International Chronic Myeloid Leukemia Pediatric Study (ICMLPed)

January 12, 2024 updated by: Poitiers University Hospital

INTERNATIONAL STUDY of Chronic Myeloid Leukaemia (CML) Treatment and Outcomes in Children and Adolescents

The purpose of the study is to describe and characterize CML in a large pediatric cohort of patients.

Study Overview

Status

Recruiting

Conditions

Detailed Description

International study of CML in children and adolescents

  1. Rational and objectives 1.1 Rational: Chronic myeloid leukaemia (CML) is a malignant disease of the hematopoietic system characterized by the presence a reciprocal translocation between chromosome 9 and 22. CML is a very rare disease in children and adolescents, accounting for 2% to 3% of leukemias in this age range, with an annual incidence of 1 case per million children (1,2,3). A recent report of the French National Registry of childhood leukemia and lymphoma revealed an incidence of 0.6 case per million children under 15 years of age between 1990 and 1999 in France. Characteristics of CML seem to differ in this age range compared with adults (5). In Europe, very few children and adolescents with CML is included in national trials nor are they recorded in regional or national registries. A European CML-Registry was established to improve the knowledge concerning this disease but only patients aged 18 years and over are registered. In Europe, a national registry was recently set up in UK to collect prospectively data in patients less than 15 years of age with CML. However, limited information is available concerning the epidemiology and the characteristics of CML in childhood.

    There are currently two main treatment options in children with CML. The first option is allogeneic hematopoietic transplantation which is a potentially curative therapy in children with a suitable donor. Transplantation with a matched unrelated donor resulted in an overall survival rate of 66% at 3 years in children with CML in first chronic phase (6). A 5-year overall survival rate of 73 % was reported in those transplanted with a matched sibling donor (7). The second option is treatment with imatinib mesylate, an orally administered antityrosine kinase. Imatinib mesylate is well tolerated and cytogenetic and molecular remissions can be achieved in a significant percentage of children with CML (8, 9). However, the ability of imatinib mesylate to cure the disease remains unknown.

    In adults with CML, Sokal and Hasford reported 2 distinct staging systems able to distinguish patient groups with different survival. These scoring systems were determined in cohorts of patients including adults and children, but the data of the younger patients were not analysed separately. Moreover, the Sokal score was determined in patients treated with busulfan or hydroxyurea and the Hasford score in patients receiving IFN therapy. Identification of prognosis factors and determination of a prognostic scoring system in children and adolescents with CML are essential to optimize individual treatment strategy in this age group. All these points justify the need for an international network to better describe this rare disease in children and adolescents and to optimize individual treatment strategy.

    1.2 Objectives.

    The main objectives of the study are the followings:

    • To describe the characteristics of CML in a large cohort of patients less than 18 years of age
    • To describe the treatment policies.
    • To identify prognostic factors in this age-group
    • To determine prognostic scoring systems in this population in order to optimize individual treatment choices.
    • To determine side effects and long term effects of treatments, mainly the tyrosine kinase inhibitor effect, on growth and development of a pediatric population

  2. Population. All patients less than 18 years of age with newly diagnosed Philadelphia positive and/or bcr-abl positive CML are eligible whatever the phase of the disease, the type of treatment and the enrollment or not in a clinical study.

    However their data will be collected only if requirements concerning ethics and policy agreement are fulfilled (see section 9)

  3. Method The study is strictly observational. Retrospective and prospective data will be collected from patient flow charts and/or existing databases.

