CClinicalTrials.gg
CompletedNCT01802814Updated Feb 9, 2024

International Study for Treatment of Standard Risk Childhood Relapsed ALL 2010

A Phase 3 interventional study of SR-A + Epratuzumab and SR-B + Epratuzumab in Acute Lymphoblastic Leukemia (ALL), sponsored by Charite University, Berlin, Germany. Completed at 17 sites in 17 countries. Open to participants aged 1 Day to 17 Years. Per ClinicalTrials.gov, last updated 2024-02-09.

Sponsored by Charite University, Berlin, Germany · Phase 3, Interventional, and Treatment

Phase
Phase 3
Study type
Interventional
Enrollment
700
Allocation
Randomized
Ages
1 Day to 17 Years
Sex
All
01

Study summary

The main goal of this study is to improve the outcome of children and adolescents with standard risk (SR) first relapsed acute lymphoblastic leukemia. Furthermore, goal is to set up a large international study group platform allowing for optimization of standard treatment strategies and integration of new agents.

Read the detailed description

ALL is the most frequent malignancy in childhood and has favourable event-free and overall survival rates. About 15% of patients suffer relapse. At relapse prognosis is much inferior (about 50% survival) leukemic clones exhibit much more resistance to conventional chemotherapy. Patients with relapse require treatment intensification and different therapeutic strategies. At relapse, new targeted agents can provide the chance for better cure rates and need to be investigated in prospective controlled trials before they may be even eligible for frontline treatment strategies.

The IntReALL SR 2010 trial is designed to achieve 2 major aims: Establishment of the best available standard chemotherapy treatment. This is addressed with the randomization of the 2 best developed strategies for treatment of childhood relapsed ALL, the German ALL-REZ BFM 2002 Protocol with the Protocol II IDA arm, and the British ALL-R3 protocol with the mitoxantrone arm. This randomization allows confirming the feasibility of both protocols in a large variety of different countries and study groups with different frontline therapy strategies. As result from this trial a common standard chemotherapy for childhood relapsed ALL will be developed which can serve as backbone for investigation of the most attractive targeted new agents.

The 2nd aim is the investigation of the efficacy and tolerability of the humanized CD22 directed monoclonal antibody Epratuzumab, manufactured and provided by the company Immunomedics, US. The drug will be randomly added to the respective consolidation chemotherapy, using EFS as primary endpoint. Epratuzumab has been developed in adult rheumatology indications and in B-cell malignancies. A phase I and early phase II combination trial in childhood relapse ALL has been conducted and published by the Children's Oncology Group (COG), and results of an extended phase II trial have been recently presented at the ASH meeting (12/2011). The drug showed a very favourable safety profile as single drug and in combination with multidrug chemotherapy. Activity was moderate, the recent trial showed a significantly better elimination of minimal residual disease (MRD) in patients achieving a 2nd complete remission. This finding supports the strategy to use Epratuzumab in combination with consolidation chemotherapy after induction in patients having reduced the leukemia burden in the bone marrow to at least below 25%, most of them will be in 2nd complete remission. Epratuzumab will be given weekly at the established dose. Pharmacokinetics will be investigated in a reduced number of patients. The further treatment will be conventional intensive chemotherapy and maintenance therapy in patients with good MRD response after induction, or with allogeneic stem-cell transplantation (SCT) in those with insufficient MRD response. SCT will be considered as standard treatment element and will not lead to censoring of the patients of considered as endpoint. Epratuzumab is not licensed so far and the trial may add to the approval process in case.

Scientific advice for the trial has been requested at the FDA and the EMA. Both institutions have responded supportively. Concerns and recommendations of FDA and EMA have been addressed in the protocol and the corresponding statistical analysis plan.

The IntReALL SR 2010 trial will be financed within the FP7 project IntReALL 2010 supported by the European Commission. Within the project next to the SR trial a strategy for high Risk (HR) patients will be addressed, the establishment of harmonized diagnostic procedures, an international tumour bank and a comprehensive biologic/scientific programme will be set up, a web-based Good Clinical Practice (GCP) conform database will be established, a comprehensive statistical strategy for both trials are established, and drug development in this indication will be promoted and organized from side of the disease experts in cooperation with the established academic structures ITCC (Innovative Therapies for Children with Cancer), the ENCCA project (European Network for Cancer in Children and Adolescents) and SIOPe (International Society for Pediatric Oncology Europe), the central authorities (EMA, FDA) and Industry. Parent organisation and former patients are integrated into and accompany the process.

