Abstract
Donor T-cells transferred after allogeneic stem cell transplantation (alloSCT) can result in long-term disease control in myeloma by the graft-versus-myeloma (GvM) effect. However, T-cell therapy may show differential effectiveness against bone marrow (BM) infiltration and focal myeloma lesions resulting in different control and progression patterns. Outcomes of 43 myeloma patients who underwent T-cell-depleted alloSCT with scheduled donor lymphocyte infusion (DLI) were analyzed with respect to diffuse BM infiltration and focal progression. For comparison, 12 patients for whom a donor search was started but no alloSCT was performed, were analyzed. After DLI, complete disappearance of myeloma cells in BM occurred in 86% of evaluable patients. The probabilities of BM progression-free survival (PFS) at 2 years after start of donor search, alloSCT and DLI, were 17% (95% confidence interval 0–38%), 51% (36–66%), and 62% (44–80%) respectively. In contrast, the probabilities of focal PFS at 2 years after start of donor search, alloSCT and DLI, were 17% (0–38%), 30% (17–44%) and 28% (11–44%), respectively. Donor-derived T-cell responses effectively reduce BM infiltration, but not focal progression in myeloma, illustrating potent immunological responses in BM with only limited effect of T-cells on focal lesions.
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Acknowledgements
This work was supported by research grant 2008-4263 from the Dutch Cancer Society, Amsterdam, The Netherlands. We thank Illyea Hawke (DKMS, Germany) for correcting the language of the manuscript.
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Eefting, M., de Wreede, L., Von dem Borne, P. et al. Donor T-cell responses and disease progression patterns of multiple myeloma. Bone Marrow Transplant 52, 1609–1615 (2017). https://doi.org/10.1038/bmt.2017.201
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DOI: https://doi.org/10.1038/bmt.2017.201
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