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Graft Composition

Differences between graft product and donor side effects following bone marrow or stem cell donation

Summary:

We report graft product stem cell yields and donor safety results of a randomized multicenter study comparing allogeneic peripheral blood stem cell (PBSC) PBSC transplantation with BM transplantation. Matched HLA-identical sibling donors (n=329) were randomized to filgrastim-mobilized PBSC or bone marrow (BM) donation groups. Median yields per kg recipient weight of CD34+ cells, T cells, and natural killer (NK) cells, respectively, were approximately two-fold, eight-fold, and greater than eight-fold in the PBSC group than in the BM group (CD34+ cells, 5.8 × 106/kg vs 2.7 × 106/kg; T cells, 300.1 × 106/kg vs 35.7 × 106/kg; NK cells, 28.2 × 106/kg vs 3.6 × 106/kg; P<0.001 for each). In connection with the cell collection procedures, PBSC donors spent a shorter median time in hospital than BM donors (0 vs 2 days; median difference −2 days, 95% CI −2 to 2) and had fewer median days of restricted activity (2 vs 6 days; median difference −3 days, 95% CI −4 to 2). Overall, 65% of PBSC donors and 57% of BM donors reported at least one adverse event (AE), most of which were transient, mild–moderate in severity, and without clinical sequelae. PBSC donors experienced predominantly filgrastim-related AEs, while BM donors experienced predominantly harvest-related AEs.

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Acknowledgements

This study was sponsored by Amgen Ltd., Cambridge, UK, and F Hoffmann – La Roche AG, Basel, Switzerland, and partially supported by grants from the Swiss National Research Foundation (32-52756.97) and the Horton Foundation to Dr G Favre.

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Appendix

Appendix

This study was conducted at the following institutions under the auspices of the named principal investigators: Allgemeines Krankenhaus, Vienna, Austria (H Greinix); University Hospital, Innsbruck, Austria (D Niederwieser, D Nachbauer); University Hospital, Leuven, Belgium (M Boogaerts); Cliniques Universitaires St Luc, Brussels, Belgium (A Ferrant); Charité der Humboldt Universität, Berlin, Germany (R Arnold); Hôpital St Louis, Paris, France (E Gluckman); Hôpital St. Antoine, Paris, France (NC Gorin); Universität Ulm, Ulm, Germany (N Frickhofen); Christian-Albrechts Universität, Kiel, Germany (N Schmitz); Universitätsklinikum Eppendorf, Hamburg, Germany (A Zander); St James Hospital, Dublin, Ireland (S McCann); Hadassah University Hospital, Jerusalem, Israel (A Nagler); Ospedale San Martino, Genova, Italy (A Bacigalupo); Kantonsspital Basel, Basel, Switzerland (A Gratwohl); Hammersmith Hospital, London, UK (J Apperley); Nottingham City Hospital, Nottingham, UK (NH Russell); Huddinge Hospital, Huddinge, Sweden (O Ringdén); Ospedale V Cervello-USL, Palermo, Italy(I Majolino); Hôpital Claude Huriez, Lille, France (JP Jouet); Hôpital Necker, Paris, France (B Varet); Klinikum der Albert-Ludwigs Universität, Freiburg, Germany (J Finke); Leeds General Infirmary, Leeds, UK (G Smith); Azienda Ospedaliera Careggi, Firenze, Italy (A Bosi); Padiglione G Marcora, Ospedale Maggiore di Milano, Milano, Italy (G Lambertenghi-Deliliers); Universitätsklinikum, Mainz, Germany (K Kolbe); Helsinki University Central Hospital, Helsinki, Finland (T Ruutu); Westmead Hospital, Westmead, Australia (KA Bradstock); LCHRU de Hautepierre, Strasbourg, France (B Lioure); Hanson Centre for Cancer Research, Royal Adelaide Hospital, Adelaide, Australia (T Hughes); Royal Melbourne Hospital, Parkville, Australia (J Szer); Royal Perth Hospital, Perth, Australia (R Herrmann); Universitätsklinik, Hamburg, Germany (L Trümper); Centro Dipartimentale Trapianti di Midollo, Ospedale Molinette, Torino, Italy (M Falda); Ankara University Medical Facility, Ankara, Turkey (M Beksaç); Evangelismos General Hospital, Athens, Greece (E Nikiforakis); Instituto Portugues de Oncologia Francisco Gentil, Lisbon, Portugal (M Abecasis); Rambam Medical Center, Haifa, Israel (J Rowe); Royal Free Hospital, Hampstead, London, UK (M Potter); Medizinische Klinik Nürnberg, Nürnberg, Germany (H Wandt); Stiftung Deutsche Klinik f. Diagnostik, Wiesbaden, Germany (R Schwerdtfeger); Universität Rostock, Rostock, Germany (J Casper); King's College Hospital, London, UK (A Pagliuca).

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Favre, G., Beksaç, M., Bacigalupo, A. et al. Differences between graft product and donor side effects following bone marrow or stem cell donation. Bone Marrow Transplant 32, 873–880 (2003). https://doi.org/10.1038/sj.bmt.1704245

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