    A steering committee (SC) including A Biondi, E De Bont, MF Dresse, J de la Fuente, M Suttorp, J Guilhot and F Millot will promote the international study of CML in children and adolescents. The SC will include representatives of each country involved in the study. The SC will agree on policy, support its implementation, initiate research, and raise public awareness about the study by presentations and publications.A scientific committee (SciC) will be set up. By laws regarding data property,analysis and publication will be decided by the scientific committee and the steering committee. For each objective of the study, there will be a working party (WP),which will be open to all interested participants in the study.Data will be provided by clinicians and biologists involved in pediatric haematology.The data base of the study will be set up in the Clinical Investigation Center(CIC INSERM 802)of the University Hospital of Poitiers(France)which will be the International Central Data Center(ICDC) of the study in charge of and centralizing the data. Sophie Zin Ka Yeu will be the responsible for the monitoring,E Ducasse for data base management and J Guilhot for the statistical analysis. The study is international.A National Coordinating Center and a leader will be identified in each participating country. The National Coordinating Center will be in charge of collecting data for his country. Each leader of the National Coordinating Center will be in charge of registering the patients and sending the data to the ICDC (CIC INSERM 802, Poitiers, France). To avoid double entry, the location of the medical center where the CML of the patient was diagnosed will be recorded in the case report form. Moreover, notification of new cases may be cross checked by national coordinators with their own national registry when available (for example with the Registre national des hémopathies malignes de l'enfant in France).

  4. Origin and type of data:

    Data will include:

    • Identification number
    • Demographic data
    • Date of birth
    • Sex
    • Medical data Ethnicity will be collected because of variation in terms of clinical characteristics (height for example) and pharmacokinetic of medication of the different groups of children potentially involved. Identifying biological results will not be collected.

    The ICDC will collect only data which is strictly anonymized by the national coordinating centers. Patients will be identified by a code including 2 to 3 letters for the country and 4 digits for the patient number (ex: FR/0001 for the first registered Patient in France). No initial of patients will be used. As country coordinator for France, F Millot will also collect initials of French patients in order to avoid double registration. These initials will not be computerized. The international ID number will be immediately provided.

  5. Circulation of the data The data is centralized in the ICDC of the study. The ICDC is located in the Clinical Research Investigation Center of the University Hospital of Poitiers (France).

    Retrospective data:the data will be collected in a one step procedure. Prospective data:The data will be collected using a two step procedures.

    1. Notification of the cases:

      New cases will be notified by physicians and biologists involved in pediatric hematology to their National Coordinating Center; at regular intervals these cases will then be referred by this coordinating center to the ICDC.

    2. Full data collection:

    The data will be collected from the clinical chart of the patients. The complete data will be send to each National Coordinating Center and then centralized at regular intervals subsequently in the ICDC. Follow up will be required twice a year. For each case of CML, a yet to be fixed sum of money will be transferred from the ICDC to the National Coordinating Center at notification of the case and when complete data transfer will be performed.

    To avoid extra work, data already computerized will be accepted if it fulfilled the requirements of ethics, confidentiality and partnership rules as mentioned in paragraph 7.

    When available agreement between parties, data may come from case report form of patients included in clinical studies or other Registries. Data will be sent by regular mail, fax or electronic file by the national coordinators to the ARC of the study at the ICDC. Data received by mail will be transferred by copy using disks (CD-Rom or external disk) to the data-manager and destroyed from the computer with mail box. Data will be entered in a Microsoft ACCESS database in the ICDC. Data base will be implemented in a PC (I) (Windows) located in a room dedicated for the purpose of the work. A second PC (II) in the same place will be used for duplication, backup, quality control and analysis of the data. None of these 2 PCs will offer connections such as Internet, or Intranet. The use of an electronic case Report form (e-CRF) is not planned. A secure access building and rooms of the ICDC is organized; specific password and login for the computers are used. At regular interval a secure storage of the data will be performed and located in the secure IDCD room organized for this purpose. Access to the data will be restricted to the coordinator of the study, the ARC, the data manager, the biostatistician, and Health Authorities, if needed.

  6. Study duration and organization The expected start date is August 1, 2009. The planned study duration is about 5 years. Study prolongation will depend on the funding linked to the effective participation of the centres in the study.