Main aims of the IntReALL FP7 project are to establish a therapeutic platform for children with relapsed ALL in Europe and beyond and to give them access to the most promising new agents under academic control and free from commercial interests.

Randomized evidence for efficacy and tolerability of new drugs are demanded by competent authorities. These trials are conducted beyond the mostly palliative patient group eligible for phase I/II trials in curative indications. Treatment protocols for with curative indications need to be conducted in the best interests of the patients, ideally with an academic sponsor. The design should be driven by medical and scientific evidence and not by commercial interests as is the case in industry sponsored trials. This concept was acknowledged by the European Commission selecting the project for funding from many other powerful applications.

02

Conditions studied

  • Acute Lymphoblastic Leukemia (ALL)

Keywords

  • ALL
03

In context

Precursor Cell Lymphoblastic Leukemia-Lymphoma

2,061 studies on the registry are indexed under Precursor Cell Lymphoblastic Leukemia-Lymphoma; 490 are open to participants now.

This study's enrollment of 700 is above the median of 40 across 1,653 interventional studies indexed under Precursor Cell Lymphoblastic Leukemia-Lymphoma.

Browse Precursor Cell Lymphoblastic Leukemia-Lymphoma studies →

Lead sponsor

Charite University, Berlin, Germany is the lead sponsor of 836 studies on the registry; 129 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
1 Day to 17 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Morphologically confirmed diagnosis of 1st relapsed precursor B-cell or T-cell ALL
  • Children less than 18 years of age at inclusion
  • Meeting SR criteria: late isolated or late/early combined B-cell precursor (BCP) bone marrow (BM) relapse, any late/early isolated 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 days prior to study enrolment that interfere with this protocol, except trials for primary ALL Inclusion criteria specific for the epratuzumab randomization
  • Precursor B-cell immunophenotype. A specific CD22 expression level is not required
  • M1 or M2 status of the bone marrow after induction

Exclusion criteria

Exclusion Criteria:

  • BCR-ABL / t(9;22) positive ALL
  • Pregnancy or positive pregnancy test (urine sample positive for β-HCG > 10 U/l)
  • Sexually active adolescents not willing to use highly effective contraceptive method (pearl index \<1) until 2 years after end of antileukemic therapy
  • Breast feeding
  • Relapse post allogeneic stem-cell transplantation
  • The whole protocol or essential parts are declined either by patient himself/herself or the respective legal guardian
  • No consent is given for saving and propagation of pseudonymized medical data for study reasons
  • Severe concomitant disease that does not allow treatment according to the protocol at the investigator's discretion (e.g. malformation syndromes, cardiac malformations, metabolic disorders)
  • Karnovsky / Lansky score \< 50%
  • Subjects unwilling or unable to comply with the study procedures
  • Subjects who are legally detained in an official institute
05

Study design

Phase
Phase 3
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
700 participants (actual)

Study arms

  • No intervention
    SR-A

    Patients randomized to the SR-A Arm receive induction, consolidation and maintenance therapy according to a modified protocol ALL-REZ BFM 2002 with Protocol II-IDA as 1st consolidation element. In this arm patients are randomized not to receive epratuzumab.This randomization has been stopped pre-term on 1.2.2019 since the investigational product is not provided anymore by the manufacturer.

  • Active comparator
    SR-A + Epratuzumab

    Patients randomized to the SR-A Arm receive induction, consolidation and maintenance therapy according to a modified protocol ALL-REZ BFM 2002 with Protocol II-IDA as 1st consolidation element. In this arm patients are randomized to receive epratuzumab. This randomization has been stopped pre-term on 1.2.2019 since the investigational product is not provided anymore by the manufacturer.

    Drug: SR-A + Epratuzumab

  • No intervention
    SR-B

    Patients randomized to the SR-B Arm receive induction, post-induction and maintenance therapy according to the protocol ALL-R3. In this arm patients are randomized not to receive epratuzumab. This randomization has been stopped pre-term on 1.2.2019 since the investigational product is not provided anymore by the manufacturer.

  • Active comparator
    SR-B + Epratuzumab

    Patients randomized to the SR-B Arm receive induction, post-induction and maintenance therapy according to the protocol ALL-R3. In this arm patients are randomized to receive epratuzumab. This randomization has been stopped pre-term on 1.2.2019 since the investigational product is not provided anymore by the manufacturer.

