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Volume 16, Issue 3, Pages 320-332 (March 2010)


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Partial T Cell-Depleted Allogeneic Stem Cell Transplantation following Reduced-Intensity Conditioning Creates a Platform for Immunotherapy with Donor Lymphocyte Infusion and Recipient Dendritic Cell Vaccination in Multiple Myeloma

Henriëtte Levenga1Corresponding Author Informationemail address, Nicolaas Schaap1, Frans Maas2, Bennie Esendam2, Hanny Fredrix2, Annelies Greupink-Draaisma2, Theo de Witte1, Harry Dolstra2, Reinier Raymakers1

Received 4 June 2009; accepted 7 October 2009. published online 15 October 2009.

Allogeneic stem cell transplantation (SCT) in multiple myeloma (MM) may induce a curative graft-versus-myeloma (GVM) effect. Major drawback in unmanipulated reduced-intensity conditioning (RIC) SCT is the risk of severe and longstanding graft-versus-host-disease (GVHD). This study demonstrates that transplantation with a partial T cell-depleted graft creates a platform for boosting GVM immunity by preemptive donor lymphocyte infusion (DLI) and recipient dendritic cell (DC) vaccination, with limited GVHD. All 20MM patients engrafted successfully. Chimerism analysis in 19 patients evaluable at 3 months revealed that 7 patients were complete donor, whereas 12 patients were mixed chimeric. Grade II acute GVHD (aGVHD) occurred in 7 patients (35%) and only 4 patients (21%) developed chronic GVHD (cGVHD). Fourteen patients received posttransplantation immunotherapy, 8 preemptive DLI, 5 patients both DLI and DC vaccination, and 1 patient DC vaccination only. DC vaccination was associated with limited toxicity, and none of these patients developed GVHD. Importantly, overall treatment-related mortality (TRM) at 1 year was low (10%). Moreover, the overall survival (OS) is 84% with median follow-up of 27 months, and none of the patients died from progressive disease. These findings illustrate that this novel approach is associated with limited GVHD and mortality, thus creating an ideal platform for adjuvant immunotherapy.

1 Department of Hematology, Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands

2 Central Hematology Laboratory, Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands

Corresponding Author InformationCorrespondence and reprint requests: Henriëtte Levenga, MD, Department of Hematology, Radboud University Nijmegen Medical Centre, Geert Grooteplein 8, P.O. Box 9101, 6500 HB Nijmegen, The Netherlands.

 Financial disclosure: See Acknowledgments on page 332.

PII: S1083-8791(09)00462-5

doi:10.1016/j.bbmt.2009.10.006


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