  7. Analysis of the data Data will be analysed using mainly SAS software (SAS institute, CARY, NC, USA). Final analyses will be provided within 5 years from start of the study. Analysis will be mainly descriptive. Date of inclusion in the study is defined as the date of reception of the notification of case by the ICDC. For the purpose of descriptive analysis, all parameters will be analysed at regular intervals: number of registered cases, baseline characteristics, follow-up and outcome variables. Categorical data will be presented with frequency, percentage and 95 % confidence interval. Quantitative variable will be presented with median and range, mean and standard deviation when relevant. Survival data and issue to events (time to response or side-effects, loss and duration of response…); will be analysed by the Kaplan Meier and competing risks methods. For prognosis factors identification, exploratory analyses will be performed as appropriate. The final statistical plan will be validated by the steering committee and the scientific committee.

    Reports will be provided every 6 months and by the end of the study by the ARC, the data manager, the biostatistician and Dr F. Millot, coordinator of the study. These reports will be sent to the national coordinators and to the participants. Results could be presented in Workshops, meetings and could be published with the agreement of the steering and scientific committees. All reports and publications will remain anonymous.

  8. Number of Patients :

    A proximately 100 to 150 patients per year are expected. As the number of cases of children and adolescent with CML being low, no strict calculation was made. The objective is to collect a maximum of cases to improve the power of the study.

  9. Ethical Considerations The children, according to their age, and their parents will be informed about the study and its procedures, according to the European policy regarding collection and transfer data for research purpose. Informed consent (parents and, when possible, children) will have to be provided.

Anonymized data will be collected and presented in this study. Rules will be in accordance with the Principles and Guideline of the European Community concerning clinical studies and data collection and the French Law "Informatique, fichiers et liberté" (January 6, 1978, updated.It is the responsibility of each national coordinator to provide insurance concerning the participation of the members of his groups according these rules and the local rules required by his own country.

Study Type

Observational

Enrollment (Estimated)

750

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

  • Australia
    • South Australia
      • North Adelaide, South Australia, Australia, 5006
        • Not yet recruiting
        • Women's and Children's Hospital
        • Contact:
        • Principal Investigator:
          • Heather TAPP, MD
  • Austria
      • Vienna, Austria, 1090
        • Recruiting
        • St. Anna Children's Cancer Research Institute and St. Anna Children's Hospital
        • Principal Investigator:
          • Michael DWORZAK, MD
        • Contact:
  • Belarus
      • Minsk, Belarus
        • Recruiting
        • Belarussian Reseach Center for Pediatric Oncology and hematology (BRCPOH)
        • Contact:
        • Contact:
        • Sub-Investigator:
          • Natalia SAVVA, MD
        • Principal Investigator:
          • Marina BORISEVICH
  • Belgium
      • Ghent, Belgium, 9000
        • Recruiting
        • University Hospital of Ghent
        • Contact:
        • Sub-Investigator:
          • Marie Françoise DRESSE, MD
        • Principal Investigator:
          • Barbara DE MOERLOOSE, PhD
        • Sub-Investigator:
          • Alina FERSTER
        • Sub-Investigator:
          • Marlies BEKAERT
  • Brazil
      • Sao Paulo, Brazil, 04023-062
        • Recruiting
        • Instituto De Oncologia Pediatrica
        • Contact:
        • Contact:
        • Principal Investigator:
          • Silvia Regina BRANDALISE, MD
        • Sub-Investigator:
          • Julia YAJIMA
  • Chile
      • Santiago, Chile
        • Not yet recruiting
        • Hospital Roberto del Rio
        • Contact:
        • Contact:
        • Sub-Investigator:
          • Myriam CAMPBELL BULL, MD
        • Principal Investigator:
          • Paulina DIAZ
        • Sub-Investigator:
          • Monica VARAS PALMA
  • China
      • Hong Kong, China
        • Recruiting
        • Prince of Wales Hospital
        • Contact:
        • Sub-Investigator:
          • Li CHI KONG, MD
        • Principal Investigator:
          • Frankie CHENG
  • Croatia
      • Zagreb, Croatia
        • Recruiting
        • Children's Hospital Zagreb
        • Contact:
        • Principal Investigator:
          • Gordana JAKOVLJEVIC
  • Czechia
      • Prague, Czechia
        • Recruiting
        • Charles University Motol
        • Contact:
        • Contact:
        • Principal Investigator:
          • Petr SEDLACEK, PHD
        • Sub-Investigator:
          • Petr SMISEK
  • Denmark
      • Copenhagen, Denmark, 2100
        • Recruiting
        • Rigshospitalet
        • Contact:
        • Principal Investigator:
          • Birgitte LAUSEN, MD
  • France
      • Poitiers, France, 86021
        • Recruiting
        • Clinical Investigation Center CIC 1402
        • Contact:
        • Principal Investigator:
          • Frédéric MILLOT, MD
  • Germany
  • Greece
      • Athen, Greece, 11527
        • Recruiting
        • Agia Sophia Children's Hospital
        • Contact:
        • Contact:
        • Principal Investigator:
          • Mirella AMPATZIDOU, PhD
        • Sub-Investigator:
          • Sophia POLYCHRONOPOULOU
  • Japan
      • Tokyo, Japan, 160-8582
        • Not yet recruiting
        • Keio University School of Medicine
        • Contact:
        • Contact:
        • Principal Investigator:
          • HIROYUKI Shimada, MD PhD
        • Sub-Investigator:
          • Shima HARUKO
  • Lebanon
      • Beirut, Lebanon
        • Recruiting
        • Saint George Hospital University Medical Centre
        • Contact:
        • Principal Investigator:
          • Farah ROULA
  • Netherlands
      • Utrecht, Netherlands
        • Recruiting
        • Dutch Childhood Oncology Group, Princess Maxima Center for pediatric oncology
        • Contact:
        • Principal Investigator:
          • Maaike LUESINK, MD
  • Poland
      • Wrocław, Poland
        • Recruiting
        • Wroclaw Medical University Department
        • Contact:
        • Contact:
        • Principal Investigator:
          • Krzysztof KALWAK, PhD
  • Slovakia
      • Bratislava, Slovakia, 813 72
        • Recruiting
        • University Children's Hospital
        • Contact:
        • Sub-Investigator:
          • Andrea HRASKOVA
        • Contact:
        • Principal Investigator:
          • Alexandra KOLENOVA, MD
  • Spain
  • Turkey
      • Görükle, Turkey
        • Recruiting
        • Uludag University, Medical Faculty
        • Contact:
        • Principal Investigator:
          • Adalet M GÜNEŞ, MD