    Drug: SR-B + Epratuzumab

Interventions

  • DrugSR-A + Epratuzumab

    Also known as: Epratuzumab

  • DrugSR-B + Epratuzumab

    Also known as: Epratuzumab

06

What researchers measure

Primary outcomes

  1. SR induction/consolidation ALL-REZ BFM 2002 versus UK-ALL-R3 (randomisation 1)

    SR induction/consolidation ALL-REZ BFM 2002 versus UK-ALL-R3 (randomisation 1): 10% pEFS superiority of arm B above a 65% pEFS at 4 years of arm A

    Time frame: Up to 9 years

  2. SR consolidation +/- epratuzumab (randomisation 2)

    SR consolidation +/- epratuzumab (randomisation 2): 10% pEFS superiority of the arm with epratuzumab above an expected 74% pEFS at 4 years of the standard arm

    Time frame: Up to 9 years

Secondary outcomes

  1. SR induction/consolidation

    SR induction/consolidation: comparison of OS, toxicity, rate of CR2, and rate of MRD between treatment groups

    Time frame: Up to 9 years

  2. SR consolidation +/- epratuzumab

    SR consolidation +/- epratuzumab: comparison of OS, toxicity, MRD levels, rate of MRD and evaluation of pharmacokinetic parameters of Epratuzumab

    Time frame: Up to 9 years

07

Study locations

17 sites
  • Australian & New Zealand Childhood Hematology & Oncology Group
    Clayton, Victoria 3168, Australia
  • St. Anna Kinderkrebsforschung, CCRI
    Vienna, 1090, Austria
  • Hòpital Universitaire des Enfants Reine Fabiola
    Bruxelles, 1020, Belgium
  • University Hospital Motol
    Prague, Czechia
  • Copenhagen University Hospital (Rigshospitalet)
    Copenhagen, 2100, Denmark
  • Turku University Central Hospital
    Turku, SF-20520, Finland
  • CHU Nice
    Nice, France
  • Charité - Universitätsmedizin Berlin
    Berlin, 13353, Germany
  • Tel Aviv Sourasky Medical Centre
    Tel Aviv, 64239, Israel
  • Ospedale Pediatrico Bambino Gesù
    Roma, 00165, Italy
  • St.Lukes International Hospital
    Tokyo, Japan
  • Prinses Máxima Centrum, Lundlaan
    Utrecht, Netherlands
  • Oslo University Hospital
    Oslo, 0027, Norway
  • Dpt. SCT and Hematology/Oncology University Wroclaw
    Wroclaw, 50354, Poland
  • Instituto Português de Oncologia de Lisboa
    Lisboa, Portugal
  • University Children's Hospital Zurich
    Zürich, 8032, Switzerland
  • Royal Manchester Children's Hospital
    Manchester, M13 9WL, United Kingdom
08

References and documents

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 9, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT01802814
Lead sponsor
Charite University, Berlin, Germany
Collaborators
Australian & New Zealand Children's Haematology/Oncology Group, St. Anna Kinderkrebsforschung (Co-Sponsor Austria), European Organisation for Research and Treatment of Cancer - EORTC, University Hospital Motol (Co-Sponsor Czech Republic), Copenhagen University Hospital (Rigshospitalet) (Co-Sponsor Copenhagen), Turku University (Co-Sponsor Finland), Centre Hospitalier Universitaire de Nice, Our Lady's Chilrden's Hospital (Co-Sponsor Ireland), Tel Aviv Sourasky Medical Centre (Co-Sponsor Israel), Ospedale Pediatrico Bambino Gesù (Co-Sponsor Italy), National Hospital Organization Nagoya Medical Center (Co-Sponsor Japan), Prinses Máxima Centrum (Co-Sponsor Netherlands), Oslo University Hospital (Co-Sponsor Oslo), Medical University of Wroclaw (Co-Sponsor Poland), Instituto Português de Oncologia de Lisboa (Co-Sponsor Lisboa), Spanish Society of Pediatric Hematology and Oncology (SEHOP) (Co-Sponsor Spain), University Children's Hospital, Zurich, Central Manchester University (Co-Sponsor United Kingdom)
Responsible party
PD Dr. Arend von Stackelberg (PD Dr. med. Arend von Stackelberg, Charite University, Berlin, Germany) — Principal investigator
First posted
Mar 1, 2013
Start date
May 2014
Primary completion
Jul 31, 2023
Completion
Jul 31, 2023
Last update
Feb 9, 2024

Study contacts

Arend von Stackelberg, MD
principal investigator · University Hospital of Berlin - Charité

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Feb 2024. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion