Author: Julia Dobke, erstellt 2005/02/12, Last modification: 2018/10/24

Title ALCL-Relapse: Treatment protocol for relapsed anaplastic large cell lymphoma of childhood and adolescence
Disease Relapsed anaplastic large cell lymphoma of childhood and adolescence
Type An European Inter-group Cooperation on Childhood Non-Hodgkin Lymphoma (EICNHL) International Multicentre Therapy Study
Problem / Objectives

Prymary objectives

  • to improve the probability of event free survival in children and adolescents with early progression of ALCL or/and a relapse of ALCL with CD3 positive immunophenotype
  • to test whether in patients with relapse of CD3 negative ALCL occurring after the intensive phase of frontline treatment BEAM conditioning regimen (without TBI) for autologous stem cell transplantation is an effective treatment
  • to test the impact of Vinblastine in patients with late relapse of an CD3 negative ALCL
Therapy / Study arms


  • Timepoint of the relapse
  • Immunophenotype of the ALCL
  • Availability of MSD or 10/10 MUD Sc-donor
  • Vinblastine administration during frontline therapy

Classification of therapeutic groups

  • Arm 1: Early progression
  • Arm 2: Relapse and CD3 positive lymphoma cells: Arm 2a: a matched sibling donor or a 10/10 matched non-sibling donor is available; Arm 2b: no matched sibling donor or a 10/10 matched non-sibling donor available
  • Arm 3: Relapse and CD3 negative immunophenotype
  • Arm 4: Late relapse and CD3 negative immunophenotype
Inclusion Criteria
  • progression or relapse of ALCL
  • age < 22 years
  • slides of relapsed lymphoma available for national pathological and/or cytomorphology review
  • signed informed consent of patient/guardians for participation in the study ALCL-Relapse
  • no evidence of pregnancy or lactation period; assured contraception
  • no participation in another clinical study, recruitment in study ALCLRelapse during run time of the study

Patients who fulfil the eligibility criteria of the study but who meet one of the following criteria are not evaluable for trial’s results. Nevertheless, they should be registered and documented in the study.

Exclusion Criteria
  • 2nd, or subsequent relapse of ALCL
  • significant pre-treatment for 1st relapse
  • no adequate hepatic, renal and cardiac function
  • HIV infection or AIDS, severe immunodeficiency
  • previous organ transplantation
  • previous malignancy prior to the anaplastic large cell lymphoma
  • pre-existing disease prohibiting treatment as per instruction of protocol
Status Start: April 2004
Principal Investigator Prof. Dr. med. Alfred Reiter


Prof. Dr. Dr. Birgit Burkhardt
Universitätsklinikum Münster
Klinik und Poliklinik für Kinder- und Jugendmedizin, Pädiatrische Hämatologie und Onkologie
Albert-Schweitzer-Campus 1
48149 Münster
Telefon +49 (251) 83 55696
Fax +49 (251) 83 43405

Participants AIEOP: Associazione Italiana di Ematologia ed Oncologia Pediatrica BFM Austria, Czechia, Germany and Switzerland BSPHO: Belgian society of paediatric haematology/oncology DCOG: Dutch Childhood Oncology Group NOPHO: Nordic Society of Pediatric Haematology and Oncology PPLLSG: Polish Paediatric Leukaemia/Lymphoma Study Group SFCE: Société Française des Cancers de l'Enfant SHOP: Spanish Leukemia Group UKCCSG: United Kingdom Children Cancer Study Group
Link(s) Studienliteretaur zu den Non-Hodgkin-Lymphomen
Trial literature