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

No older than 18 years (Child, Adult)

Accepts Healthy Volunteers

No

Sampling Method

Non-Probability Sample

Study Population

All patients less than 18 years of age with newly diagnosed Philadelphia positive and/or bcr-abl positive CML are eligible whatever the phase of the disease, the type of treatment and the enrollment or not in a clinical study.

Description

Inclusion Criteria:

  • patients less than 18 years of age
  • diagnosed Philadelphia positive and/or BCR-ABL positive Chronic Myeloid Leukemia (CML) all phases

Exclusion Criteria:

  • patients more than 18 years of age at diagnosis of CML

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Poitiers University Hospital

Collaborators

University Medical Center Groningen
Imperial College London
University of Liege
University of Milano Bicocca
University Hospital Dresden
International BFM Study Group
CIC Inserm 1402

Investigators

  • Principal Investigator: Frederic MILLOT, MD, Poitiers University Hospital

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

January 1, 2011

Primary Completion (Estimated)

December 1, 2028

Study Completion (Estimated)

December 1, 2028

Study Registration Dates

First Submitted

January 14, 2011

First Submitted That Met QC Criteria

January 20, 2011

First Posted (Estimated)

January 24, 2011

Study Record Updates

Last Update Posted (Actual)

January 17, 2024

Last Update Submitted That Met QC Criteria

January 12, 2024

Last Verified

January 1, 2024

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • CIC1402
  • 2010-023359-27 (EudraCT Number)

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

Clinical Trials on Chronic Myeloid Leukemia

Search Similar Trials

Sponsors and Collaborators

Medical Conditions

Drug Interventions

CROs by country

CROs in Mongolia

Conditions

Rare Diseases

Drug Interventions

Dietary Supplements

Sponsor/Collaborators

Locations

Subscribe