Peripheral Blood (PB) Versus Bone Marrow (BM) in Allogeneic Stem Cell Transplantation

NCT01020175 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 350

Last updated 2009-11-25

No results posted yet for this study

Summary

350 patients with early leukemias were assigned to receive peripheral blood or bone marrow transplantation; the occurrence of acute and chronic graft versus host disease, survival, transplantation-related mortality, and relapse rates were compared.

Conditions

Interventions

PROCEDURE

Bone marrow transplantation

Patients received bone marrow transplantation

PROCEDURE

Peripheral blood stem cell transplantation

Patients received filgrastim-mobilized peripheral blood stem cell transplantation

Sponsors & Collaborators

  • Amgen

    collaborator INDUSTRY
  • Hoffmann-La Roche

    collaborator INDUSTRY
  • European Society for Blood and Marrow Transplantation

    lead NETWORK

Principal Investigators

  • Nobert Schmitz, Prof. · Christian-Albrechts- Universita¨t, Kiel, Germany

  • H Greinix, Dr · Allgemeines Krankenhaus, Vienna, Austria

  • D Niederwieser, Dr · University Hospital Innsbruck, Austria

  • M. Boogaerts, Dr. · University Hospital, Leuven, Belgium

  • A Ferrant, Dr · Cliniques Universitaires St Luc, Brussels, Belgium

  • R. Arnold, Dr. · Charite der Humboldt Universität, Berlin, Germany

  • E Gluckman, Dr. · Hopital St Louis, Paris, France

  • N C Gorin, Dr. · Hoˆpital St Antoine, Paris, France

  • N Frickhofen, Dr · Universita¨t Ulm, Germany

  • P Dreger, Dr. · Christian-Albrechts- Universita¨t, Kiel, Germany

  • A Zander, Dr · Universitätsklinikum Eppendorf, Hamburg, Germany

  • S McCann, Dr. · St James Hospital, Dublin, Ireland

  • A Nagler, Dr. · Hadassah University Hospital, Jerusalem, Israel

  • A Bacigalupo, Dr. · Ospedale San Martino, Genova, Italy

  • A Gratwohl, Dr. · Kantonsspital, Basel, Switzerland

  • J Apperley, Prof. · Hammersmith Hospital, London, United Kingdom

  • N H Russell, Dr. · Nottingham City Hospital, United Kingdom

  • O Ringde´n, Dr. · Huddinge Hospital, Sweden

  • I Majolino, Dr. · Ospedale V Cervello-USL, Palermo, Italy

  • J P Jouet, Dr. · Hopital Claude Huriez, Lille, France

  • B Varet, Dr. · Hopital Necker, Paris, France

  • J Finke, Dr. · Klinikum der Albert-Ludwigs-Universität, Freiburg, Germany

  • G. Smith, Dr. · Leeds General Infirmary, United Kingdom

  • A Bosi, Dr. · Azienda Ospedaliera Careggi, Firenze, Italy

  • G Lambertenghi-Deliliers, Dr. · Padiglione G Marcora, Ospedale Maggiore di Milano, Italy

  • K Kolbe, Dr. · Universitatsklinikum, Mainz, Germany

  • T Ruutu, Dr. · Helsinki University CT. Rentral Hospital, Finland

  • K A Bradstock), Dr. · Westmead Hospital, Australia

  • B Lioure, Dr. · LCHRU de Hautepierre, Strasbourg, France

  • T Hughes, Dr. · Hanson Centre for Cancer Research, Royal Adelaide Hospital, Australia

  • J Szer, Dr. · Royal Melbourne Hospital, Parkville, Australia

  • R Herrmann, Dr. · Royal Perth Hospital, Australia

  • L Tru¨mper, Dr. · Universitätsklinik, Homburg, Germany

  • M Falda, Dr. · Centro Dipartimentale Trapianti di Midollo, Ospedale Molinette, Torino, Italy

  • M Beksac, Dr. · Ankara University Medical Facility, Turkey

  • E Nikiforakis, Dr. · Evangelismos General Hospital, Athens, Greece

  • M Abecasis, Dr. · Instituto Portugues de Oncologia Francisco Gentil, Lisboa, Portugal

  • J Rowe, Dr. · Rambam Medical Center, Haifa, Israel

  • M Potter, Dr. · Royal Free Hospital Hampstead, London, United Kingdom

  • H Wandt, Dr. · Medizinische Klinik Nurnberg, Germany

  • R Schwerdtfeger, Dr. · Stiftung Deutsche Klinik f. Diagnostik, Wiesbaden, Germany

  • J Casper, Dr · University Rostock, Germany

  • A. Pagliuca, Dr. · King's College Hospital, London, United Kingdom

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
55 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
1995-01-31
Primary Completion
1999-12-31
Completion
2002-12-31

Countries

  • Germany

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01020175 on ClinicalTrials.gov