands

    Active - Recruiting

  • Oslo University Hospital

    Oslo, 0027
    Norway

    Site Not Available

  • Dpt. SCT and Hematology/Oncology University Wroclaw

    Wroclaw, 50354
    Poland

    Active - Recruiting

  • Instituto Português de Oncologia de Lisboa

    Lisboa,
    Portugal

    Site Not Available

  • University Hospital Stockholm

    Stockholm, 17176
    Sweden

    Site Not Available

  • Royal Manchester Children's Hospital

    Manchester, M13 9WL
    United Kingdom

    Site Not Available

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